WO2004098591A2 - Inhibitors of glutaminyl cyclase and their use in the treatment of neurological diseases - Google Patents

Inhibitors of glutaminyl cyclase and their use in the treatment of neurological diseases Download PDF

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WO2004098591A2
WO2004098591A2 PCT/EP2004/004773 EP2004004773W WO2004098591A2 WO 2004098591 A2 WO2004098591 A2 WO 2004098591A2 EP 2004004773 W EP2004004773 W EP 2004004773W WO 2004098591 A2 WO2004098591 A2 WO 2004098591A2
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independently
carbocycle
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PCT/EP2004/004773
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French (fr)
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WO2004098591A3 (en
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Hans-Ulrich Demuth
Ulrich Heiser
Mirko Buchholz
André J. NIESTROJ
Stephan Schilling
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Probiodrug Ag
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Priority to AT04731158T priority Critical patent/ATE462432T1/en
Priority to DE602004026289T priority patent/DE602004026289D1/en
Priority to EP04731158A priority patent/EP1620091B1/en
Priority to JP2006505375A priority patent/JP4806628B2/en
Publication of WO2004098591A2 publication Critical patent/WO2004098591A2/en
Publication of WO2004098591A3 publication Critical patent/WO2004098591A3/en

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    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
    • C07F9/572—Five-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
    • C07F9/576—Six-membered rings
    • C07F9/59—Hydrogenated pyridine rings
    • C—CHEMISTRY; METALLURGY
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    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6503—Five-membered rings
    • C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Definitions

  • the invention relates to glutaminyi cyclase (QC, EC 2.3.2.5) that catalyzes the intramolecular cyclization of N-terminal glutamine residues into pyroglutamic acid (5- oxo-prolyl, pGlu * ) under liberation of ammonia and the intramolecular cyclization of N- terminal glutamate residues into pyroglutamic acid under liberation of water.
  • glutaminyi cyclase QC, EC 2.3.2.5
  • Glutaminyi cyclase catalyzes the intramolecular cyclization of N- terminal glutamine residues into pyroglutamic acid (pGlu * ) liberating ammonia.
  • pGlu * pyroglutamic acid
  • EP 02 011 349.4 discloses polynucleotides encoding insect glutaminyi cyclase, as well as polypeptides encoded thereby.
  • This application further provides host cells comprising expression vectors comprising polynucleotides of the invention. Isolated polypeptides and host cells comprising insect QC are useful in methods of screening for agents that reduce glutaminyi cyclase activity. Such agents are useful as pesticides.
  • DP IV-inhibitor or "dipeptidyl peptidase IV inhibitor” is generally known to a person skilled in the art and means enzyme inhibitors, which inhibit the catalytical activity of DP IV or DP IV-like enzymes.
  • DP IV-activity is defined as the catalytical activity of dipeptidyl peptidase IV (DP IV) and DP IV-like enzymes. These enzymes are post-proline (to a lesser extent post- alanine, post-serine or post-glycine) cleaving serine proteases found in various tissues of the body of a mammal including kidney, liver, and intestine, where they remove dipeptides from the N-terminus of biologically active peptides with a high specificity when proline or alanine form the residues that are adjacent to the N-terminal amino acid in their sequence.
  • DP IV dipeptidyl peptidase IV
  • DP IV-like enzymes are post-proline (to a lesser extent post- alanine, post-serine or post-glycine) cleaving serine proteases found in various tissues of the body of a mammal including kidney, liver, and intestine, where they remove dipeptides from the N-
  • PEP-inhibitor or "prolyl endopeptidase inhibitor” is generally known to a person skilled in the art and means enzyme inhibitors, which inhibit the catalytical activity of prolyl endopeptidase (PEP).
  • QC as used herein comprises glutaminyi cyclase (QC) and QC-like enzymes.
  • QC and QC-like enzymes have identical or similar enzymatic activity, further defined as QC activity.
  • QC-like enzymes can fundamentally differ in their molecular structure from QC.
  • QC activity is defined as intramolecular cyclization of N- terminal glutamine residues into pyroglutamic acid (pGlu * ) or of N-terminal L- homoglutamine or L- ⁇ -homoglutamine to a cyclic pyro-homoglutamine derivative under liberation of ammonia. See therefore schemes 1 and 2.
  • EC as used herein comprises the side activity of QC and QC-like enzymes as glutamate cyclase (EC), further defined as EC activity.
  • QC/EC refers to the glutaminyi cyclase, which has at least one of QC or EC activity, preferably both, QC and EC activity.
  • EC activity as used herein is defined as intramolecular cyclization of N- terminal glutamate residues into pyroglutamic acid (pGlu * ) by QC. See therefore scheme 3.
  • QC-inhibitor "glutaminyi cyclase inhibitor” is generally known to a person skilled in the art and means enzyme inhibitors, which inhibit the catalytical activity of glutaminyi cyclase (QC) and/or its glutamyl cyclase (EC) activity.
  • subject refers to an animal, preferably a mammal, most preferably a human, who has been the object of treatment, observation or experiment.
  • terapéuticaally effective amount means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue system, animal or human being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated.
  • the term "pharmaceutically acceptable” embraces both human and veterinary use: for example the term “pharmaceutically acceptable” embraces a veterinarily acceptable compound or a compound acceptable in human medicine a health care.
  • acyl can denote a C ⁇ -2 o acyl residue, preferably a C 1 -8 acyl residue and especially preferred a C -4 acyl residue;
  • cycloalkyl can denote a C 3-12 cycloalkyl residue, preferably a C 4 , C 5 or C 6 cycloalkyl residue;
  • a carbocycle can denote a C 3-12 a carbocycle residue, preferably a C 4 , C 5 or C ⁇ a carbocycle residue.
  • Heteroaryl is defined as an aryl residue, wherein 1 to 4, and more preferably 1 , 2 or 3 ring atoms are replaced by heteroatoms like N, S or O.
  • a heterocycle is defined as a cycloalkyl residue, wherein 1 , 2 or 3 ring atoms are replaced by heteroatoms like N, S or O.
  • Peptides are selected from dipeptides to decapeptides, preferred are dipeptides, tripeptides, tetrapeptides and pentapeptides. The amino acids for the formation of the "peptides” can be selected from those listed above.
  • alkyl can denote a C 1 - 50 alkyl group, preferably a C 6- 3o alkyl group, especially a C ⁇ - 12 alkyl group; for example, an alkyl group may be a methyl, ethyl, propyl, isopropyl or butyl group.
  • alk for example in the expression “alkoxy”, and the expression “alkan”, for example in the expression “alkanoyl”, are defined as for “alkyl”; aromatic compounds are preferably substituted or optionally unsubstituted phenyl, benzyl, naphthyl, biphenyl or anthracene groups, which preferably have at least 8 C atoms;
  • alkenyl can denote a C 2 -1 0 alkenyl group, preferably a C 2 -6 alkenyl group, which has the double bond(s) at any desired location and may be substituted or unsubstituted;
  • alkynyl can denote a C 2- ⁇ o alkynyl group, preferably a C 2-6 alkynyl group, which has the triple bond(s) at any desired location and may be substituted or unsubstituted.
  • substituted or substituent can denote any desired substitution by one or more, preferably one or two, alkyl, alkenyl, alkynyl, mono- or multi-valent acyl, alkanoyl, alkoxyalkanoyl or alkoxyalkyl groups; the afore-mentioned substituents may in turn have one or more (but preferably zero) alkyl, alkenyl, alkynyl, mono- or multi-valent acyl, alkanoyl, alkoxyalkanoyl or alkoxyalkyl groups as side groups; organic amines, amides, alcohols or acids, each having from 8 to 50 C atoms, preferably from 10 to 20 C atoms, can have the formulae (alkyl) 2 N- or alkyl-NH-, -CO-N(alkyl) 2 or -CO-NH(alkyl), - alkyl-OH or -alkyl-COOH.
  • substituted or “substituent” can denote one or two of each, branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle; the afore-mentioned substituents may in turn have one or more branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle as side group(s); all herein before mentioned chains, residues or side groups may contain one or more, preferably one or two, epoxy moiety(ies) and one or more, preferably one or two, substituted or unsubstituted aziridine(s), whereas the substitution is characterized again as R ⁇ which is described above; all chains, residues or
  • all afore-mentioned chains, residues or side groups may contain one or more, preferably one, two or three alcohol(s), acid(s), aldehyde(s) or ketone(s), phosphane(s), phosphorane(s), sulfoxides (SO), sulfones (S0 2 ), their selenium or tellurium analogues named selenoxide and selenone, sulfonic anhydride(s) [(S0 2 ) 2 ⁇ ] and sulphonic anhydride(s) [(SO)2 ⁇ ], hydrazide(s), ⁇ /-Oxides of azo compounds; as well as amine(s), amide(s), ester(s), ether(s) or sulfonamid(e), phosphane(s) or phosphorane(s), having the formulae -NHRi or -N(Ri) 2 , -CON(Ri) 2 or -(
  • Amino acids which can be used in the present invention are L and D-amino acids, N- methyl-amino acids, aza-amino acids; allo- and t ⁇ reo-forms of lie and Thr, which can, e.g. be ⁇ -, ⁇ - or ⁇ -amino acids, whereof ⁇ -amino acids are preferred.
  • amino acids are: aspartic acid (Asp), glutamic acid (Glu), arginine (Arg), lysine (Lys), histidine (His), glycine (Gly), serine (Ser), cysteine (Cys), threonine (Thr), asparagine (Asn), glutamine (Gin), tyrosine (Tyr), alanine (Ala), proline (Pro), valine (Val), isoleucine (lie), leucine (Leu), methionine (Met), phenylalanine (Phe), tryptophan (Trp), hydroxyproline (Hyp), beta-alanine (beta-Ala), 2-aminooctanoic acid (Aoa), acetidine-(2)-carboxylic acid (Ace), pipecolic acid (Pip), 3-aminopropionic acid, 4-aminobutyric acid and so forth, alpha- aminoisobutyric acid (As
  • t ⁇ -amino acids are e.g.: 5-Ara (aminoraleric acid), 6-Ahx (aminohexanoic acid), 8-Aoc (aminooctanoic aicd), 9-Anc (aminovanoic aicd), 10-Adc (aminodecanoic acid), 11-Aun (aminoundecanoic acid), 12-Ado (aminododecanoic acid).
  • amino acids are: indanylglycine (Igl), indoline-2-carboxylic acid (Idc), octahydroindole-2-carboxylic acid (Oic), diaminopropionic acid (Dpr), diaminobutyric acid (Dbu), naphtylalanine (1-Nal) and (2-Nal), 4-aminophenylalanine (Phe(4-NH 2 )), 4- benzoylphenylalanine (Bpa), diphenylalanine (Dip), 4-bromophenylalanine (Phe(4-Br)), 2-chlorophenylalanine (Phe(2-CI)), 3-chlorophenylalanine (Phe(3-CI)), 4- chlorophenylalanine (Phe(4-CI)), 3,4-chlorophenylalanine (Phe (3,4-C )), 3- fluorophenylalanine (Phe(3-F)),
  • Peptides are selected from dipeptides to decapeptides, preferred are dipeptides, tripeptides, tetrapeptides and pentapeptides.
  • the amino acids for the formation of the "peptides” can be selected from those listed above.
  • aza-amino acid is defined as an amino acid where the chiral ⁇ -CH group is replaced by a nitrogen atom
  • an “aza-peptide” is defined as a peptide, in which the chiral ⁇ -CH group of one or more amino acid residues in the peptide chain is replaced by a nitrogen atom.
  • Proteinogenic amino acids are defined as natural protein- derived ⁇ -amino acids.
  • Non-proteinogenic amino acids are defined as all other amino acids, which are not building blocks of common natural proteins.
  • Protein mimetics per se are known to a person skilled in the art. They are preferably defined as compounds which have a secondary structure like a peptide and optionally further structural characteristics; their mode of action is largely similar or identical to the mode of action of the native peptide; however, their activity (e.g. as an antagonist or inhibitor) can be modified as compared with the native peptide, especially vis a vis receptors or enzymes. Moreover, they can imitate the effect of the native peptide (agonist). Examples of peptide mimetics are scaffold mimetics, non-peptidic mimetics, peptoides, peptide nucleic acids, oligopyrrolinones, vinylogpeptides and oligocarbamates.
  • the compounds according to this invention may accordingly exist as enantiomers. Where the compounds possess two or more chiral centers, they may additionally exist as diastereomers. It is to be understood that all such isomers and mixtures thereof are encompassed within the scope of the present invention.
  • the processes for the preparation of the compounds according to the invention give rise to a mixture of stereoisomers
  • these isomers may be separated by conventional techniques such as preparative chromatography.
  • the compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution.
  • the compounds may, for example, be resolved into their components enantiomers by standard techniques, such as the formation of diastereomeric pairs by salt formation with an optically active acid, such as (-)-di-p-toluoyl-d-tartaric acid and/or (+)-di-p-toluoyl-l-tartaric acid followed by fractional crystallization and regeneration of the free base.
  • the compounds may also resolved by formation of diastereomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary. Alternatively, the compounds may be resolved using a chiral HPLC column.
  • the pharmaceutically acceptable salt generally takes a form in which an amino acids basic side chain is protonated with an inorganic or organic acid.
  • organic or inorganic acids include hydrochloric, hydrobromic, perchloric, sulfuric, nitric, phosphoric, acetic, propionic, glycolic, lactic, succinic, maleic, fumaric, malic, tartaric, citric, benzoic, mandelic, methanesulfonic, hydroxyethanesulfonic, benzenesulfonic, oxalic, pamoic, 2-naphthalenesulfonic, p-toulenesulfonic, cyclohexanesulfamic, salicylic, saccharinic or trifluoroacetic acid. All pharmaceutically acceptable acid addition salt forms of the compounds of the present invention are intended to be embraced by the scope of this invention.
  • some of the crystalline forms of the compounds may exist as polymorphs and as such are intended to be included in the present invention.
  • some of the compounds may form solvates with water (i.e. hydrates) or common organic solvents, and such solvates are also intended to be encompassed within the scope of this invention.
  • the compounds, including their salts, can also be obtained in the form of their hydrates, or include other solvents used for their crystallization.
  • the present invention further includes within its scope prodrugs of the compounds of this invention.
  • prodrugs will be functional derivatives of the compounds which are readily convertible in vivo into the desired therapeutically active compound.
  • the term “administering” shall encompass the treatment of the various disorders described with prodrug versions of one or more of the claimed compounds, but which converts to the above specified compound in vivo after administration to the subject.
  • Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in "Design of Prodrugs", ed. H. Bundgaard, Elsevier, 1985 and the patent applications DE 198 28 113, DE 198 28 114, WO 99/67228 and WO 99/67279 which are fully incorporated herein by reference.
  • Protective Groups During any of the processes for preparation of the compounds of the present invention, it may be necessary and/or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W. McOmie, Plenum Press, 1973; and T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991 , fully incorporated herein by reference. The protecting groups may be removed at a convenient subsequent stage using methods known from the art.
  • composition is intended to encompass a product comprising the claimed compounds in the therapeutically effective amounts, as well as any product which results, directly or indirectly, from combinations of the claimed compounds.
  • suitable carriers and additives may advantageously include water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents and the like;
  • suitable carriers and additives include starches, sugars, diluents, granulating agents, lubricants, binders, disintegrating agents and the like.
  • Carriers which can be added to the mixture, include necessary and inert pharmaceutical excipients, including, but not limited to, suitable binders, suspending agents, lubricants, flavorants, sweeteners, preservatives, coatings, disintegrating agents, dyes and coloring agents.
  • Soluble polymers as targetable drug carriers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamidephenol, polyhydroxyethylaspartamide- phenol, or polyethyleneoxidepolyllysine substituted with palmitoyl residue.
  • the compounds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polyactic acid, polyepsilon caprolactone, polyhydroxy butyeric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and cross-linked or amphipathic block copolymers of hydrogels.
  • Suitable binders include, without limitation, starch, gelatin, natural sugars such as glucose or betalactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth or sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride and the like.
  • Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum and the like.
  • the present invention provides compounds that act as inhibitors of glutaminyi cyclase (QC, EC 2.3.2.5). Those compounds are represented by the general formulae 1 to 6.
  • Physiological substrates of QC in mammals are, e.g. [Glu 3 ] amyloid ⁇ -protein (3-40/42), [Gin 3 ] amyloid ⁇ -protein (3-40/42), Gastrin, Neurotensin, FPP, CCL 2, CCL 7, CCL 8, CCL 16, CCL 18, Fractalkine, Orexin A, [Gln 3 ]-glucagon(3-29) and [Gln 5 ]-substance P(5-11).
  • the compounds according to the present invention and pharmaceutical compositions comprising at least one compound according to the present invention are useful for the treatment of conditions that can be treated by modulation of QC activity.
  • neuronal disorders Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
  • neuronal disorders Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
  • a QC inhibitor according to the present invention can lead to suppression of male fertility.
  • the present invention provides the use of inhibitors of QC/EC activity in combination with other agents, especially for the treatment of neuronal disorders. Detailed description of the invention
  • the present invention provides compounds having the general formula 1 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
  • n is 1 , 2, 3 or 4, preferably 2 or 3, especially 2, and A can be a saturated or unsaturated heterocycle and may be substituted or unsubstituted
  • Ri is H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri optionally being substituted independently of each other.
  • the present invention relates to compounds which can be described generally by the general formula 2 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
  • Ri, R 2 and R 3 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R and R 3 optionally being substituted independently of each other.
  • the present invention relates to compounds which can be described generally by the general formula 3 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
  • Ri and R 2 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri and R 2 optionally being substituted independently of each other.
  • the present invention relates to compounds which can be described generally by the general formula 4 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
  • n 1, 2, 3 or 4, preferably 2 or 3, especially 2, and A can be a saturated or unsaturated heterocycle and may be substituted or unsubstituted
  • Ri, R 2 and R 3 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R 2 and R 3 optionally being substituted independently of each other.
  • the present invention relates to compounds which can be described generally by the general formula 5 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
  • Ri, R 2 , R 3 , R and R 5 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R 2 , R 3> 4 and R optionally being substituted independently of each other.
  • the present invention relates to compounds which can be described generally by the general formula 6 or the pharmaceutically acceptable salts thereof, including all stereoisomers:
  • Ri, R 2 , R 3 , R4 and R 5 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R 2 , 3 , R 4 and R 5 optionally being substituted independently of each other.
  • A is a branched or unbranched C C 7 alkyl chain, a branched or unbranched C ⁇ -C 7 alkenyl chain, a branched or unbranched C ⁇ -C 7 alkynyl chain,
  • A is a compound selected from the group consisting of :
  • R 6 -R 10 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle , preferably H or methyl,
  • n and n 1 are independently 1 - 5, m is 1 - 5 , o is 0 - 4,
  • D and E are a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle,
  • D and E are a substituted phenyl, wherein substitution means oxyalkyl, thioalkyl, halogenyl, or carboxylic acid alkyl ester or aryl ester.
  • D and E are a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine.
  • Z is N.
  • X is S.
  • R 11 -R 14 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, halogenyl, oxyalkyl, thioalkyl, carboxyl, carboxylic acid ester, carbonyl, carbamide, carbimide, thiocarbamide or thiocarbonyl.
  • R 11 and R 14 are H.
  • R 12 and R 13 are independently oxyalkyl or thioalkyl, halogenyl, or carboxylic acid alkyl ester or phenyl, or R 12 and R 13 are connected to form a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine,
  • R 15 and R 16 are independently H or a branched or unbranched alkyl chain, or a branched or unbranched alkenyl chain.
  • At least one of R 15 and R 6 is H. Most preferably, R 15 and R 16 are both H.
  • R 17 and R 18 are independently of each other H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl or can be connected to form a carbocycle with up to 6 ring atoms.
  • one of R 17 and R 18 is H and the other is Me.
  • R 17 and R 18 may form a carbocycle with up to 6 ring atoms.
  • n 0 or 1
  • A is a branched or unbranched C ⁇ -C 7 alkyl chain, a branched or unbranched C C alkenyl chain, a branched or unbranched C ⁇ -C 7 alkynyl chain,
  • A is a compound selected from the group consisting of :
  • R 6 -R 10 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle , preferably H or methyl,
  • n and n 1 are independently 1 - 5, m is 1 - 5 , o is 0 - 4,
  • B is a compound selected from the group consisting of (VI) (VII)
  • D and E are a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle,
  • D and E are a substituted phenyl, wherein substitution means oxyalkyl, thioalkyl, halogenyl, carboxylic acid alkyl ester or aryl ester.
  • D and E are a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine.
  • Z is N.
  • X 1 , X and X 3 are independently O or S with the proviso for compound (XIV) that at least one of X 2 and X 3 must be S, In a preferred embodiment, X is S.
  • R 1 -R 14 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, halogenyl, oxyalkyl, thioalkyl, carboxyl, carboxylic acid ester, carbonyl, carbamide, carbimide, thiocarbamide or thiocarbonyl.
  • R 11 and R 14 are H.
  • R 12 and R 13 are independently oxyalkyl or thioalkyl, halogenyl, or carboxylic acid alkyl ester or phenyl, or R 12 and R 13 are connected to form a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine,
  • R 15 and R 16 are independently H or a branched or unbranched alkyl chain, or a branched or unbranched alkenyl chain.
  • one of R 15 and R 16 is H. Most preferably, R 15 and R 16 are both H.
  • R 17 and R 18 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl or can be connected to form a carbocycle with up to 6 ring atoms.
  • one of R 17 and R 18 is H and the other is Me.
  • R 17 and R 18 may form a carbocycle with up to 6 ring atoms.
  • n 0 or 1
  • Physiological substrates of QC in mammals are, e.g. A ⁇ 3-40/42, [Gln 3 ]A ⁇ 3-40/42, [Glu 11 ]A ⁇ 11-40/42, [Gin 11 ]A ⁇ 11-40/42, [Gln 1 ]Gastrins (17 and 34), [Gln 1 ]Neurotensin, [Gln 1 ]FPP, [Gln 1 ]TRH, [Gln 1 ]GnRH, [Gln 1 ]CCL 2, [Gln 1 ]CCL 7, [Gln 1 ]CCL 8, [Gln 1 ]CCL 16, [Gln 1 ]CCL 18, [Gln 1 ]ELA, [Gln 1 ]Fractalkine, [Gln 1 ]Orexin A, [Gln 3 ]-glucagon(3-29) and [Gln 5 ]-substance P(5-11).
  • Transepithelial transducing cells particularly the gastrin (G) cell, co-ordinate gastric acid secretion with the arrival of food in the stomach.
  • G gastrin
  • Biosynthetic precursors and intermediates are putative growth factors; their products, the amidated gastrins, regulate epithelial cell proliferation, the differentiation of acid-producing parietal cells and histamine-secreting enterochromaffin-like (ECL) cells, and the expression of genes associated with histamine synthesis and storage in ECL cells, as well as acutely stimulating acid secretion.
  • Gastrin also stimulates the production of members of the epidermal growth factor (EGF) family, which in turn inhibit parietal cell function but stimulate the growth of surface epithelial cells.
  • EGF epidermal growth factor
  • Plasma gastrin concentrations are elevated in subjects with Helicobacter pylori, who are known to have increased risk of duodenal ulcer disease and gastric cancer (Dockray, G.J. 1999 J Physiol 15315-324).
  • the peptide hormone gastrin released from antral G cells, is known to stimulate the synthesis and release of histamine from ECL cells in the oxyntic mucosa via CCK-2 receptors.
  • the mobilized histamine induces acid secretion by binding to the H(2) receptors located on parietal cells.
  • gastrin in both its fully amidated and less processed forms (progastrin and glycine-extended gastrin), is also a growth factor for the gastrointestinal tract. It has been established that the major trophic effect of amidated gastrin is for the oxyntic mucosa of stomach, where it causes increased proliferation of gastric stem cells and ECL cells, resulting in increased parietal and ECL cell mass.
  • the major trophic target of the less processed gastrin e.g. glycine-extended gastrin
  • the colonic mucosa Koh, T.J. and Chen, D. 2000 Regul Pept 9337-44.
  • Neurotensin is a neuropeptide implicated in the pathophysiology of schizophrenia that specifically modulates neurotransmitter systems previously demonstrated to be misregulated in this disorder.
  • Clinical studies in which cerebrospinal fluid (CSF) NT concentrations have been measured revealed a subset of schizophrenic patients with decreased CSF NT concentrations that are restored by effective antipsychotic drug treatment.
  • CSF cerebrospinal fluid
  • Considerable evidence also exists concordant with the involvement of NT systems in the mechanism of action of antipsychotic drugs.
  • the behavioral and biochemical effects of centrally administered NT remarkably resemble those of systemically administered antipsychotic drugs, and antipsychotic drugs increase NT neurotransmission. This concatenation of findings led to the hypothesis that NT functions as an endogenous antipsychotic.
  • FPP Fertilization promoting peptide
  • TRH thyrotrophin releasing hormone
  • FPP and adenosine have been shown to stimulate cAMP production in uncapacitated cells but inhibit it in capacitated cells, with FPP receptors somehow interacting with adenosine receptors and G proteins to achieve regulation of AC. These events affect the tyrosine phosphorylation state of various proteins, some being important in the initial "switching on,” others possibly being involved in the acrosome reaction itself.
  • Calcitonin and angiotensin II also found in seminal plasma, have similar effects in vitro on uncapacitated spermatozoa and can augment responses to FPP. These molecules have similar effects in vivo, affecting fertility by stimulating and then maintaining fertilizing potential.
  • CCL2, CCL7, CCL8, CCL16, CCL18 and fractalkine play an important role in pathophysiological conditions, such as suppression of proliferation of myeloid progenitor cells, neoplasia, inflammatory host responses, cancer, psoriasis, rheumatoid arthritis, atherosclerosis, humoral and cell-mediated immunity responses, leukocyte adhesion and migration processes at the endothelium.
  • cytotoxic T lymphocyte peptide-based vaccines against hepatitis B, human immunodeficiency virus and melanoma were recently studied in clinical trials.
  • This peptide is a Melan-A/MART-1 antigen immunodominant peptide analog, with an N-terminal glutamic acid. It has been reported that the amino group and gamma-carboxylic group of glutamic acids, as well as the amino group and gamma-carboxamide group of glutamines, condense easily to form pyroglutamic derivatives.
  • Orexin A is a neuropeptide that plays a significant role in the regulation of food intake and sleep-wakefulness, possibly by coordinating the complex behavioral and physiologic responses of these complementary homeostatic functions. It plays also a role in the homeostatic regulation of energy metabolism, autonomic function, hormonal balance and the regulation of body fluids.
  • the present invention provides imidazole and its derivatives and histidine and its derivatives as activity reducing effectors of QC and their characteristics in terms of inhibition type and potency. Structures and K,-values are shown in tables 2 and 3. The results are described in detail in example 2.
  • Table 2 Inhibitory constants of imidazole derivatives in the human QC catalyzed reaction. Determinations were performed at 30 °C in 0.05 M Tris-HCI pH 8.0, containing 5 mM EDTA.
  • N-terminal glutaminyi residue besides a N-terminal glutaminyi residue, also N-terminal ⁇ -homo- glutaminyl residues fulfill properties as substrate of QCs from plants and mammals.
  • the N-terminal ⁇ -homo-glutaminyl residue was converted into a five-membered lactam ring by catalysis of human and papaya QC, respectively.
  • Another preferred embodiment of the present invention comprises screening methods for inhibitors of QC.
  • a preferred screening method for identifying QC inhibitors from a group of compounds comprises the steps of: a) Contacting said compounds with QC under conditions which would permit binding therebetween; b) Adding a substrate of QC; c) Monitoring the conversion of the substrate or optionally measuring the residual QC activity; and d) Calculating changes in the substrate conversion and/or enzyme activity of QC to identify an activity modifying effector.
  • Another preferred screening method relates to a method for the identification and selection of inhibitors which interact directly or indirectly with the active-site bound metal ion of QC and comprises the following steps: a) Contacting said compounds with QC under conditions which would permit binding therebetween; b) Adding a substrate of QC which is subject to conversion by QC; c) Monitoring the conversion of the substrate or optionally measuring the residual QC activity; and d) Calculating changes in the substrate conversion and/or enzyme activity of QC wherein changes may be used to identify an activity modifying effector of QC.
  • mammalian QC or Papaya QC.
  • mammalian QC since the inhibitors identified by these screening methods shall be used for the treatment of diseases in mammals, especially in humans.
  • a QC-inhibitor and/or a combination according to the present invention By administering a QC-inhibitor and/or a combination according to the present invention to a mammal it can be possible to prevent or alleviate or treat conditions selected from Alzheimer's disease, Down Syndrome, ulcer disease and gastric cancer with or w/o Helicobacter pylori infections, neoplasia, inflammatory host responses, cancer, melanoma, malign metastasis, psoriasis, rheumatoid arthritis, atherosclerosis, leukocyte adhesion and migration processes in the endothelium, impaired food intake, sleep- wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance and impaired regulation of body fluids.
  • a QC-inhibitor and/or a combination according to the present invention can be administered to a mammal it can be possible to stimulate the proliferation of myeloid progenitor cells.
  • a QC-inhibitor and/or a combination according to the present invention can lead to suppression of male fertility.
  • the present invention provides the use of inhibitors of QC/EC activity in combination with inhibitors of DP IV or DP IV-like enzymes for the treatment or alleviation of conditions that can be treated by modulation of QC and/or DP IV activity.
  • the present invention provides the use of inhibitors of QC/EC activity in combination with inhibitors of PEP for the treatment or alleviation of conditions that can be treated by modulation of QC/EC and/or PEP activity.
  • NPY-receptor-ligands NPY agonists and/or NPY antagonists.
  • ACE acetylcholinesterase
  • the present invention provides pharmaceutical compositions for parenteral, enteral or oral administration, comprising at least one inhibitor of QC (EC) optionally in combination with customary carriers and/or excipients; or comprising at least one inhibitor of QC (EC) in combination with at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor-ligand, optionally in combination with customary carriers and/or excipients.
  • at least one inhibitor of QC EC
  • PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor-ligand optionally in combination with customary carriers and/or excipients.
  • neuronal disorders Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
  • neuronal disorders Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
  • the invention provides a method for the treatment of neuronal disorders (Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep- wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
  • neuronal disorders Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep- wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
  • the method comprises either co-administration of a QC-inhibitor and/or at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor- ligand and/or at least one ACE-inhibitor or the sequential administration thereof.
  • Co-administration includes administration of a formulation which includes at least one QC-inhibitor and/or at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor-ligand and/or at least one ACE-inhibitor or the essentially simultaneous administration of separate formulations of each agent.
  • the invention provides the use of at least one QC-inhibitor and/or at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY- receptor-ligand and/or at least one ACE-inhibitor for use in the manufacture of a composition for the treatment of neuronal disorders.
  • the present invention provides pharmaceutical compositions for parenteral, enteral or oral administration, comprising at least one inhibitor of QC (EC) optionally in combination with customary carriers and/or excipients; or comprising at least one inhibitor of QC in combination with at least one DP IV-inhibitor, optionally in combination with customary carriers and/or excipients.
  • Suitable inhibitors of prolyl endopeptidase are, e.g. chemical derivatives of proline or small peptides containing terminal prolines.
  • Benzyloxycarbonyl-prolyl-prolinal has been shown to be a specific transition state inhibitor of the enzyme (Wilk, S. and Orloeski, M., J. Neurochem., 41 , 69 (1983), Friedman, et al., Neurochem., 42, 237 (1984)).
  • N- terminal substitutions of L-proline or L-prolylpyrrolidine (Atack, et al., Eur. J.
  • EP-A-0 286 928 discloses 2-acylpyrrolidine derivatives useful as propyl endopeptidase inhibitors.
  • Further suitable prolyl endopeptidase inhibitors according to the present invention are, e.g. Fmoc-Ala-Pyrr-CN and those listed below:
  • prolyl endopeptidase inhibitors are disclosed in JP 01042465, JP 03031298, JP 04208299, WO 0071144, US 5847155; JP 09040693, JP 10077300, JP 05331072, JP 05015314, WO 9515310, WO 9300361 , EP 0556482, JP 06234693, JP 01068396, EP 0709373, US 5965556, US 5756763, US 6121311 , JP 63264454, JP 64000069, JP 63162672, EP 0268190, EP 0277588, EP 0275482, US 4977180, US 5091406, US 4983624, US 5112847, US 5100904, US 5254550, US 5262431 , US 5340832, US 4956380, EP 0303434, JP 03056486, JP 01143897, JP 1226880, EP 0280956, US
  • Suitable DP IV-inhibitors are are agents such as tetrahydroisoquinolin-3-carboxamide derivatives, N-substituted 2-cyanopyroles and -pyrrolidines, N-(N'-substituted glycyl)-2- cyanopyrrolidines, N-(substituted glycyl)-thiazolidines, N-(substituted glycyl)-4- cyanothiazolidines, boronyl inhibitors and cyclopropyl-fused pyrrolidines.
  • Inhibitors of dipeptidyl peptidase IV are described in US 6,011 ,155; US 6,107,317; US 6,110,949; US 6,124,305; US 6,172,081; WO 99/61431, WO 99/67278, WO 99/67279, DE 198 34 591 , WO 97/40832, DE 196 16 486 C 2, WO 95/15309, WO 98/19998, WO 00/07617, WO 99/38501 , WO 99/46272, WO 99/38501 , WO 01/68603, WO 01/40180, WO 01/81337, WO 01/81304, WO 01/55105, WO 02/02560, WO 01/34594, WO 02/38541 (Japanese), WO 02/ 083128, WO 03/072556, WO 03/002593, WO 03/000250, WO 03/000180, WO 03/000181 , EP 1
  • Preferred DP IV-inhibitors include valine pyrrolidide (Novo Nordisk), NVP-DPP728A (1-[ [ [ 2-[ ⁇ 5-cyanopyridin-2-yl ⁇ amino]ethyl]amino]acetyl]-2-cyano-(S)-pyrrolidine) (Novartis) as disclosed by Hughes et al., Biochemistry, 38 (36), 11597-11603, 1999, LAF-237 (1- [(3-hydroxy-adamant-1-ylamino)-acetyl]-pyrrolidine-2(S)-carbonitrile); disclosed by Hughes et al., Meeting of the American Diabetes Association 2002, Abstract no.
  • TSL-225 tryptophyl-1 ,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
  • Yamada et. al. Bioorg. & Med. Chem. Lett. 8 (1998), 1537-1540, 2- cyanopyrr ⁇ lidides and 4-cyanopyrrolidides as disclosed by Asworth et al., Bioorg. & Med. Chem. Lett., 6, No.
  • NPY neuropeptide Y
  • NPY mimetic NPY mimetic
  • NPY agonist or antagonist NPY ligand of the NPY receptors.
  • Preferred according to the present invention are antagonists of the NPY receptors.
  • Suitable ligands or antagonists of the NPY receptors are 3a,4,5,9b-tetrahydro-1h- benz[e]indol-2-yl amine-derived compounds as disclosed in WO 00/68197.
  • NPY receptor antagonists which may be mentioned include those disclosed in European patent applications EP 0 614 911 , EP 0 747 357, EP 0 747 356 and EP 0 747 378; international patent applications WO 94/17035, WO 97/19911 , WO 97/19913, WO 96/12489, WO 97/19914, WO 96/22305, WO 96/40660, WO 96/12490, WO 97/09308, WO 97/20820, WO 97/20821 , WO 97/20822, WO 97/20823, WO 97/19682, WO 97/25041 , WO 97/34843, WO 97/46250, WO 98/03492, WO 98/03493, WO 98/03494 and WO 98/07420; WO 00/30674, US patents Nos.
  • NPY antagonists include those compounds that are specifically disclosed in these patent documents. More preferred compounds include amino acid and non-peptide-based NPY antagonists.
  • Amino acid and non-peptide-based NPY antagonists which may be mentioned include those disclosed in European patent applications EP 0 614 911 , EP 0 747 357, EP 0 747 356 and EP 0 747 378; international patent applications WO 94/17035, WO 97/19911 , WO 97/19913, WO 96/12489, WO 97/19914, WO 96/22305, WO 96/40660, WO 96/12490, WO 97/09308, WO 97/20820, WO 97/20821 , WO 97/20822, WO 97/20823, WO 97/19682, WO 97/25041 , WO 97/34843, WO 97/46250, WO 98/03492, WO 98/03493, WO 98/03494, WO 98/07420 and WO 99/15498 ; US patents Nos. 5,552,411 ,5,
  • Particularly preferred compounds include amino acid-based NPY antagonists.
  • Amino acid-based compounds which may be mentioned include those disclosed in international patent applications WO 94/17035, WO 97/19911 , WO 97/19913, WO 97/19914 or, preferably, WO 99/15498.
  • Preferred amino acid-based NPY antagonists include those that are specifically disclosed in these patent documents, for example BIBP3226 and, especially, (R)-N2-(diphenylacetyl)-(R)-N-[1-(4-hydroxy- phenyl) ethyl] arginine amide (Example 4 of international patent application WO 99/15498).
  • Preferred DP IV-inhibitors are dipeptide-like compounds and compounds analogous to dipeptide compounds that are formed from an amino acid and a thiazolidine or pyrrolidine group, and salts thereof, referred to hereinafter as dipeptide-like compounds.
  • the amino acid and the thiazolidine or pyrrolidine group are bonded with an amide bond.
  • Such compounds are disclosed in WO 99/61431.
  • dipeptide-like compounds in which the amino acid is preferably selected from a natural amino acid, such as, for example, leucine, valine, glutamine, glutamic acid, proline, isoleucine, asparagines and aspartic acid.
  • a natural amino acid such as, for example, leucine, valine, glutamine, glutamic acid, proline, isoleucine, asparagines and aspartic acid.
  • the dipeptide-like compounds used according to the invention exhibit at a concentration (of dipeptide compounds) of 10 ⁇ M, a reduction in the activity of plasma dipeptidyl peptidase IV or DP IV-analogous enzyme activities of at least 10 %, especially of at least 40 %. Frequently a reduction in activity of at least 60 % or at least 70 % is also required. Preferred agents may also exhibit a reduction in activity of a maximum of 20 % or 30 %.
  • Preferred compounds are N-valyl prolyl, O-benzoyl hydroxy la mine, alanyl pyrrolidine, isoleucyl thiazolidine like L-allo-isoleucyl thiazolidine, L-threo-isoleucyl pyrrolidine and salts thereof, especially the fumaric salts, and L-allo-isoleucyl pyrrolidine and salts thereof.
  • Especially preferred compounds are glutaminyi pyrrolidine and glutaminyi thiazolidine of formulas 8 and 9:
  • the salts of the dipeptide-like compounds can be present in a molar ratio of dipeptide (- analogous) component to salt component of 1 : 1 or 2 : 1.
  • a salt is, for example, (lle-Thia) 2 fumaric acid.
  • Table 4 Structures of further preferred dipeptide compounds
  • Peptide structures as disclosed in WO 03/002593 e.g. f-butyl-Gly-Pro-D-Val, t- butyl-Gly -Pro-Gly, f-butyl-Gly -Pro-lie, f-butyl-Gly -Pro-lie-amide, f-butyl-Gly-Pro- f-butyl-Gly, f-butyl-Gly-Pro-Val,
  • Substituted aminoketone compounds as disclosed in WO 03/040174 e.g. 1- cyclopentyl-3-methyl-1-oxo-2-pentanaminium chloride, 7-cyclopentyl-3-methyl-1 - oxo-2-butanaminium chloride, 1-cyclopentyl-3,3-dimethyl-1-oxo-2-butanaminium chloride, 1-cyclohexyl-3,3-dimethyl-1-oxo-2-butanaminium chloride, 3- (cyclopentylcarbonyl)-1 ,2,3,4-tetrahydroisoquinolinium chloride, and N-(2- cyclopentyl-2-oxoethyl)cyclohexanaminium chloride,
  • At least one effector of QC optionally in combination with at least one PEP-inhibitor and/or at least one DP IV- inhibitor and/or at least one NPY-receptor-ligand and/or at least one ACE-inhibitor, can be used as the active ingredient(s).
  • the active ingredient(s) is intimately admixed with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques, which carrier may take a wide variety of forms depending of the form of preparation desired for administration, e.g., oral or parenteral such as intramuscular.
  • any of the usual pharmaceutical media may be employed.
  • suitable carriers and additives include water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents and the like;
  • suitable carriers and additives include starches, sugars, diluents, granulating agents, lubricants, binders, disintegrating agents and the like. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit form, in which case solid pharmaceutical carriers are obviously employed. If desired, tablets may be sugar coated or enteric coated by standard techniques.
  • the carrier will usually comprise sterile water, through other ingredients, for example, for purposes such as aiding solubility or for preservation, may be included.
  • Injectable suspensions may also prepared, in which case appropriate liquid carriers, suspending agents and the like may be employed.
  • the pharmaceutical compositions herein will contain, per dosage unit, e.g., tablet, capsule, powder, injection, teaspoonful and the like, an amount of the active ingredient(s) necessary to deliver an effective dose as described above.
  • the pharmaceutical compositions herein will contain, per dosage unit, e.g., tablet, capsule, powder, injection, suppository, teaspoonful and the like, from about 0.03 mg to 100 mg/kg (preferred 0.1 - 30 mg/kg) and may be given at a dosage of from about 0.1 - 300 mg/kg per day (preferred 1 - 50 mg/kg per day) of each active ingredient or combination thereof.
  • the dosages may be varied depending upon the requirement of the patients, the severity of the condition being treated and the compound being employed. The use of either daily administration or post-periodic dosing may be employed.
  • compositions are in unit dosage forms from such as tablets, pills, capsules, powders, granules, sterile parenteral solutions or suspensions, metered aerosol or liquid sprays, drops, ampoules, autoinjector devices or suppositories; for oral parenteral, intranasal, sublingual or rectal administration, or for administration by inhalation or insufflation.
  • the composition may be presented in a form suitable for once-weekly or once-monthly administration; for example, an insoluble salt of the active compound, such as the decanoate salt, may be adapted to provide a depot preparation for intramuscular injection.
  • a pharmaceutical carrier e.g.
  • a solid preformulation composition containing a homogeneous mixture of a compound of the present invention, or a pharmaceutically acceptable salt thereof.
  • preformulation compositions as homogeneous, it is meant that the active ingredient is dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective dosage forms such as tablets, pills and capsules. This solid preformulation composftion is then subdivided into unit dosage forms of the type described above containing from 0.1 to about 500 mg of each active ingredient or combinations thereof of the present invention.
  • the tablets or pills of the compositions of the present invention can be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action.
  • the tablet or pill can comprise an inner dosage and an outer dosage component, the latter being in the form of an envelope over the former.
  • the two components can be separated by an enteric layer which serves to resist disintegration in the stomach and permits the inner component to pass intact into the duodenum or to be delayed in release.
  • enteric layers or coatings such materials including a number of polymeric acids with such materials as shellac, cetyl alcohol and cellulose acetate.
  • Suitable dispersing or suspending agents for aqueous suspensions include synthetic and natural gums such as tragacanth, acacia, alginate, dextran, sodium carboxymethylcellulose, methylcellulose, polyvinylpyrrolidone or gelatin.
  • the processes for the preparation of the compounds of the present invention give rise to mixture of stereoisomers
  • these isomers may be separated by conventional techniques such as preparative chromatography.
  • the compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution.
  • the compounds may, for example, be resolved into their components enantiomers by standard techniques, such as the formation of diastereomeric pairs by salt formation with an optically active acid, such as (-)-di-p- toluoyl-d-tartaric acid and/or (+)-di-p-toluoyl-!-tartaric acid followed by fractional crystallization and regeneration of the free base.
  • the compounds may also resolved by formation of diastereomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary. Alternatively, the compounds may be resolved using a chiral HPLC column.
  • any of the processes for preparation of the compounds of the present invention it may be necessary and/or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W. McOmie, Plenum Press, 1973; and T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991.
  • the protecting groups may be removed at a convenient subsequent stage using conventional methods known from the art.
  • the method of treating neuronal disorders as described in the present invention may also be carried out using a pharmaceutical composition at least one effector of QC optionally in combination with at least one PEP-inhibitor and/or at least one DP IV- inhibitor and/or at least one NPY-receptor-ligand and/or at least one ACE-inhibitor or any other of the compounds as defined herein and a pharmaceutically acceptable carrier.
  • the pharmaceutical composition may contain between about 0.01 mg and 100 mg, preferably about 5 to 50 mg, of each compound, and may be constituted into any form suitable for the mode of administration selected.
  • Carriers include necessary and inert pharmaceutical excipients, including, but not limited to, binders, suspending agents, lubricants, flavorants, sweeteners, preservatives, dyes, and coatings.
  • Compositions suitable for oral administration include solid forms, such as pills, tablets, caplets, capsules (each including immediate release, timed release and sustained release formulations), granules, and powders, and liquid forms, such as solutions, syrups, elixirs, emulsions, and suspensions.
  • Forms useful for parenteral administration include sterile solutions, emulsions and suspensions.
  • compounds of the present invention may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three or four times daily.
  • compounds for the present invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal skin patches well known to those of ordinary skill in that art.
  • the dosage administration will, of course, be continuous rather than intermittent throughout the dosage regimen.
  • the active drug component can be combined with an oral, non-toxic pharmaceutically acceptable inert carrier such as ethanol, glycerol, water and the like.
  • suitable binders include, without limitation, starch, gelatin, natural sugars such as glucose or betalactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth or sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride and the like.
  • Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum and the like.
  • liquid forms in suitable flavored suspending or dispersing agents such as the synthetic and natural gums, for example, tragacanth, acacia, methyl-cellulose and the like.
  • suitable suspending or dispersing agents such as the synthetic and natural gums, for example, tragacanth, acacia, methyl-cellulose and the like.
  • tragacanth for example, tragacanth, acacia, methyl-cellulose and the like.
  • methyl-cellulose methyl-cellulose and the like.
  • suitable suspending or dispersing agents such as the synthetic and natural gums, for example, tragacanth, acacia, methyl-cellulose and the like.
  • sterile suspensions and solutions are desired.
  • Isotonic preparations which generally contain suitable preservatives are employed when intravenous administration is desired.
  • the compounds or combinations of the present invention can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles.
  • Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine or phosphatidylcholines.
  • Compounds or combinations of the present invention may also be delivered by the use of monoclonal antibodies as individual carriers to which the compound molecules are coupled.
  • the compounds of the present invention may also be coupled with soluble polymers as targetable drug carriers.
  • Such polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamidephenol, polyhydroxyethylaspartamid-ephenol, or polyethyl eneoxidepolyllysine substituted with palmitoyl residue.
  • the compounds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polyactic acid, polyepsilon caprolactone, polyhydroxy butyeric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and cross-linked or amphipathic block copolymers of hydrogels.
  • biodegradable polymers useful in achieving controlled release of a drug, for example, polyactic acid, polyepsilon caprolactone, polyhydroxy butyeric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and cross-linked or amphipathic block copolymers of hydrogels.
  • Compounds or combinations of this invention may be administered in any of the foregoing compositions and according to dosage regimens established in the art whenever treatment of the addressed disorders is required.
  • the daily dosage of the products may be varied over a wide range from 0.01 to 1.000 mg per mammal per day.
  • the compositions are preferably provided in the form of tablets containing, 0.01 , 0.05, 0.1 , 0.5, 1.0, 2.5, 5.0, 10.0, 15.0, 25.0, 50.0, 100, 150, 200, 250 and 500 milligrams of each active ingredient or combinations thereof for the symptomatic adjustment of the dosage to the patient to be treated.
  • An effective amount of the drug is ordinarily supplied at a dosage level of from about 0.1 mg/kg to about 300 mg/kg of body weight per day.
  • the range is from about 1 to about 50 mg/kg of body weight per day.
  • the compounds or combinations may be administered on a regimen of 1 to 4 times per day.
  • Optimal dosages to be administered may be readily determined by those skilled in the art, and will vary with the particular compound used, the mode of administration, the strength of the preparation, the mode of administration, and the advancement of disease condition. In addition, factors associated with the particular patient being treated, including patient age, weight, diet and time of administration, will result in the need to adjust dosages.
  • the particularly beneficial effect provided by the treatment of the invention is an improved therapeutic ratio for the combination of the invention relative to the therapeutic ratio for one compound of the combination when used alone and at a dose providing an equivalent efficacy to the combination of the invention.
  • the particularly beneficial effect provided by the treatment of the invention is indicated to be a synergistic effect relative to the control expected from the effects of the individual active agents.
  • combining doses of at least one QC-inhibitor with at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY- receptor-ligand will produce a greater beneficial effect than can be achieved for either agent alone at a dose twice that used for that agent in the combination.
  • the dosage level of each of the active agents when used in accordance with the treatment of the invention will be less than would have been required from a purely additive effect upon the neuronal condition.
  • the treatment of the invention will effect an improvement, relative to the individual agents, in decreasing the intracellular deposition of pGlu- amyloid- ⁇ -peptides and thereby dramatically slowing down the plaque formation in the brain of a mammal, preferably in human brain.
  • the invention also provides a process for preparing a pharmaceutical composition
  • a pharmaceutical composition comprising at least one at least one effector of QC optionally in combination with at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor-ligand and/or at least one ACE-inhibitor and a pharmaceutically acceptable carrier therefor, which process comprises admixing the QC effector and/or DP IV-inhibitor and/or the PEP-inhibitor and/or the NPY-receptor-ligand and/or the ACE- inhibitor and a pharmaceutically acceptable carrier.
  • compositions are preferably in a unit dosage form in an amount appropriate for the relevant daily dosage.
  • suitable dosages, including especially unit dosages, of the QC-inhibitor, the PEP- inhibitor, the DP IV-inhibitor and the NPY-receptor-ligand include the known dosages including unit doses for these compounds as described or referred to in reference text such as the British and US Pharmacopoeias, Remington's Pharmaceutical Sciences (Mack Publishing Co.), Martindale The Extra Pharmacopoeia (London, The Pharmaceutical Press) (for example see the 31st Edition page 341 and pages cited therein) or the above mentioned publications.
  • Synthesis scheme 1 synthesis of the examples 1-22, 36, 37
  • Reagents and conditions (a) NaH, DMF, 4h, rt.; (b) ?-?, 8h, 100°C; (c) H 2 N-NH 2l EtOH, 8h, reflux then 4N HCl, 6h, reflux, (d) R-NCO, EtOH, 6h, reflux, (e) R-NCS, 6h, reflux
  • Synthesis scheme 3 synthesis of the examples 31-35 Reagents and conditions: (a) Mel, CH 2 CI 2 , rt.,1h; (b) H 2 N-CN, BuOH, reflux, 8h
  • Synthesis scheme 4 synthesis of the examples 38-40 Reagents and conditions: (a) NaH, DMF, rt.,3h; (b) LiAIH 4 , dioxane, reflux, 1 h; (c) R-NCS, EtOH, reflux 6h,
  • the 1/-/-imidazole-1-alkylamines were prepared according to the literature from ⁇ -brom- alkyl-phtalimides and imidazolium salt and. subsequent hydrazinolysis. The resulting products were transformed into the thioureas according to example 1-21 giving a 88% (example 36) and 95% (example 37) yield.
  • Imidazole was reacted with the corresponding brommethylphenylcyanide in DMF, utilizing 1 equivalent of NaH for 3h under rt., giving the 1H-imidazole-1- methylphenylcyanides.
  • the solvent was removed and the resulting oil was redissolved in dioxane.
  • the cyanides were converted in the corresponding amines using 1 equivalent of LiAIH .
  • dioxane was evaporated and the aqueous layer was extracted by means of CHCI 3 .
  • the peptides used herein were synthesized with an automated synthesizer SYMPHONY (RAININ) using a modified Fmoc-protocol. Cycles were modified by using double couplings from the 15 th amino acid from the C-terminus of the peptide with fivefold excess of Fmoc-amino acids and coupling reagent.
  • the peptide couplings were performed by TBTU/NMM-activation using a 0.23 mmol substituted NovaSyn TGR-resin or the corresponding preloaded Wang-resin at 25 ⁇ mol scale.
  • the cleavage from the resin was carried out by a cleavage-cocktail consisting of 94.5 % TFA, 2.5 % water, 2.5 % EDT and 1 % TIS.
  • laser desorption mass spectrometry was employed using the HP G2025 MALDI-TOF system of Hewlett- Packard.
  • Example 1 Determination of IC ⁇ o-values of DP IV-inhibitors
  • DP IV activity was measured in the same way as described in example 2 at final substrate concentrations of 0.05, 0.1 , 0.2, and 0.4 mM and further 7 inhibitor concentrations covering the IC 50 concentration. Calculations were performed using the GraFit Software.
  • QC activity was determined from a standard curve of ⁇ -naphthylamine under assay conditions. One unit is defined as the amount of QC catalyzing the formation of 1 ⁇ mol pGlu-/5NA from H-Gln- ⁇ NA per minute under the described conditions.
  • QC was activity was determined using H-Gln-AMC as substrate. Reactions were carried out at 30°C utilizing the NOVOStar reader for microplates (BMG lab-technologies).
  • the samples consisted of varying concentrations of the fluorogenic substrate, 0.1 U pyroglutamyl aminopeptidase (Qiagen) in 0.05 M Tris/HCI, pH 8.0 containing 5 mM EDTA and an appropriately diluted aliquot of QC in a final volume of 250 ⁇ l. Excitation/emission wavelengths were 380/460 nm.
  • the assay reactions were initiated by addition of glutaminyi cyclase.
  • QC activity was determined from a standard curve of 7-amino-4-methylcoumarin under assay conditions. The kinetic data were evaluated using GraFit sofware.
  • This novel assay was used to determine the kinetic parameters for most of the QC substrates.
  • QC activity was analyzed spectrophotometrically using a continuous method, that was derived by adapting a previous discontinuous assay (Bateman, R. C. J. 1989 J Neurosci Methods 30, 23-28) utilizing glutamate dehydrogenase as auxiliary enzyme.
  • Samples consisted of the respective QC substrate, 0.3 mM NADH, 14 mM ⁇ - Ketoglutaric acid and 30 U/ml glutamate dehydrogenase in a final volume of 250 ⁇ l. Reactions were started by addition of QC and persued by monitoring of the decrease in absorbance at 340 nm for 8-15 min.
  • the initial velocities were evaluated and the enzymatic activity was determined from a standard curve of ammonia under assay conditions. All samples were measured at 30°C, using either the SPECTRAFIuor Plus or the Sunrise (both from TECAN) reader for microplates. Kinetic data was evaluated using GraFit software.
  • the sample composition was the same as described above, except of the putative inhibitory compound added.
  • samples contained 4 mM of the respective inhibitor and a substrate concentration at 1 KM-
  • influence of the inhibitor on the auxiliary enzymes was investigated first. In every case, there was no influence on either enzyme detected, thus enabling the reliable determination of the QC inhibition.
  • the inhibitory constant was evaluated by fitting the set of progress curves to the general equation for competitive inhibition using GraFit software.
  • N-1 derivatives N-1 derivatives.
  • imidazole derivatives tested on inhibition of human QC most compounds that had improved Kj-values compared to imidazole showed alterations at one nitrogen atom. These compounds also contained one of the most effective QC inhibitors, 1-benzylimidazole. Interestingly, only little alterations of this structure led to a loss of inhibitory quality, as can be seen for 1-benzoylimidazole and phenylimidazole, which was inactive under the experimental conditions.
  • Example 6 MALDI-TOF mass spectrometry
  • Matrix-assisted laser desorption/ionization mass spectrometry was carried out using the Hewlett-Packard G2025 LD-TOF System with a linear time of flight analyzer.
  • the instrument was equipped with a 337 nm nitrogen laser, a potential acceleration source (5 kV) and a 1.0 m flight tube.
  • Detector operation was in the positive-ion mode and signals were recorded and filtered using LeCroy 9350M digital storage oscilloscope linked to a personal computer. Samples (5 ⁇ l) were mixed with equal volumes of the matrix solution.
  • DHAP/DAHC prepared by solving 30 mg 2 ' ,6 ' -dihydroxyacetophenone (Aldrich) and 44 mg diammonium hydrogen citrate (Fluka) in 1 ml acetonitrile/0.1% TFA in water (1/1 , v/v). A small volume ( « 1 ⁇ l) of the matrix-analyte-mixture was transferred to a probe tip and immediately evaporated in a vacuum chamber (Hewlett-Packard G2024A sample prep accessory) to ensure rapid and homogeneous sample crystallization.
  • a ⁇ -derived peptides were incubated in 100 ⁇ l 0.1 M sodium acetate buffer, pH 5.2 or 0.1 M Bis-Tris buffer, pH 6.5 at 30°C. Peptides were applied in 0.5 mM [A ⁇ (3-11)a] or 0.15 mM [A ⁇ (3-21)a] concentrations, and 0.2 U QC was added all 24 hours.
  • the assays contained 1 % DMSO.
  • samples were removed from the assay tube, peptides extracted using ZipTips (Millipore) according to the manufacturer ' s recommendations, mixed with matrix solution (1 :1 v/v) and subsequently the mass spectra recorded. Negative controls did either contain no QC or heat deactivated enzyme.
  • the sample composition was the same as described above, with exception of the inhibitory compound added (5 mM benzimidazole or 2 mM 1 ,10-phenanthroline).

Abstract

The present invention relates to compounds that act as inhibitors of QC including those represented by the general formulae ( 1 to 9): and combinations thereof for the treatment of neuronal disorders, especially Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleepwakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia.

Description

Inhibitors of Glutaminyi Cyclase
Field of the invention
The invention relates to glutaminyi cyclase (QC, EC 2.3.2.5) that catalyzes the intramolecular cyclization of N-terminal glutamine residues into pyroglutamic acid (5- oxo-prolyl, pGlu*) under liberation of ammonia and the intramolecular cyclization of N- terminal glutamate residues into pyroglutamic acid under liberation of water.
Background of the invention
Glutaminyi cyclase (QC, EC 2.3.2.5) catalyzes the intramolecular cyclization of N- terminal glutamine residues into pyroglutamic acid (pGlu*) liberating ammonia. A QC was first isolated by Messer from the latex of the tropical plant Caήca papaya in 1963 (Messer, M. 1963 Nature 4874, 1299). 24 years later, a corresponding enzymatic activity was discovered in animal pituitary (Busby, W. H. J. et al. 1987 J Biol Chem 262, 8532-8536; Fischer, W. H. and Spiess, J. 1987 Proc Natl Acad Sci U S A 84, 3628- 3632). For the mammalian QC, the conversion of Gin into pGlu by QC could be shown for the precursors of TRH and GnRH (Busby, W. H. J. et al. 1987 J Biol Chem 262, 8532-8536; Fischer, W. H. and Spiess, J. 1987 Proc Natl Acad Sci U S A 84, 3628- 3632). In addition, initial localization experiments of QC revealed a co-localization with its putative products of catalysis in bovine pituitary, further improving the suggested function in peptide hormone synthesis (Bockers, T. M. et al. 1995 J Neuroendocrinol 7, 445-453). In contrast, the physiological function of the plant QC is less clear. In case of the enzyme from C. papaya, a role in the plant defense against pathogenic microorganisms was suggested (El Moussaoui, A. et al.2001 Cell Mol Life Sci 58, 556- 570). Putative QCs from other plants were identified by sequence comparisons recently (Dahl, S. W. et al.2000 Protein Expr Purif 20, 27-36) The physiological function of these enzymes, however, is still ambiguous.
The QCs known from plants and animals show a strict specificity for L-Glutamine in the N-terminal position of the substrates and their kinetic behavior was found to obey the Michaelis-Menten equation (Pohl, T. et al. 1991 Proc Natl Acad Sci U S A 88, 10059- 10063; Consalvo, A. P. et al. 1988 Anal Biochem 175, 131-138; Gololobov, M. Y. et al. 1996 Biol Chem Hoppe Seyler 377, 395-398). A comparison of the primary structures of the QCs from C. papaya and that of the highly conserved QC from mammals, however, did not reveal any sequence homology (Dahl, S. W. et al. 2000 Protein Expr Purif 20, 27-36). Whereas the plant QCs appear to belong to a new enzyme family (Dahl, S. W. et al. 2000 Protein Expr Purif 20, 27-36), the mammalian QCs were found to have a pronounced sequence homology to bacterial aminopeptidases (Bateman, R. C. et al. 2001 Biochemistry 40, 11246-11250), leading to the conclusion that the QCs from plants and animals have different evolutionary origins.
Recently, it was shown that recombinant human QC as well as QC-activity from brain extracts catalyze both, the N-terminal glutaminyi as well as glutamate cyclization. Most striking is the finding, that cyclase-catalyzed Glu1 -conversion is favored around pH 6.0 while Gin 1 -conversion to pGlu-derivatives occurs with a pH-optimum of around 8.0. Since the formation of pGlu-Aβ-related peptides can be suppressed by inhibition of recombinant human QC and QC-activity from pig pituitary extracts, the enzyme QC is a target in drug development for treatment of Alzheimer's disease.
EP 02 011 349.4 discloses polynucleotides encoding insect glutaminyi cyclase, as well as polypeptides encoded thereby. This application further provides host cells comprising expression vectors comprising polynucleotides of the invention. Isolated polypeptides and host cells comprising insect QC are useful in methods of screening for agents that reduce glutaminyi cyclase activity. Such agents are useful as pesticides.
Definitions
The term "DP IV-inhibitor" or "dipeptidyl peptidase IV inhibitor" is generally known to a person skilled in the art and means enzyme inhibitors, which inhibit the catalytical activity of DP IV or DP IV-like enzymes.
„DP IV-activity" is defined as the catalytical activity of dipeptidyl peptidase IV (DP IV) and DP IV-like enzymes. These enzymes are post-proline (to a lesser extent post- alanine, post-serine or post-glycine) cleaving serine proteases found in various tissues of the body of a mammal including kidney, liver, and intestine, where they remove dipeptides from the N-terminus of biologically active peptides with a high specificity when proline or alanine form the residues that are adjacent to the N-terminal amino acid in their sequence.
The term "PEP-inhibitor" or "prolyl endopeptidase inhibitor" is generally known to a person skilled in the art and means enzyme inhibitors, which inhibit the catalytical activity of prolyl endopeptidase (PEP).
The term "QC" as used herein comprises glutaminyi cyclase (QC) and QC-like enzymes. QC and QC-like enzymes have identical or similar enzymatic activity, further defined as QC activity. In this regard, QC-like enzymes can fundamentally differ in their molecular structure from QC.
The term "QC activity" as used herein is defined as intramolecular cyclization of N- terminal glutamine residues into pyroglutamic acid (pGlu*) or of N-terminal L- homoglutamine or L-β-homoglutamine to a cyclic pyro-homoglutamine derivative under liberation of ammonia. See therefore schemes 1 and 2.
Scheme 1: Cyclization of glutamine by QC peptide
Figure imgf000005_0001
Scheme 2: Cyclization of L-homoglutamine by QC peptide
Figure imgf000006_0001
The term "EC" as used herein comprises the side activity of QC and QC-like enzymes as glutamate cyclase (EC), further defined as EC activity.
The expression "QC/EC" refers to the glutaminyi cyclase, which has at least one of QC or EC activity, preferably both, QC and EC activity.
The term "EC activity" as used herein is defined as intramolecular cyclization of N- terminal glutamate residues into pyroglutamic acid (pGlu*) by QC. See therefore scheme 3.
Scheme 3: ^-terminal cyclization of uncharged glutamyl peptides by QC (EC)
Figure imgf000006_0002
The term "QC-inhibitor" "glutaminyi cyclase inhibitor" is generally known to a person skilled in the art and means enzyme inhibitors, which inhibit the catalytical activity of glutaminyi cyclase (QC) and/or its glutamyl cyclase (EC) activity.
The term "subject" as used herein, refers to an animal, preferably a mammal, most preferably a human, who has been the object of treatment, observation or experiment.
The term "therapeutically effective amount" as used herein, means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue system, animal or human being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated.
As used herein, the term "pharmaceutically acceptable" embraces both human and veterinary use: for example the term "pharmaceutically acceptable" embraces a veterinarily acceptable compound or a compound acceptable in human medicine a health care.
Throughout the description and the claims the expression "acyl" can denote a Cι-2o acyl residue, preferably a C1-8 acyl residue and especially preferred a C -4 acyl residue; "cycloalkyl" can denote a C3-12 cycloalkyl residue, preferably a C4, C5 or C6 cycloalkyl residue; and "a carbocycle" can denote a C3-12 a carbocycle residue, preferably a C4, C5 or Cβ a carbocycle residue. "Heteroaryl" is defined as an aryl residue, wherein 1 to 4, and more preferably 1 , 2 or 3 ring atoms are replaced by heteroatoms like N, S or O. "A heterocycle" is defined as a cycloalkyl residue, wherein 1 , 2 or 3 ring atoms are replaced by heteroatoms like N, S or O. "Peptides" are selected from dipeptides to decapeptides, preferred are dipeptides, tripeptides, tetrapeptides and pentapeptides. The amino acids for the formation of the "peptides" can be selected from those listed above.
Throughout the description and the claims the expression "alkyl" can denote a C1-50 alkyl group, preferably a C6-3o alkyl group, especially a Cβ-12 alkyl group; for example, an alkyl group may be a methyl, ethyl, propyl, isopropyl or butyl group. The expression "alk", for example in the expression "alkoxy", and the expression "alkan", for example in the expression "alkanoyl", are defined as for "alkyl"; aromatic compounds are preferably substituted or optionally unsubstituted phenyl, benzyl, naphthyl, biphenyl or anthracene groups, which preferably have at least 8 C atoms; the expression "alkenyl" can denote a C2-10 alkenyl group, preferably a C2-6 alkenyl group, which has the double bond(s) at any desired location and may be substituted or unsubstituted; the expression "alkynyl" can denote a C2-ιo alkynyl group, preferably a C2-6 alkynyl group, which has the triple bond(s) at any desired location and may be substituted or unsubstituted.
The expression "substituted" or substituent can denote any desired substitution by one or more, preferably one or two, alkyl, alkenyl, alkynyl, mono- or multi-valent acyl, alkanoyl, alkoxyalkanoyl or alkoxyalkyl groups; the afore-mentioned substituents may in turn have one or more (but preferably zero) alkyl, alkenyl, alkynyl, mono- or multi-valent acyl, alkanoyl, alkoxyalkanoyl or alkoxyalkyl groups as side groups; organic amines, amides, alcohols or acids, each having from 8 to 50 C atoms, preferably from 10 to 20 C atoms, can have the formulae (alkyl)2N- or alkyl-NH-, -CO-N(alkyl)2 or -CO-NH(alkyl), - alkyl-OH or -alkyl-COOH.
Furthermore, the expression "substituted" or "substituent" can denote one or two of each, branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle; the afore-mentioned substituents may in turn have one or more branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle as side group(s); all herein before mentioned chains, residues or side groups may contain one or more, preferably one or two, epoxy moiety(ies) and one or more, preferably one or two, substituted or unsubstituted aziridine(s), whereas the substitution is characterized again as R^ which is described above; all chains, residues or side groups may be substituted by one or more F, Cl, Br, I, NH2, NO, N02, CN atoms or groups, isocyanide(s), cyanate(s), isocyanate(s), fulminate(s), thiocyanate(s), isothiocyanate(s), selenocyanate(s) and isoselenocyanate(s), thio acids of sulphur with empirical formulae -S2H, -S2OH, -S3H, - S2O2H, -S3OH, and -S H and their derivatives, whereas the substitution is characterized as Ri; azonic acid(s), azinic acid(s), sulphonic acid(s) (S02H), sulphur acid(s) (SQ3H) and their esters, whereas the ester residue(s) is characterized as Ri; phosphinous acid(s), phosphonous acid(s), phosphinic acid(s), phosphonic acid(s), their replaced modifications like phosphinothioic O-acid(s), phosphinothioic S-acid(s), phosphinimidic acid(s), phosphonothioic 0,0'-acid(s), phosphonothioic 0,S'-acid(s), phosphonimidothioic acid(s) and their esters, whereas the ester residue(s) is characterized as Ri.
Furthermore, all afore-mentioned chains, residues or side groups may contain one or more, preferably one, two or three alcohol(s), acid(s), aldehyde(s) or ketone(s), phosphane(s), phosphorane(s), sulfoxides (SO), sulfones (S02), their selenium or tellurium analogues named selenoxide and selenone, sulfonic anhydride(s) [(S02)2θ] and sulphonic anhydride(s) [(SO)2θ], hydrazide(s), Λ/-Oxides of azo compounds; as well as amine(s), amide(s), ester(s), ether(s) or sulfonamid(e), phosphane(s) or phosphorane(s), having the formulae -NHRi or -N(Ri)2, -CON(Ri)2 or -CONHRi, -CO- ORι, Ri-O-Ri, -Sθ2N(Ri)2 or -S02NHRi, -PHR^ -P(Ri)2, -PH3R1, -PH2(Rι)2, -PH(Ri)3, - P(Rι)4, whereas Ri is described above; as well as the corresponding thio analogues of the in advance described residues, where the oxygen is replaced by sulphur, for example thiol(s), thioaldehyde(s) and thioketone(s).
Amino acids which can be used in the present invention are L and D-amino acids, N- methyl-amino acids, aza-amino acids; allo- and tøreo-forms of lie and Thr, which can, e.g. be α-, β- or ω-amino acids, whereof α-amino acids are preferred.
Examples of amino acids are: aspartic acid (Asp), glutamic acid (Glu), arginine (Arg), lysine (Lys), histidine (His), glycine (Gly), serine (Ser), cysteine (Cys), threonine (Thr), asparagine (Asn), glutamine (Gin), tyrosine (Tyr), alanine (Ala), proline (Pro), valine (Val), isoleucine (lie), leucine (Leu), methionine (Met), phenylalanine (Phe), tryptophan (Trp), hydroxyproline (Hyp), beta-alanine (beta-Ala), 2-aminooctanoic acid (Aoa), acetidine-(2)-carboxylic acid (Ace), pipecolic acid (Pip), 3-aminopropionic acid, 4-aminobutyric acid and so forth, alpha- aminoisobutyric acid (Aib), sarcosine (Sar), ornithine (Orn), citrulline (Cit), homoarginine (Har), t-butylalanine (f-butyl-Ala), t-butylglycine (f-butyl-Gly), N-methylisoleucine (N- Melle), phenylglycine (Phg), cyclohexylalanine (Cha), norleucine (Nle), cysteic acid (Cya) and methionine sulfoxide (MSO), acetyl-Lys, modified amino acids such as phosphoryl-serine (Ser(P)), benzyl-serine (Ser(Bzl)) and phosphoryl-tyrosine (Tyr(P)), 2- aminobutyric acid (Abu), aminoethylcysteine (AECys), carboxymethylcysteine (Cmc), dehydroalanine (Dha), dehydroamino-2-butyric acid (Dhb), carboxyglutaminic acid (Gla), homoserine (Hse), hydroxylysine (Hyl), c/s-hydroxyproline (c/sHyp), trans- hydroxyproline (transHyp), isovaline (Iva), pyroglutamic acid (Pyr), norvaline (Nva), 2- aminobenzoic acid (2-Abz), 3-aminobenzoic acid (3-Abz), 4- aminobenzoic acid (4-Abz), 4-(aminomethyl)benzoic acid (Amb), 4-(aminomethyl)cyclohexanecarboxylic acid (4- Amc), Penicillamine (Pen), 2-amino-4-cyanobutyric acid (Cba), cycloalkane-carboxylic aicds. Examples of tσ-amino acids are e.g.: 5-Ara (aminoraleric acid), 6-Ahx (aminohexanoic acid), 8-Aoc (aminooctanoic aicd), 9-Anc (aminovanoic aicd), 10-Adc (aminodecanoic acid), 11-Aun (aminoundecanoic acid), 12-Ado (aminododecanoic acid). Further amino acids are: indanylglycine (Igl), indoline-2-carboxylic acid (Idc), octahydroindole-2-carboxylic acid (Oic), diaminopropionic acid (Dpr), diaminobutyric acid (Dbu), naphtylalanine (1-Nal) and (2-Nal), 4-aminophenylalanine (Phe(4-NH2)), 4- benzoylphenylalanine (Bpa), diphenylalanine (Dip), 4-bromophenylalanine (Phe(4-Br)), 2-chlorophenylalanine (Phe(2-CI)), 3-chlorophenylalanine (Phe(3-CI)), 4- chlorophenylalanine (Phe(4-CI)), 3,4-chlorophenylalanine (Phe (3,4-C )), 3- fluorophenylalanine (Phe(3-F)), 4-fluorophenylalanine (Phe(4-F)), 3,4- fluorophenylalanine (Phe(3,4-F2)), pentafluorophenylalanine (Phe(F5)), 4- guanidinophenylalanine (Phe(4-guanidino)), homophenylalanine (hPhe), 3- jodophenylalanine (Phe(3-J)), 4-jodophenylalanine (Phe(4-J)), 4-methylphenylalanine (Phe(4-Me)), 4-nitrophenylalanine (Phe-4-NO2)), biphenylalanine (Bip), 4- phosphonomethylphenylalanine (Pmp), cyclohexylglycine (Ghg), 3-pyridinylalanine (3- Pal), 4-pyridinylalanine (4-Pal), 3,4-dehydroproline (A-Pro), 4-ketoproline (Pro(4-keto)), thioproline (Thz), isonipecotic acid (Inp), 1 ,2,3,4,-tetrahydroisoquinolin-3-carboxylic acid (Tic), propargylglycine (Pra), 6-hydroxynorleucine (NU(6-OH)), homotyrosine (hTyr), 3- jodotyrosine (Tyr(3-J)), 3,5-dijodotyrosine (Tyr(3,5-J2)), methyltyrosine (Tyr(Me)), 2', 6'- dimethyltyrosine (Dmt), 3-N02-tyrosine (Tyr(3-N02)), phosphotyrosine (Tyr(P03H2)), alkylglycine, 1-aminoindane-1 -carboxylic acid, 2-aminoindane-2-carboxylic acid (Aic), 4- amino-methylpyrrol-2-carboxylic acid (Py), 4-amino-pyrrolidine-2-carboxylic acid (Abpc), 2-aminotetraline-2-carboxylic acid (Ate), diaminoacetic acid (Gly(NH2)), diaminobutyric acid (Dab), 1 ,3-dihydro-2H-isoinole-carboxylic acid (Disc), homocylcohexylalanine (hCha), homophenylalanine (hPhe or Hof), frans-3-phenyl-azetidine-2-carboxylic acid, 4-phenyl-pyrrolidine-2-carboxylic acid, 5-phenyl-pyrrolidine-2-carboxylic acid, 3- pyridylalanine (3-Pya), 4-pyridylalanine (4-Pya), styrylalanine, tetrahydroisoquinoline-1- carboxylic acid (Tiq), 1 ,2,3,4-tetrahydronorharmane-3-carboxylic acid (Tpi), β-(2- thienryl)-alanine (Tha).
"Peptides" are selected from dipeptides to decapeptides, preferred are dipeptides, tripeptides, tetrapeptides and pentapeptides. The amino acids for the formation of the "peptides" can be selected from those listed above.
An "aza-amino acid" is defined as an amino acid where the chiral α-CH group is replaced by a nitrogen atom, whereas an "aza-peptide" is defined as a peptide, in which the chiral α-CH group of one or more amino acid residues in the peptide chain is replaced by a nitrogen atom.
Other amino acid substitutions for those encoded in the genetic code can also be included in peptide compounds within the scope of the invention and can be classified within this general scheme. Proteinogenic amino acids are defined as natural protein- derived α-amino acids. Non-proteinogenic amino acids are defined as all other amino acids, which are not building blocks of common natural proteins.
"Peptide mimetics" per se are known to a person skilled in the art. They are preferably defined as compounds which have a secondary structure like a peptide and optionally further structural characteristics; their mode of action is largely similar or identical to the mode of action of the native peptide; however, their activity (e.g. as an antagonist or inhibitor) can be modified as compared with the native peptide, especially vis a vis receptors or enzymes. Moreover, they can imitate the effect of the native peptide (agonist). Examples of peptide mimetics are scaffold mimetics, non-peptidic mimetics, peptoides, peptide nucleic acids, oligopyrrolinones, vinylogpeptides and oligocarbamates. For the definitions of these peptide mimetics see Lexikon der Chemie, Spektrum Akademischer Verlag Heidelberg, Berlin, 1999. The aim for using these mimetic structures is increasing the activity, increasing the selectivity to decrease side effects, protect the compound against enzymatic degradation for prolongation of the effect.
Stereoisomers:
All possible stereoisomers of the claimed compounds are included in the present invention.
Where the compounds according to this invention have at least one chiral center, they may accordingly exist as enantiomers. Where the compounds possess two or more chiral centers, they may additionally exist as diastereomers. It is to be understood that all such isomers and mixtures thereof are encompassed within the scope of the present invention.
Preparation and isolation of stereoisomers:
Where the processes for the preparation of the compounds according to the invention give rise to a mixture of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. The compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution. The compounds may, for example, be resolved into their components enantiomers by standard techniques, such as the formation of diastereomeric pairs by salt formation with an optically active acid, such as (-)-di-p-toluoyl-d-tartaric acid and/or (+)-di-p-toluoyl-l-tartaric acid followed by fractional crystallization and regeneration of the free base. The compounds may also resolved by formation of diastereomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary. Alternatively, the compounds may be resolved using a chiral HPLC column.
Pharmaceutically acceptable salts:
In view of the close relationship between the free compounds and the compounds in the form of their salts, whenever a compound is referred to in this context, a corresponding salt is also intended, provided such is possible or appropriate under the circumstances. The pharmaceutically acceptable salt generally takes a form in which an amino acids basic side chain is protonated with an inorganic or organic acid. Representative organic or inorganic acids include hydrochloric, hydrobromic, perchloric, sulfuric, nitric, phosphoric, acetic, propionic, glycolic, lactic, succinic, maleic, fumaric, malic, tartaric, citric, benzoic, mandelic, methanesulfonic, hydroxyethanesulfonic, benzenesulfonic, oxalic, pamoic, 2-naphthalenesulfonic, p-toulenesulfonic, cyclohexanesulfamic, salicylic, saccharinic or trifluoroacetic acid. All pharmaceutically acceptable acid addition salt forms of the compounds of the present invention are intended to be embraced by the scope of this invention.
Polymorph crystal forms:
Furthermore, some of the crystalline forms of the compounds may exist as polymorphs and as such are intended to be included in the present invention. In addition, some of the compounds may form solvates with water (i.e. hydrates) or common organic solvents, and such solvates are also intended to be encompassed within the scope of this invention. The compounds, including their salts, can also be obtained in the form of their hydrates, or include other solvents used for their crystallization.
Prodrugs:
The present invention further includes within its scope prodrugs of the compounds of this invention. In general, such prodrugs will be functional derivatives of the compounds which are readily convertible in vivo into the desired therapeutically active compound. Thus, in these cases, the methods of treatment of the present invention, the term "administering" shall encompass the treatment of the various disorders described with prodrug versions of one or more of the claimed compounds, but which converts to the above specified compound in vivo after administration to the subject. Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in "Design of Prodrugs", ed. H. Bundgaard, Elsevier, 1985 and the patent applications DE 198 28 113, DE 198 28 114, WO 99/67228 and WO 99/67279 which are fully incorporated herein by reference.
Protective Groups: During any of the processes for preparation of the compounds of the present invention, it may be necessary and/or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W. McOmie, Plenum Press, 1973; and T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991 , fully incorporated herein by reference. The protecting groups may be removed at a convenient subsequent stage using methods known from the art.
As used herein, the term "composition" is intended to encompass a product comprising the claimed compounds in the therapeutically effective amounts, as well as any product which results, directly or indirectly, from combinations of the claimed compounds.
Carriers and Additives for galenic formulations:
Thus, for liquid oral preparations, such as for example, suspensions, elixirs and solutions, suitable carriers and additives may advantageously include water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents and the like; for solid oral preparations such as, for example, powders, capsules, gelcaps and tablets, suitable carriers and additives include starches, sugars, diluents, granulating agents, lubricants, binders, disintegrating agents and the like.
Carriers, which can be added to the mixture, include necessary and inert pharmaceutical excipients, including, but not limited to, suitable binders, suspending agents, lubricants, flavorants, sweeteners, preservatives, coatings, disintegrating agents, dyes and coloring agents.
Soluble polymers as targetable drug carriers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamidephenol, polyhydroxyethylaspartamide- phenol, or polyethyleneoxidepolyllysine substituted with palmitoyl residue. Furthermore, the compounds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polyactic acid, polyepsilon caprolactone, polyhydroxy butyeric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and cross-linked or amphipathic block copolymers of hydrogels.
Suitable binders include, without limitation, starch, gelatin, natural sugars such as glucose or betalactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth or sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride and the like.
Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum and the like.
Peptide Sequences
The peptides mentioned and used herein have the following sequences:
Aβ(1-42):
Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-His-His-Gln-Lys-Leu-Val-Phe-Phe-
Ala-Glu-Asp-Val-Gly-Ser-Asn-Lys-Gly-Ala-lle-lle-Gly-Leu-Met-Val-Gly-Gly-Val-Val-lle-
Ala
Aβ(1-40):
Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-His-His-Gln-Lys-Leu-Val-Phe-Phe- Ala-Glu-Asp-Val-Gly-Ser-Asn-Lys-Gly-Ala-lle-lle-Gly-Leu-Met-Val-Gly-Gly-Val-Val
Aβ(3-42):
Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-His-His-Gln-Lys-Leu-Val-Phe-Phe-Ala-Glu- Asp-Val-Gly-Ser-Asn-Lys-Gly-Ala-lle-lle-Gly-Leu-Met-Val-Gly-Gly-Val-Val-lle-Ala
Aβ(3-40):
Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-His-His-Gln-Lys-Leu-Val-Phe-Phe-Ala-Glu- Asp-Val-Gly-Ser-Asn-Lys-Gly-Ala-lle-lle-Gly-Leu-Met-Val-Gly-Gly-Val-Val
Aβ(1-11)a:
Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-NH2 Aβ(3-11)a:
Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-NH2
Aβ(1-21)a:
Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-His-His-Gln-Lys-Leu-Val-Phe-Phe- Ala-NH2
Aβ(3-21)a:
Glu-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-His-His-Gln-Lys-Leu-Val-Phe-Phe-Ala-NH2
Gln3-Aβ(3-40):
Gln-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-His-His-Gln-Lys-Leu-Val-Phe-Phe-Ala-Glu- Asp-Val-Gly-Ser-Asn-Lys-Gly-Ala-lle-lle-Gly-Leu-Met-Val-Gly-Gly-Val-Val
Gln3-Aβ(3-21)a:
Gln-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-Val-His-His-Gln-Lys-Leu-Val-Phe-Phe-Ala-NH2
Gln3-Aβ(1-11)a:
Asp-Ala-Gln-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-NH2
Gln3-Aβ(3-11)a:
Gln-Phe-Arg-His-Asp-Ser-Gly-Tyr-Glu-NH2
Summary of the invention
The present invention provides compounds that act as inhibitors of glutaminyi cyclase (QC, EC 2.3.2.5). Those compounds are represented by the general formulae 1 to 6.
Figure imgf000016_0001
formula 1 formula 2 formula 3
Figure imgf000017_0001
formula 4 formula 5
Figure imgf000017_0002
Physiological substrates of QC in mammals are, e.g. [Glu3] amyloid β-protein (3-40/42), [Gin3] amyloid β-protein (3-40/42), Gastrin, Neurotensin, FPP, CCL 2, CCL 7, CCL 8, CCL 16, CCL 18, Fractalkine, Orexin A, [Gln3]-glucagon(3-29) and [Gln5]-substance P(5-11). The compounds according to the present invention and pharmaceutical compositions comprising at least one compound according to the present invention are useful for the treatment of conditions that can be treated by modulation of QC activity.
By administering inhibitors of QC/EC activity to a mammal it can be possible to prevent or alleviate or treat neuronal disorders (Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
Furthermore, by administration of a compound according to the present invention to a mammal it can be possible to stimulate the proliferation of myeloid progenitor cells.
In addition, the administration of a QC inhibitor according to the present invention can lead to suppression of male fertility.
In a preferred embodiment, the present invention provides the use of inhibitors of QC/EC activity in combination with other agents, especially for the treatment of neuronal disorders. Detailed description of the invention
The present invention provides compounds having the general formula 1 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
Figure imgf000018_0001
formula 1 wherein n is 1 , 2, 3 or 4, preferably 2 or 3, especially 2, and A can be a saturated or unsaturated heterocycle and may be substituted or unsubstituted, and wherein Ri is H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri optionally being substituted independently of each other.
In addition, the present invention relates to compounds which can be described generally by the the general formula 2 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
Figure imgf000018_0002
formula 2 wherein Ri, R2 and R3 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R and R3 optionally being substituted independently of each other. Furthermore, the present invention relates to compounds which can be described generally by the general formula 3 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
Figure imgf000019_0001
formula 3 wherein n is 1 , 2, 3 or 4, preferably 2 or 3, especially 2, and A can be a saturated or unsaturated heterocycle and may be substituted or unsubstituted, and wherein Ri and R2 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri and R2 optionally being substituted independently of each other.
Furthermore, the present invention relates to compounds which can be described generally by the general formula 4 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
Figure imgf000019_0002
formula 4 wherein n is 1, 2, 3 or 4, preferably 2 or 3, especially 2, and A can be a saturated or unsaturated heterocycle and may be substituted or unsubstituted, and wherein Ri, R2 and R3 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R2 and R3 optionally being substituted independently of each other. Furthermore, the present invention relates to compounds which can be described generally by the general formula 5 and the pharmaceutically acceptable salts thereof, including all stereoisomers:
Figure imgf000020_0001
formula 5 wherein Ri, R2, R3, R and R5 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R2, R3> 4 and R optionally being substituted independently of each other.
Furthermore, the present invention relates to compounds which can be described generally by the general formula 6 or the pharmaceutically acceptable salts thereof, including all stereoisomers:
Figure imgf000020_0002
formula 6 wherein Ri, R2, R3, R4 and R5 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R2, 3, R4 and R5 optionally being substituted independently of each other.
Preferred structures relate to formula 2a:
Figure imgf000020_0003
formula 2a
• wherein A is a branched or unbranched C C7 alkyl chain, a branched or unbranched Cι-C7 alkenyl chain, a branched or unbranched Cι-C7 alkynyl chain,
or wherein A is a compound selected from the group consisting of :
Figure imgf000021_0001
• wherein R6-R10 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle , preferably H or methyl,
• wherein n and n1 are independently 1 - 5, m is 1 - 5 , o is 0 - 4,
Preferably A is a C3 alkyl chain, a C3 methyl branched alkyl chain, cycloalkyl- 1 ,1- dimethyl of formula (IV) with m = 1-4, 1 ,4-dimethylphenyl or 1 ,3-dimethylphenyl; and
• wherein B is a compound selected from the group consisting of
Figure imgf000022_0001
(VI) (VII)
Figure imgf000022_0002
• wherein D and E are a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle,
Preferably D and E are a substituted phenyl, wherein substitution means oxyalkyl, thioalkyl, halogenyl, or carboxylic acid alkyl ester or aryl ester. Further preferred are compounds, wherein D and E are a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine.
• wherein Z is CH or N.
In a preferred embodiment, Z is N.
• wherein X can be O, S, N-CN, with the proviso for formulas (VIII) and (IX) that, if Z = CH, X is O or S,
• wherein X1, X2 and X3 are independently O or S,
In a preferred embodiment, X is S.
• wherein Y is O or S,
• wherein R11-R14 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, halogenyl, oxyalkyl, thioalkyl, carboxyl, carboxylic acid ester, carbonyl, carbamide, carbimide, thiocarbamide or thiocarbonyl.
In a preferred embodiment, R11 and R14are H.
In a further preferred embodiment, R12 and R13 are independently oxyalkyl or thioalkyl, halogenyl, or carboxylic acid alkyl ester or phenyl, or R12 and R13 are connected to form a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine,
• wherein R15 and R16 are independently H or a branched or unbranched alkyl chain, or a branched or unbranched alkenyl chain.
In a preferred embodiment, at least one of R15 and R 6 is H. Most preferably, R15 and R16 are both H.
• wherein R17 and R18 are independently of each other H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl or can be connected to form a carbocycle with up to 6 ring atoms.
In a preferred embodiment, one of R17 and R18 is H and the other is Me.
Further preferred are compounds wherein one of R17 and R18 is H and the other is phenyl.
In a further preferred embodiment, R17 and R18 may form a carbocycle with up to 6 ring atoms.
• wherein n is 0 or 1 ,
all of the above residues being optionally substituted independently of each other.
Furthermore, the present invention provides the use of compounds of the formula 2a
N^\ i N-A-B
formula 2a
for the preparation of a medicament for the treatment of diseases selected from the group consisting of Alzheimer's disease, Down Syndrome, Parkinson disease, Chorea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia, • wherein A is a branched or unbranched Cι-C7 alkyl chain, a branched or unbranched C C alkenyl chain, a branched or unbranched Cι-C7 alkynyl chain,
or wherein A is a compound selected from the group consisting of :
Figure imgf000025_0001
• wherein R6-R10 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle , preferably H or methyl,
• wherein n and n1 are independently 1 - 5, m is 1 - 5 , o is 0 - 4,
Preferably A is a C3 alkyl chain, a C3 methyl branched alkyl chain, cycloalkyl-1 ,1- dimethyl of formula (IV) with m = 1-4, 1 ,4-dimethylphenyl or 1 ,3-dimethylphenyl; and
wherein B is a compound selected from the group consisting of
Figure imgf000026_0001
(VI) (VII)
Figure imgf000026_0002
(XIV)
• wherein D and E are a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle,
Preferably D and E are a substituted phenyl, wherein substitution means oxyalkyl, thioalkyl, halogenyl, carboxylic acid alkyl ester or aryl ester. Further preferred are compounds, wherein D and E are a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine.
• wherein Z is CH or N.
In a preferred embodiment, Z is N.
wherein X can be O, S, N-CN, with the proviso for formulas (VIII) and (IX) that, if Z = CH, X is O or S,
• wherein X1, X and X3 are independently O or S with the proviso for compound (XIV) that at least one of X2 and X3 must be S, In a preferred embodiment, X is S.
• wherein Y is O or S, with the proviso that Y may not be O when the carbocycle formed by R17 and R18 has 3 members in the ring.
• wherein R1 -R14 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, halogenyl, oxyalkyl, thioalkyl, carboxyl, carboxylic acid ester, carbonyl, carbamide, carbimide, thiocarbamide or thiocarbonyl.
In a preferred embodiment, R11 and R14are H.
In a further preferred embodiment, R12 and R13 are independently oxyalkyl or thioalkyl, halogenyl, or carboxylic acid alkyl ester or phenyl, or R12 and R13 are connected to form a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine,
• wherein R15 and R16 are independently H or a branched or unbranched alkyl chain, or a branched or unbranched alkenyl chain.
In a preferred embodiment, one of R15 and R16 is H. Most preferably, R15 and R16 are both H.
• wherein R17 and R18 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl or can be connected to form a carbocycle with up to 6 ring atoms.
In a preferred embodiment, one of R17 and R18 is H and the other is Me.
Further preferred are compounds wherein one of R17 and R18 is H and the other is phenyl.
In a further preferred embodiment, R17 and R18 may form a carbocycle with up to 6 ring atoms.
• wherein n is 0 or 1 ,
all of the above residues being optionally substituted independently of each other.
Physiological substrates of QC in mammals are, e.g. Aβ3-40/42, [Gln3]Aβ3-40/42, [Glu11]Aβ 11-40/42, [Gin11]Aβ11-40/42, [Gln1]Gastrins (17 and 34), [Gln1]Neurotensin, [Gln1]FPP, [Gln1]TRH, [Gln1]GnRH, [Gln1]CCL 2, [Gln1]CCL 7, [Gln1]CCL 8, [Gln1]CCL 16, [Gln1]CCL 18, [Gln1]ELA, [Gln1]Fractalkine, [Gln1]Orexin A, [Gln3]-glucagon(3-29) and [Gln5]-substance P(5-11). For further details see table 2. The compounds and/or combinations according to the present invention and pharmaceutical compositions comprising at least one inhibitor of QC are useful for the treatment of conditions that can be treated by modulation of QC/EC activity. Table 2: Amino acid sequences of physiological active peptides with an N- terminal glutamine residue
Figure imgf000029_0001
Figure imgf000030_0001
Figure imgf000031_0001
Figure imgf000032_0001
Transepithelial transducing cells, particularly the gastrin (G) cell, co-ordinate gastric acid secretion with the arrival of food in the stomach. Recent work showed that multiple active products are generated from the gastrin precursor, and that there are multiple control points in gastrin biosynthesis. Biosynthetic precursors and intermediates (progastrin and Gly-gastrins) are putative growth factors; their products, the amidated gastrins, regulate epithelial cell proliferation, the differentiation of acid-producing parietal cells and histamine-secreting enterochromaffin-like (ECL) cells, and the expression of genes associated with histamine synthesis and storage in ECL cells, as well as acutely stimulating acid secretion. Gastrin also stimulates the production of members of the epidermal growth factor (EGF) family, which in turn inhibit parietal cell function but stimulate the growth of surface epithelial cells. Plasma gastrin concentrations are elevated in subjects with Helicobacter pylori, who are known to have increased risk of duodenal ulcer disease and gastric cancer (Dockray, G.J. 1999 J Physiol 15315-324).
The peptide hormone gastrin, released from antral G cells, is known to stimulate the synthesis and release of histamine from ECL cells in the oxyntic mucosa via CCK-2 receptors. The mobilized histamine induces acid secretion by binding to the H(2) receptors located on parietal cells. Recent studies suggest that gastrin, in both its fully amidated and less processed forms (progastrin and glycine-extended gastrin), is also a growth factor for the gastrointestinal tract. It has been established that the major trophic effect of amidated gastrin is for the oxyntic mucosa of stomach, where it causes increased proliferation of gastric stem cells and ECL cells, resulting in increased parietal and ECL cell mass. On the other hand, the major trophic target of the less processed gastrin (e.g. glycine-extended gastrin) appears to be the colonic mucosa (Koh, T.J. and Chen, D. 2000 Regul Pept 9337-44).
Neurotensin (NT) is a neuropeptide implicated in the pathophysiology of schizophrenia that specifically modulates neurotransmitter systems previously demonstrated to be misregulated in this disorder. Clinical studies in which cerebrospinal fluid (CSF) NT concentrations have been measured revealed a subset of schizophrenic patients with decreased CSF NT concentrations that are restored by effective antipsychotic drug treatment. Considerable evidence also exists concordant with the involvement of NT systems in the mechanism of action of antipsychotic drugs. The behavioral and biochemical effects of centrally administered NT remarkably resemble those of systemically administered antipsychotic drugs, and antipsychotic drugs increase NT neurotransmission. This concatenation of findings led to the hypothesis that NT functions as an endogenous antipsychotic. Moreover, typical and atypical antipsychotic drugs differentially alter NT neurotransmission in nigrostriatal and mesolimbic dopamine terminal regions, and these effects are predictive of side effect liability and efficacy, respectively (Binder, E. B. et al. 2001 Biol Psychiatry 50856-872).
Fertilization promoting peptide (FPP), a tripeptide related to thyrotrophin releasing hormone (TRH), is found in seminal plasma. Recent evidence obtained in vitro and in vivo showed that FPP plays an important role in regulating sperm fertility. Specifically, FPP initially stimulates nonfertilizing (uncapacitated) spermatozoa to "switch on" and become fertile more quickly, but then arrests capacitation so that spermatozoa do not undergo spontaneous acrosome loss and therefore do not lose fertilizing potential. These responses are mimicked, and indeed augmented, by adenosine, known to regulate the adenylyl cyclase (AC)/cAMP signal transduction pathway. Both FPP and adenosine have been shown to stimulate cAMP production in uncapacitated cells but inhibit it in capacitated cells, with FPP receptors somehow interacting with adenosine receptors and G proteins to achieve regulation of AC. These events affect the tyrosine phosphorylation state of various proteins, some being important in the initial "switching on," others possibly being involved in the acrosome reaction itself. Calcitonin and angiotensin II, also found in seminal plasma, have similar effects in vitro on uncapacitated spermatozoa and can augment responses to FPP. These molecules have similar effects in vivo, affecting fertility by stimulating and then maintaining fertilizing potential. Either reductions in the availability of FPP, adenosine, calcitonin, and angiotensin II or defects in their receptors contribute to male infertility (Fraser, L.R. and Adeoya-Osiguwa, S. A. 2001 Vitam Horm 63, 1-28).
CCL2, CCL7, CCL8, CCL16, CCL18 and fractalkine play an important role in pathophysiological conditions, such as suppression of proliferation of myeloid progenitor cells, neoplasia, inflammatory host responses, cancer, psoriasis, rheumatoid arthritis, atherosclerosis, humoral and cell-mediated immunity responses, leukocyte adhesion and migration processes at the endothelium.
Several cytotoxic T lymphocyte peptide-based vaccines against hepatitis B, human immunodeficiency virus and melanoma were recently studied in clinical trials. One interesting melanoma vaccine candidate alone or in combination with other tumor antigens, is the decapeptide ELA. This peptide is a Melan-A/MART-1 antigen immunodominant peptide analog, with an N-terminal glutamic acid. It has been reported that the amino group and gamma-carboxylic group of glutamic acids, as well as the amino group and gamma-carboxamide group of glutamines, condense easily to form pyroglutamic derivatives. To overcome this stability problem, several peptides of pharmaceutical interest have been developed with a pyroglutamic acid instead of N- terminal glutamine or glutamic acid, without loss of pharmacological properties. Unfortunately compared with ELA, the pyroglutamic acid derivative (PyrELA) and also the N-terminal acetyl-capped derivative (AcELA) failed to elicit cytotoxic T lymphocyte (CTL) activity. Despite the apparent minor modifications introduced in PyrELA and AcELA, these two derivatives probably have lower affinity than ELA for the specific class I major histocompatibility complex. Consequently, in order to conserve full activity of ELA, the formation of PyrELA must be avoided (Beck A. et al. 2001 , J Pept Res 57(6):528-38.). Orexin A is a neuropeptide that plays a significant role in the regulation of food intake and sleep-wakefulness, possibly by coordinating the complex behavioral and physiologic responses of these complementary homeostatic functions. It plays also a role in the homeostatic regulation of energy metabolism, autonomic function, hormonal balance and the regulation of body fluids.
To date, inhibition of human QC was only detected initially for 1 ,10-phenanthroline and reduced 6-methylpterin (Busby, W. H. J. et al. 1987 J Biol Chem 262, 8532-8536). By a comparison of numerous heterocyclic compounds, the present invention demonstrates that imidazole derivatives inhibit the animal QC. Using the continuous assay (for details see example 1), many imidazole derivatives were analyzed concerning their ability to inhibit the human QC as a member of the highly conserved mammalian QCs.
Thus, the present invention provides imidazole and its derivatives and histidine and its derivatives as activity reducing effectors of QC and their characteristics in terms of inhibition type and potency. Structures and K,-values are shown in tables 2 and 3. The results are described in detail in example 2.
Table 2: Inhibitory constants of imidazole derivatives in the human QC catalyzed reaction. Determinations were performed at 30 °C in 0.05 M Tris-HCI pH 8.0, containing 5 mM EDTA.
Compound Kj-value (mM) Structure
core structures imidazole 0.103 ±0.004 benzimidazole 0.138 ±0.005 N-1 derivatives
1-benzylimidazole 0.0071 ±0.0003
1-methylimidazole 0.030 ±0.001
1-vinylimidazole 0.049 ±0.002 oxalic acid diimidazolidide 0.078 ±0.002
N-acetylimidazole 0.107 ±0.003 N-(trimethylsilyl)-imidazole 0.167 ±0.007
N-benzoylimidazole 0.174 ±0.007
1 -(2-oxo-2-phenyl-ethyl)- 0.184 ±0.005 imidazole
1-(3-aminopropyl)-imidazole 0.41 ±0.01
1-phenylimidazole no inhibition
1 ,1 '-sulfonyldiimidazole no inhibition
C-4(5) derivatives
N-omega-acetylhistamine 0.017 ±0.001
L-histidinamide 0.56 ±0.04
H-His-Trp-OH 0.60 ±0.03
L-histidinol 1.53 ±0.12
L-histidine 4.4 ±0.2
4-imidazole-carboxaldehyde 7.6 ±0.7 imidazole-4-carbonic acid 14.5 ±0.6 methylester
L-histamine 0.85 ±0.04
C-4,5 derivatives
5-hydroxymethyl-4-methyl- 0.129 ±0.005 imidazole
4-amino-imidazole-5-carbonic 15.5 ±0.5 acid amide
4,5-diphenyl-imidazole no inhibition
4,5-dicyanoimidazole no inhibition
C-2 derivatives
2-methyl-benzylimidazole 0.165 ±0.004 2-ethyl-4-methyl-imidazole 0.58 ±0.04 2-aminobenzimidazole 1.8 ±0.1 2-chloro-1 H-benzimidazole no inhibition Others
3-(1 H-imidazol-1 -yl)-1 -(3- 0.0025 ±0.0001 methylbenzo[b]thiophene-2- yl)propan-1-one
Figure imgf000037_0001
4-[(1 -methyl-1 H-imidazol-5- 0.0067± 0.0003
Figure imgf000037_0002
4-[2-(1 H-imidazol-1 -yl)- ethoxyjbenzoic acid 0.0034 ±0,0001
Figure imgf000037_0003
3-[3-(1 H-imidazol-1 -yl)propyl]- 2-thioxoimidazolidin-4-one 0.00041 ±0.00001
Figure imgf000037_0004
5-nitro-2-[2-([{3-(1 H-imidazol-
1-yl-)propyl}amino] 0.0066 ±0,0004 carbonyl)phenyl]furamide
Figure imgf000037_0005
N-(4-chlorophenyl)-N '-[2-(1 H- imidazol-1 -yl)ethyl]thiourea 0.00165 ±0.00007
Figure imgf000038_0001
2-[(5-imidazol-1 -ylmethyl- pyrrolidine-2-carbonyl)- 0,0322 ±0,0007 aminoj-propionic acid methyl
Figure imgf000038_0002
ester
2-[(5-lmidazol-1 -ylmethy 1-2,3- n.d. dihydro-1 H-pyrrole-2- carbonyl)-amino]-propionic
Figure imgf000038_0003
acid methyl ester
lmidazo[ϊ *5a]pyridine 0.0356 ±0.0005
Figure imgf000038_0004
Methyl (2S)-2-{[(2S)-2-amino- 0.164 ±0.004 5-(1 H-imidazol-1 -ylamino)-5- oxopentanoyl]amino}-3- methylbutanoate
Figure imgf000038_0005
Table 3. QC inhibition by L-histamine and its two biological metabolites (also known as fe/e-methyl histamine).
Compound Kj value (mM) Structure
L-histamine 0.85 ±0.04
Figure imgf000039_0001
3-methyl-4-( ?-aminoethyl)-
Figure imgf000039_0002
imidazole
1-methyl-4-(y?-aminoethyl)- n.i. imidazole
Figure imgf000039_0003
Surprisingly, during the characterization of the enzymatic activity it was shown in the present invention that, besides a N-terminal glutaminyi residue, also N-terminal β-homo- glutaminyl residues fulfill properties as substrate of QCs from plants and mammals. The N-terminal β-homo-glutaminyl residue was converted into a five-membered lactam ring by catalysis of human and papaya QC, respectively.
Another preferred embodiment of the present invention comprises screening methods for inhibitors of QC.
A preferred screening method for identifying QC inhibitors from a group of compounds comprises the steps of: a) Contacting said compounds with QC under conditions which would permit binding therebetween; b) Adding a substrate of QC; c) Monitoring the conversion of the substrate or optionally measuring the residual QC activity; and d) Calculating changes in the substrate conversion and/or enzyme activity of QC to identify an activity modifying effector.
Another preferred screening method relates to a method for the identification and selection of inhibitors which interact directly or indirectly with the active-site bound metal ion of QC and comprises the following steps: a) Contacting said compounds with QC under conditions which would permit binding therebetween; b) Adding a substrate of QC which is subject to conversion by QC; c) Monitoring the conversion of the substrate or optionally measuring the residual QC activity; and d) Calculating changes in the substrate conversion and/or enzyme activity of QC wherein changes may be used to identify an activity modifying effector of QC.
Preferred for the use in the above described screening methods are mammalian QC or Papaya QC. Especially preferred is mammalian QC, since the inhibitors identified by these screening methods shall be used for the treatment of diseases in mammals, especially in humans.
By administering a QC-inhibitor and/or a combination according to the present invention to a mammal it can be possible to prevent or alleviate or treat conditions selected from Alzheimer's disease, Down Syndrome, ulcer disease and gastric cancer with or w/o Helicobacter pylori infections, neoplasia, inflammatory host responses, cancer, melanoma, malign metastasis, psoriasis, rheumatoid arthritis, atherosclerosis, leukocyte adhesion and migration processes in the endothelium, impaired food intake, sleep- wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance and impaired regulation of body fluids.
Furthermore, by administration of a QC-inhibitor and/or a combination according to the present invention to a mammal it can be possible to stimulate the proliferation of myeloid progenitor cells.
In addition, the administration of a QC-inhibitor and/or a combination according to the present invention can lead to suppression of male fertility.
In a preferred embodiment, the present invention provides the use of inhibitors of QC/EC activity in combination with inhibitors of DP IV or DP IV-like enzymes for the treatment or alleviation of conditions that can be treated by modulation of QC and/or DP IV activity.
In a preferred embodiment, the present invention provides the use of inhibitors of QC/EC activity in combination with inhibitors of PEP for the treatment or alleviation of conditions that can be treated by modulation of QC/EC and/or PEP activity.
Further preferred for the treatment of neuronal diseases is the use of at least one QC- inhibitor in combination with NPY-receptor-ligands, NPY agonists and/or NPY antagonists.
Further preferred for the treatment of neuronal diseases is the use of at least one QC- inhibitor in combination with at least one acetylcholinesterase (ACE) inhibitor.
The present invention provides pharmaceutical compositions for parenteral, enteral or oral administration, comprising at least one inhibitor of QC (EC) optionally in combination with customary carriers and/or excipients; or comprising at least one inhibitor of QC (EC) in combination with at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor-ligand, optionally in combination with customary carriers and/or excipients. These combinations provide a particularly beneficial effect on behavioral conditions and such combinations are therefore shown to be effective and useful for the treatment of neuronal disorders (Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
Accordingly, the invention provides a method for the treatment of neuronal disorders (Alzheimer's disease, Down Syndrome, Parkinson disease, Corea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep- wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia).
The method comprises either co-administration of a QC-inhibitor and/or at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor- ligand and/or at least one ACE-inhibitor or the sequential administration thereof.
Co-administration includes administration of a formulation which includes at least one QC-inhibitor and/or at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor-ligand and/or at least one ACE-inhibitor or the essentially simultaneous administration of separate formulations of each agent.
In another aspect the invention provides the use of at least one QC-inhibitor and/or at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY- receptor-ligand and/or at least one ACE-inhibitor for use in the manufacture of a composition for the treatment of neuronal disorders. The present invention provides pharmaceutical compositions for parenteral, enteral or oral administration, comprising at least one inhibitor of QC (EC) optionally in combination with customary carriers and/or excipients; or comprising at least one inhibitor of QC in combination with at least one DP IV-inhibitor, optionally in combination with customary carriers and/or excipients.
Suitable inhibitors of prolyl endopeptidase are, e.g. chemical derivatives of proline or small peptides containing terminal prolines. Benzyloxycarbonyl-prolyl-prolinal has been shown to be a specific transition state inhibitor of the enzyme (Wilk, S. and Orloeski, M., J. Neurochem., 41 , 69 (1983), Friedman, et al., Neurochem., 42, 237 (1984)). N- terminal substitutions of L-proline or L-prolylpyrrolidine (Atack, et al., Eur. J. of Pharm., 205, 157-163 (1991), JP 03 56,460, EP 384,341), as well as variations of N- benzyloxycarbonyl (Z) dipeptides containing prolinal at the carboxy terminus have been synthesized as prolyl endopeptidase inhibitors (Nishikata, et al., Chem. Pharm. Bull. 34(7), 2931-2936 (1986), Baker, A. et al., Bioorganic & Medicinal Chem. Letts., 1(11), 585-590 (1991)). Thioproline, thiazolidine, and oxopyrrolidine substitutions of the core structure have been reported to inhibit prolyl endopeptidase (Tsuru, et al., J. Biochem., 94, 1179 (1988), Tsuru, et al., J. Biochem., 104, 580-586 (1988), Saito et al., J. Enz. Inhib. 5, 51-75 (1991), Uchida, I., et al. PCT Int. Appl. WO 90 12,005, JP 03 56,461 , JP 03 56,462). Similarly, various modifications of the carboxy terminal proline have been made, including various fluorinated ketone derivatives (Henning, EP 4,912,127). General syntheses of fluorinated ketone derivatives has been described (Angelastro, M.R., et al., Tetrahedron Letters 33(23), 3265-3268 (1992)). Other compounds such as chloromethyl ketone derivatives of acyl-proline or acylpeptide-proline (Z-Gly-Pro-CH2CI) have been demonstrated to inhibit the enzyme by alkylating the enzyme's active site (Yoshimoto, T., et al., Biochemistry 16, 2942 (1977)).
EP-A-0 286 928 discloses 2-acylpyrrolidine derivatives useful as propyl endopeptidase inhibitors. Further suitable prolyl endopeptidase inhibitors according to the present invention are, e.g. Fmoc-Ala-Pyrr-CN and those listed below:
Figure imgf000044_0001
Figure imgf000044_0002
1-pyrrolidinyl] carbonyl}- phenylcyclopropyl] N-(phenylmethyl)-1 - carbonyl}-2-[(thiazolidin-3- pyrrolidin-carboxamid yl)carbonyl] octahydro- 1H-\ndo\
Further suitable prolyl endopeptidase inhibitors according to the present invention are disclosed in JP 01042465, JP 03031298, JP 04208299, WO 0071144, US 5847155; JP 09040693, JP 10077300, JP 05331072, JP 05015314, WO 9515310, WO 9300361 , EP 0556482, JP 06234693, JP 01068396, EP 0709373, US 5965556, US 5756763, US 6121311 , JP 63264454, JP 64000069, JP 63162672, EP 0268190, EP 0277588, EP 0275482, US 4977180, US 5091406, US 4983624, US 5112847, US 5100904, US 5254550, US 5262431 , US 5340832, US 4956380, EP 0303434, JP 03056486, JP 01143897, JP 1226880, EP 0280956, US 4857537, EP 0461677, EP 0345428, 4JP 02275858, US 5506256, JP 06192298, EP 0618193, JP 03255080, EP 0468469, US 5118811 , JP 05025125, WO 9313065, JP 05201970, WO 9412474, EP 0670309, EP 0451547, JP 06339390, US 5073549, US 4999349, EP 0268281 , US 4743616, EP 0232849, EP 0224272, JP 62114978, JP 62114957, US 4757083, US 4810721 , US 5198458, US 4826870, EP 0201742, EP 0201741 , US 4873342, EP 0172458, JP 61037764, EP 0201743, US 4772587, EP 0372484, US 5028604, WO 9118877, JP 04009367, JP 04235162, US 5407950, WO 9501352, JP 01250370, JP 02207070, US 5221752, EP 0468339, JP 04211648 and WO 9946272, the teachings of which are herein incorporated by reference in their entirety, especially concerning these inhibitors, their definition, uses and their production.
Suitable DP IV-inhibitors are are agents such as tetrahydroisoquinolin-3-carboxamide derivatives, N-substituted 2-cyanopyroles and -pyrrolidines, N-(N'-substituted glycyl)-2- cyanopyrrolidines, N-(substituted glycyl)-thiazolidines, N-(substituted glycyl)-4- cyanothiazolidines, boronyl inhibitors and cyclopropyl-fused pyrrolidines. Inhibitors of dipeptidyl peptidase IV are described in US 6,011 ,155; US 6,107,317; US 6,110,949; US 6,124,305; US 6,172,081; WO 99/61431, WO 99/67278, WO 99/67279, DE 198 34 591 , WO 97/40832, DE 196 16 486 C 2, WO 95/15309, WO 98/19998, WO 00/07617, WO 99/38501 , WO 99/46272, WO 99/38501 , WO 01/68603, WO 01/40180, WO 01/81337, WO 01/81304, WO 01/55105, WO 02/02560, WO 01/34594, WO 02/38541 (Japanese), WO 02/ 083128, WO 03/072556, WO 03/002593, WO 03/000250, WO 03/000180, WO 03/000181 , EP 1 258 476, WO 03/002553, WO 03/002531, WO 03/002530, WO 03/004496, WO 03/004498, WO 03/024942, WO 03/024965, WO 03/033524, WO 03/035057, WO 03/035067, WO 03/037327, WO 03/040174, WO 03/045977, WO 03/055881 , WO 03/057144, WO 03/057666, WO 03/068748, WO 03/068757, WO 03/082817, WO 03/101449, WO 03/101958, WO 03/104229, WO 03/74500, WO 04/007446, WO 04/007468, WO 04/018467, WO 04/018468, WO 04/018469, WO 04/026822, the teachings of which are herein incorporated by reference in their entirety concerning the inhibitors, their production and their use.
Preferred DP IV-inhibitors include valine pyrrolidide (Novo Nordisk), NVP-DPP728A (1-[ [ [ 2-[ {5-cyanopyridin-2-yl}amino]ethyl]amino]acetyl]-2-cyano-(S)-pyrrolidine) (Novartis) as disclosed by Hughes et al., Biochemistry, 38 (36), 11597-11603, 1999, LAF-237 (1- [(3-hydroxy-adamant-1-ylamino)-acetyl]-pyrrolidine-2(S)-carbonitrile); disclosed by Hughes et al., Meeting of the American Diabetes Association 2002, Abstract no. 272 or (Novartis), TSL-225 (tryptophyl-1 ,2,3,4-tetrahydroisoquinoline-3-carboxylic acid), disclosed by Yamada et. al., Bioorg. & Med. Chem. Lett. 8 (1998), 1537-1540, 2- cyanopyrrόlidides and 4-cyanopyrrolidides as disclosed by Asworth et al., Bioorg. & Med. Chem. Lett., 6, No. 22, pp 1163-1166 and 2745-2748 (1996), FE-999011 ( [(2S)-1- ([2'S]-2'-amino-3',3'dimethyl-butanoyl)-pyrrolidine-2-carbonitrile] ), disclosed by Sudre et al., Diabetes 51 (5), pp 1461-1469 (2002) (Ferring), GW-229A (GlaxoSmithKline), disclosed by Randhawa SA, et al, ACS Meeting 2003, 226th:New York (MEDI 91), 815541 (Tanabe/GlaxoSmithKline), MK-431 (Merck & Co), PT-100 (Point Therapeutics) and the compounds disclosed in WO 01/34594 (Guilford), employing dosages as set out in the above references.
For the avoidance of doubt, the examples disclosed in each of the above mentioned publications are specifically incorporated herein by reference in their entirety, as individually disclosed compounds, especially concerning their structure, their definition, uses and their production. Other suitable agents that can be used according to the present invention in combination with QC-inhibitors are NPY, a NPY mimetic or a NPY agonist or antagonist or a ligand of the NPY receptors.
Preferred according to the present invention are antagonists of the NPY receptors.
Suitable ligands or antagonists of the NPY receptors are 3a,4,5,9b-tetrahydro-1h- benz[e]indol-2-yl amine-derived compounds as disclosed in WO 00/68197.
NPY receptor antagonists which may be mentioned include those disclosed in European patent applications EP 0 614 911 , EP 0 747 357, EP 0 747 356 and EP 0 747 378; international patent applications WO 94/17035, WO 97/19911 , WO 97/19913, WO 96/12489, WO 97/19914, WO 96/22305, WO 96/40660, WO 96/12490, WO 97/09308, WO 97/20820, WO 97/20821 , WO 97/20822, WO 97/20823, WO 97/19682, WO 97/25041 , WO 97/34843, WO 97/46250, WO 98/03492, WO 98/03493, WO 98/03494 and WO 98/07420; WO 00/30674, US patents Nos. 5,552,411 ,5,663,192 and 5,567,714; 6,114,336, Japanese patent application JP 09157253; international patent applications WO 94/00486, WO 93/12139, WO 95/00161 and WO 99/15498; US Patent No. 5,328,899; German patent application DE 393 97 97; European patent applications EP 355 794 and EP 355 793; and Japanese patent applications JP 06116284 and JP 07267988, the disclosures in all of which documents are hereby incorporated by reference. Preferred NPY antagonists include those compounds that are specifically disclosed in these patent documents. More preferred compounds include amino acid and non-peptide-based NPY antagonists. Amino acid and non-peptide-based NPY antagonists which may be mentioned include those disclosed in European patent applications EP 0 614 911 , EP 0 747 357, EP 0 747 356 and EP 0 747 378; international patent applications WO 94/17035, WO 97/19911 , WO 97/19913, WO 96/12489, WO 97/19914, WO 96/22305, WO 96/40660, WO 96/12490, WO 97/09308, WO 97/20820, WO 97/20821 , WO 97/20822, WO 97/20823, WO 97/19682, WO 97/25041 , WO 97/34843, WO 97/46250, WO 98/03492, WO 98/03493, WO 98/03494, WO 98/07420 and WO 99/15498 ; US patents Nos. 5,552,411 ,5,663,192 and 5,567,714; and Japanese patent application JP 09157253. Preferred amino acid and non-peptide-based NPY antagonists include those compounds that are specifically disclosed in these patent documents.
Particularly preferred compounds include amino acid-based NPY antagonists. Amino acid-based compounds which may be mentioned include those disclosed in international patent applications WO 94/17035, WO 97/19911 , WO 97/19913, WO 97/19914 or, preferably, WO 99/15498. Preferred amino acid-based NPY antagonists include those that are specifically disclosed in these patent documents, for example BIBP3226 and, especially, (R)-N2-(diphenylacetyl)-(R)-N-[1-(4-hydroxy- phenyl) ethyl] arginine amide (Example 4 of international patent application WO 99/15498).
For the avoidance of doubt, the examples disclosed in each of the above mentioned publications are specifically incorporated herein by reference in their entirety, as individually disclosed compounds, especially concerning their structure, their definition, uses and their production.
Preferred DP IV-inhibitors are dipeptide-like compounds and compounds analogous to dipeptide compounds that are formed from an amino acid and a thiazolidine or pyrrolidine group, and salts thereof, referred to hereinafter as dipeptide-like compounds. Preferably the amino acid and the thiazolidine or pyrrolidine group are bonded with an amide bond. Such compounds are disclosed in WO 99/61431.
Especially suitable for that purpose according to the invention are dipeptide-like compounds in which the amino acid is preferably selected from a natural amino acid, such as, for example, leucine, valine, glutamine, glutamic acid, proline, isoleucine, asparagines and aspartic acid.
The dipeptide-like compounds used according to the invention exhibit at a concentration (of dipeptide compounds) of 10 μM, a reduction in the activity of plasma dipeptidyl peptidase IV or DP IV-analogous enzyme activities of at least 10 %, especially of at least 40 %. Frequently a reduction in activity of at least 60 % or at least 70 % is also required. Preferred agents may also exhibit a reduction in activity of a maximum of 20 % or 30 %. Preferred compounds are N-valyl prolyl, O-benzoyl hydroxy la mine, alanyl pyrrolidine, isoleucyl thiazolidine like L-allo-isoleucyl thiazolidine, L-threo-isoleucyl pyrrolidine and salts thereof, especially the fumaric salts, and L-allo-isoleucyl pyrrolidine and salts thereof. Especially preferred compounds are glutaminyi pyrrolidine and glutaminyi thiazolidine of formulas 8 and 9:
Figure imgf000049_0001
(8)
Figure imgf000049_0002
(9)
Further preferred compounds are given in Table 4.
The salts of the dipeptide-like compounds can be present in a molar ratio of dipeptide (- analogous) component to salt component of 1 : 1 or 2 : 1. Such a salt is, for example, (lle-Thia)2 fumaric acid. Table 4: Structures of further preferred dipeptide compounds
DP IV-inhibitor
H-Asn-pyrrolidine
H-Asn-thiazolidine
H-Asp-pyrrolidine
H-Asp-thiazolidine
H-Asp(NHOH)-pyrrolidine
H-Asp(NHOH)-thiazolidine
H-Glu-pyrrolidine
H-Glu-thiazolidine
H-Glu(NHOH)-pyrrolidine
H-Glu(NHOH)-thiazolidine
H-His-pyrrolidine
H-His-thiazolidine
H-Pro-pyrrolidine
H-Pro-thiazolidine
H-lle-azididine
H-lle-pyrrolidine
H-L-a//o-lle-thiazolidine
H-Val-pyrrolidine
H-Val-thiazolidine
Further preferred DP IV-inhibitors are
(1) Peptide structures as disclosed in WO 03/002593, e.g. f-butyl-Gly-Pro-D-Val, t- butyl-Gly -Pro-Gly, f-butyl-Gly -Pro-lie, f-butyl-Gly -Pro-lie-amide, f-butyl-Gly-Pro- f-butyl-Gly, f-butyl-Gly-Pro-Val,
(2) Peptidylketones as disclosed in WO03/033524, e.g. 2-Methylcarbonyl-1-N-[(L)- Alanyl-(L)-Valinyl]-(2S)-pyrrolidine hydrobromide; 2-Methyl)carbonyl-1 -N-[(L)- Valinyl-(L)-Prolyl-(L)-Valinyl]-(2S)-pyrrolidine hydrobromide; 2-[(Acetyl-oxy- methyl)carbonyl]-1-N-[(L)-Alanyl-(L)-Valinyl]-(2S)-pyrrolidine hydrobromide; 2- [Benzoyl-oxy-methyl)carbonyl]-1-N-[{(L)-AlanylHL)-Valinyl]-(2S)-pyrrolidine hydrobromide; 2-{[(2,6-Dichlorbenzyl)thiomethyl]carbonyl}-1-N-[{(L)-Alanyl}-(L)- Valinyl]-(2S)-pyrrolidine; 2-[Benzoy-loxy-methyl)carbonyl]-1-N-[Glycyl-(L)-Valinyl]- (2S)-pyrrolidine hydrobromide; 2-[([1 ,3]-thiazole-2-yl)carbonyl]-1-N-[{(L)-Alanyl}- (L)-Valinyl]-(2S)-pyrrolidine trifluoracetat; 2-[(benzothiazole-2-yl)carbonyl]-1 -N-[N- {(L)-Alanyl}-(L)-Valinyl]-(2S)-pyrrolidin trifluoracetat; 2-[(-benzothiazole-2- yl)carbonyl]-1-N-[{(L)-Alanyl}-Glycyl]-(2S)-pyrrolidine trifluoracetat; 2-[(pyridin-2- yl)carbonyl]-1-N-[N-{(L)-Alanyl}-(L)-Valinyl]-(2S)-pyrrolidine trifluoracetat,
(3) Substituted aminoketone compounds as disclosed in WO 03/040174, e.g. 1- cyclopentyl-3-methyl-1-oxo-2-pentanaminium chloride, 7-cyclopentyl-3-methyl-1 - oxo-2-butanaminium chloride, 1-cyclopentyl-3,3-dimethyl-1-oxo-2-butanaminium chloride, 1-cyclohexyl-3,3-dimethyl-1-oxo-2-butanaminium chloride, 3- (cyclopentylcarbonyl)-1 ,2,3,4-tetrahydroisoquinolinium chloride, and N-(2- cyclopentyl-2-oxoethyl)cyclohexanaminium chloride,
(4) Side-chain modified DP IV-inhibitors as disclosed in WO 01/14318, and
(5) Prodrugs of DP IV-inhibitors, as disclosed in WO 99/67278 and WO 99/67279.
For the avoidance of doubt, the examples disclosed in each of the above mentioned publications under (1) to (5) are specifically incorporated herein by reference in their entirety, as individually disclosed compounds, especially concerning their structure, their definition, uses and their production.
Pharmaceutical compositions
To prepare the pharmaceutical compositions of this invention, at least one effector of QC optionally in combination with at least one PEP-inhibitor and/or at least one DP IV- inhibitor and/or at least one NPY-receptor-ligand and/or at least one ACE-inhibitor, can be used as the active ingredient(s). The active ingredient(s) is intimately admixed with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques, which carrier may take a wide variety of forms depending of the form of preparation desired for administration, e.g., oral or parenteral such as intramuscular. In preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed. Thus, for liquid oral preparations, such as for example, suspensions, elixirs and solutions, suitable carriers and additives include water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents and the like; for solid oral preparations such as, for example, powders, capsules, gelcaps and tablets, suitable carriers and additives include starches, sugars, diluents, granulating agents, lubricants, binders, disintegrating agents and the like. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit form, in which case solid pharmaceutical carriers are obviously employed. If desired, tablets may be sugar coated or enteric coated by standard techniques. For parenterals, the carrier will usually comprise sterile water, through other ingredients, for example, for purposes such as aiding solubility or for preservation, may be included.
Injectable suspensions may also prepared, in which case appropriate liquid carriers, suspending agents and the like may be employed. The pharmaceutical compositions herein will contain, per dosage unit, e.g., tablet, capsule, powder, injection, teaspoonful and the like, an amount of the active ingredient(s) necessary to deliver an effective dose as described above. The pharmaceutical compositions herein will contain, per dosage unit, e.g., tablet, capsule, powder, injection, suppository, teaspoonful and the like, from about 0.03 mg to 100 mg/kg (preferred 0.1 - 30 mg/kg) and may be given at a dosage of from about 0.1 - 300 mg/kg per day (preferred 1 - 50 mg/kg per day) of each active ingredient or combination thereof. The dosages, however, may be varied depending upon the requirement of the patients, the severity of the condition being treated and the compound being employed. The use of either daily administration or post-periodic dosing may be employed.
Preferably these compositions are in unit dosage forms from such as tablets, pills, capsules, powders, granules, sterile parenteral solutions or suspensions, metered aerosol or liquid sprays, drops, ampoules, autoinjector devices or suppositories; for oral parenteral, intranasal, sublingual or rectal administration, or for administration by inhalation or insufflation. Alternatively, the composition may be presented in a form suitable for once-weekly or once-monthly administration; for example, an insoluble salt of the active compound, such as the decanoate salt, may be adapted to provide a depot preparation for intramuscular injection. For preparing solid compositions such as tablets, the principal active ingredient is mixed with a pharmaceutical carrier, e.g. conventional tableting ingredients such as corn starch, lactose, sucrose, sorbitol, talc, stearic acid, magnesium stearate, dicalcium phosphate or gums, and other pharmaceutical diluents, e.g. water, to form a solid preformulation composition containing a homogeneous mixture of a compound of the present invention, or a pharmaceutically acceptable salt thereof. When referring to these preformulation compositions as homogeneous, it is meant that the active ingredient is dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective dosage forms such as tablets, pills and capsules. This solid preformulation composftion is then subdivided into unit dosage forms of the type described above containing from 0.1 to about 500 mg of each active ingredient or combinations thereof of the present invention.
The tablets or pills of the compositions of the present invention can be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action. For example, the tablet or pill can comprise an inner dosage and an outer dosage component, the latter being in the form of an envelope over the former. The two components can be separated by an enteric layer which serves to resist disintegration in the stomach and permits the inner component to pass intact into the duodenum or to be delayed in release. A variety of material can be used for such enteric layers or coatings, such materials including a number of polymeric acids with such materials as shellac, cetyl alcohol and cellulose acetate.
This liquid forms in which the compositions of the present invention may be incorporated for administration orally or by injection include, aqueous solutions, suitably flavoured syrups, aqueous or oil suspensions, and flavoured emulsions with edible oils such as cottonseed oil, sesame oil, coconut oil or peanut oil, as well as elixirs and similar pharmaceutical vehicles. Suitable dispersing or suspending agents for aqueous suspensions, include synthetic and natural gums such as tragacanth, acacia, alginate, dextran, sodium carboxymethylcellulose, methylcellulose, polyvinylpyrrolidone or gelatin.
Where the processes for the preparation of the compounds of the present invention give rise to mixture of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. The compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution. The compounds may, for example, be resolved into their components enantiomers by standard techniques, such as the formation of diastereomeric pairs by salt formation with an optically active acid, such as (-)-di-p- toluoyl-d-tartaric acid and/or (+)-di-p-toluoyl-!-tartaric acid followed by fractional crystallization and regeneration of the free base. The compounds may also resolved by formation of diastereomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary. Alternatively, the compounds may be resolved using a chiral HPLC column.
During any of the processes for preparation of the compounds of the present invention, it may be necessary and/or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W. McOmie, Plenum Press, 1973; and T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991. The protecting groups may be removed at a convenient subsequent stage using conventional methods known from the art.
The method of treating neuronal disorders as described in the present invention, may also be carried out using a pharmaceutical composition at least one effector of QC optionally in combination with at least one PEP-inhibitor and/or at least one DP IV- inhibitor and/or at least one NPY-receptor-ligand and/or at least one ACE-inhibitor or any other of the compounds as defined herein and a pharmaceutically acceptable carrier. The pharmaceutical composition may contain between about 0.01 mg and 100 mg, preferably about 5 to 50 mg, of each compound, and may be constituted into any form suitable for the mode of administration selected. Carriers include necessary and inert pharmaceutical excipients, including, but not limited to, binders, suspending agents, lubricants, flavorants, sweeteners, preservatives, dyes, and coatings. Compositions suitable for oral administration include solid forms, such as pills, tablets, caplets, capsules (each including immediate release, timed release and sustained release formulations), granules, and powders, and liquid forms, such as solutions, syrups, elixirs, emulsions, and suspensions. Forms useful for parenteral administration include sterile solutions, emulsions and suspensions. Advantageously, compounds of the present invention may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three or four times daily. Furthermore, compounds for the present invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal skin patches well known to those of ordinary skill in that art. To be administered in the form of transdermal delivery system, the dosage administration will, of course, be continuous rather than intermittent throughout the dosage regimen.
For instance, for oral administration in the form of a tablet or capsule, the active drug component can be combined with an oral, non-toxic pharmaceutically acceptable inert carrier such as ethanol, glycerol, water and the like. Moreover, when desired or necessary, suitable binders; lubricants, disintegrating agents and coloring agents can also be incorporated into the mixture. Suitable binders include, without limitation, starch, gelatin, natural sugars such as glucose or betalactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth or sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride and the like. Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum and the like.
The liquid forms in suitable flavored suspending or dispersing agents such as the synthetic and natural gums, for example, tragacanth, acacia, methyl-cellulose and the like. For parenteral administration, sterile suspensions and solutions are desired. Isotonic preparations which generally contain suitable preservatives are employed when intravenous administration is desired.
The compounds or combinations of the present invention can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles. Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine or phosphatidylcholines.
Compounds or combinations of the present invention may also be delivered by the use of monoclonal antibodies as individual carriers to which the compound molecules are coupled. The compounds of the present invention may also be coupled with soluble polymers as targetable drug carriers. Such polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamidephenol, polyhydroxyethylaspartamid-ephenol, or polyethyl eneoxidepolyllysine substituted with palmitoyl residue. Furthermore, the compounds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polyactic acid, polyepsilon caprolactone, polyhydroxy butyeric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and cross-linked or amphipathic block copolymers of hydrogels.
Compounds or combinations of this invention may be administered in any of the foregoing compositions and according to dosage regimens established in the art whenever treatment of the addressed disorders is required.
The daily dosage of the products may be varied over a wide range from 0.01 to 1.000 mg per mammal per day. For oral administration, the compositions are preferably provided in the form of tablets containing, 0.01 , 0.05, 0.1 , 0.5, 1.0, 2.5, 5.0, 10.0, 15.0, 25.0, 50.0, 100, 150, 200, 250 and 500 milligrams of each active ingredient or combinations thereof for the symptomatic adjustment of the dosage to the patient to be treated. An effective amount of the drug is ordinarily supplied at a dosage level of from about 0.1 mg/kg to about 300 mg/kg of body weight per day. Preferably, the range is from about 1 to about 50 mg/kg of body weight per day. The compounds or combinations may be administered on a regimen of 1 to 4 times per day.
Optimal dosages to be administered may be readily determined by those skilled in the art, and will vary with the particular compound used, the mode of administration, the strength of the preparation, the mode of administration, and the advancement of disease condition. In addition, factors associated with the particular patient being treated, including patient age, weight, diet and time of administration, will result in the need to adjust dosages.
Suitably, the particularly beneficial effect provided by the treatment of the invention is an improved therapeutic ratio for the combination of the invention relative to the therapeutic ratio for one compound of the combination when used alone and at a dose providing an equivalent efficacy to the combination of the invention.
In a preferred aspect, the particularly beneficial effect provided by the treatment of the invention is indicated to be a synergistic effect relative to the control expected from the effects of the individual active agents.
In a further aspect of the invention, combining doses of at least one QC-inhibitor with at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY- receptor-ligand will produce a greater beneficial effect than can be achieved for either agent alone at a dose twice that used for that agent in the combination.
In a preferred aspect, the dosage level of each of the active agents when used in accordance with the treatment of the invention will be less than would have been required from a purely additive effect upon the neuronal condition.
It is also considered that the treatment of the invention will effect an improvement, relative to the individual agents, in decreasing the intracellular deposition of pGlu- amyloid-β-peptides and thereby dramatically slowing down the plaque formation in the brain of a mammal, preferably in human brain.
In a further aspect, the invention also provides a process for preparing a pharmaceutical composition comprising at least one at least one effector of QC optionally in combination with at least one PEP-inhibitor and/or at least one DP IV-inhibitor and/or at least one NPY-receptor-ligand and/or at least one ACE-inhibitor and a pharmaceutically acceptable carrier therefor, which process comprises admixing the QC effector and/or DP IV-inhibitor and/or the PEP-inhibitor and/or the NPY-receptor-ligand and/or the ACE- inhibitor and a pharmaceutically acceptable carrier.
The compositions are preferably in a unit dosage form in an amount appropriate for the relevant daily dosage. Suitable dosages, including especially unit dosages, of the QC-inhibitor, the PEP- inhibitor, the DP IV-inhibitor and the NPY-receptor-ligand include the known dosages including unit doses for these compounds as described or referred to in reference text such as the British and US Pharmacopoeias, Remington's Pharmaceutical Sciences (Mack Publishing Co.), Martindale The Extra Pharmacopoeia (London, The Pharmaceutical Press) (for example see the 31st Edition page 341 and pages cited therein) or the above mentioned publications.
Examples of the invention
Figure imgf000058_0001
Example R ESI- S (M+H) Ki (μM)
1 CH3 199.29 13
2 CH(CH3) 241.37 14.7
Figure imgf000058_0002
3 CeH5 261.36 4.4
4 p F-p enyl 279.35 4.73
5 p Cl-p enyl 295.80 1.2
6 p ethyl-phenyl 289.41 2.78 p (triflourmethyl)- 329.4
7 3.93 phenyl p (methoxy-carbonyl) 319.4
8 1.19 -phenyl p (methyl-carbonyl) 303.40
9 1.79 -phenyl
10 p (methoxy)-phenyl 291.40 0.70
Figure imgf000059_0001
t-OI-
Ki
Example R1 R2 R3 R4 X Y MS (μM) (M+H)
11 H OMe H H s NH 291.4 0.700 12 OMe H H H s NH 291.40 1.86 14 H OMe H OMe s NH 321.41 0.565 15 OMe H OMe H s NH 321.41 0.751 16 H OMe OMe H s NH 321.41 0.088 17 OMe OMe OMe H s NH 351.40 0.34 18 H O-CH l2-0 H s NH 305.4 5.66 19 H 0-CH2-CH2-0 H s NH 319.4 1.12 20 H OEt H H s NH 305.4 0.89 21 H SMe H H s NH 307.5 1.66 22 H OMe OMe H 0 NH 305.4 0.461 23 H OMe OMe H s CH2 320.4 0.387
Figure imgf000060_0001
ESI-
Ki
Example R1 R2 R3 MS (μM)
(M+H)
24 H H H 260.3 25 H Me H 274.4 26 H H Me 274.4 27 OMe -(CH2)2- 316.4 2.22 28 Cl -(CH2)3- 334.9 29 Cl -(CH2)4- 348.9 30 OMe -(CH2)5- 358.5 0.425
Figure imgf000060_0002
ESI-MS
Example Ki (μM) (M+H)
31 Me 207.30 1.5
32 p methyl-phenyl 283.3 1.34
33 phenyl 269.3 1.02
34 p-methoxy-phenyl 299.3 0.71
35 3,4-dimethoxyphenyl 329.4 1.36
Figure imgf000061_0001
ESI-MS
Example Ki (μM) (M+H)
36 1 307.4 17.66
37 3 335.4 0.55
Figure imgf000061_0002
ESI-MS
Example position Ki (μM) (M+H)
38 para 383.5 1.86 39 ortho 383.5 40 meta 383.5 3.52
Synthesis of the examples
Figure imgf000062_0001
Synthesis scheme 1: synthesis of the examples 1-22, 36, 37
Reagents and conditions: (a) NaH, DMF, 4h, rt.; (b) ?-?, 8h, 100°C; (c) H2N-NH2l EtOH, 8h, reflux then 4N HCl, 6h, reflux, (d) R-NCO, EtOH, 6h, reflux, (e) R-NCS, 6h, reflux
Figure imgf000062_0002
Synthesis scheme 2: synthesis of the examples 23-30
Reagents and conditions: (a) 1H-imidazole-1-propanamine, CH2CI2, rt., 1h; (b) Laweson's Reaent, EtOH, reflux, 8h
Figure imgf000062_0003
Synthesis scheme 3: synthesis of the examples 31-35 Reagents and conditions: (a) Mel, CH2CI2, rt.,1h; (b) H2N-CN, BuOH, reflux, 8h
Figure imgf000063_0001
Synthesis scheme 4: synthesis of the examples 38-40 Reagents and conditions: (a) NaH, DMF, rt.,3h; (b) LiAIH4, dioxane, reflux, 1 h; (c) R-NCS, EtOH, reflux 6h,
Example 1 - 21
1/-/-imidazole-1-propanamine was reacted with the corresponding isothiocyanate in ethanol under reflux for 8h. After that the solvent was removed and the remaining oil was desolved in methylene chloride. The organic layer was washed twice with a saturated solution of NaHC03 followed by NaHS04 and brine, dried then evaporated. The remaining solid was recrystallised from ethyl acetate, yielding the example thiourea in yields of 80-98%.
Example 22
1/-/-imidazole-1-propanamine was reacted with the corresponding 2,3-dimethoxy- isocyanate in ethanol under reflux for 8h. After that the solvent was removed and the remaining oil was desolved in methylene chloride. The organic layer was washed twice with a saturated solution of NaHC03 followed by NaHS0 and brine, dried then evaporated. The remaining solid was recrystallised from ethyl acetate, giving 22 with yields of 85%.
Example 23-30
1/-/-imidazole-1-propanamine was reacted with the corresponding 2-phenyl acetyl chloride in methylene chloride adding one equivalent of triethylamine. After 2h the solvent was removed and the remaining oil was dissolved in dioxane adding Laweson's Reagent. After stirring for 1.5h a saturated solution of NaHC03 was added. Dioxane was evaporated and the aqueous layer was extrcated by means of ethyl acetate. The organic layer was separated, dried and the solvent was evaporated. The remainig solid was crystallized from acetyl acetate/ether, giving 23-30 with total yields of 62 - 85%.
Example 31-35
All examples were made from the corresponding thioureas by reacting with Mel yielding the thiouronium salts. These intermediates were dissolved in butanole and cyanamide was added. After heating under reflux for 8h butanole was removed and to the remaining oil 0.1M HCl was added. The aqueous layer was extracted by means of methylene chloride. After phase separation the aqueous layer was brought to pH10 and again extracted by means of methylene chloride. Then the organic layer was dried and evaporated giving 31-35 with yields from 40 - 87%.
Example 36,37
The 1/-/-imidazole-1-alkylamines were prepared according to the literature from ω-brom- alkyl-phtalimides and imidazolium salt and. subsequent hydrazinolysis. The resulting products were transformed into the thioureas according to example 1-21 giving a 88% (example 36) and 95% (example 37) yield.
Example 38-40
Imidazole was reacted with the corresponding brommethylphenylcyanide in DMF, utilizing 1 equivalent of NaH for 3h under rt., giving the 1H-imidazole-1- methylphenylcyanides. The solvent was removed and the resulting oil was redissolved in dioxane. The cyanides were converted in the corresponding amines using 1 equivalent of LiAIH . After adding a saturated solution of KHS04, dioxane was evaporated and the aqueous layer was extracted by means of CHCI3. The organic layer was concentrated in vacuo and the amine was converted in the corresponding thioureas according to example 1-21 giving a 78% (example 38) and 65% (example 39) and 81% (example 39) yield. Solid-phase synthesis of peptides
The peptides used herein were synthesized with an automated synthesizer SYMPHONY (RAININ) using a modified Fmoc-protocol. Cycles were modified by using double couplings from the 15th amino acid from the C-terminus of the peptide with fivefold excess of Fmoc-amino acids and coupling reagent. The peptide couplings were performed by TBTU/NMM-activation using a 0.23 mmol substituted NovaSyn TGR-resin or the corresponding preloaded Wang-resin at 25 μmol scale. The cleavage from the resin was carried out by a cleavage-cocktail consisting of 94.5 % TFA, 2.5 % water, 2.5 % EDT and 1 % TIS.
Analytical and preparative HPLC were performed by using different gradients on the LiChrograph HPLC system of Merck-Hitachi. The gradients were made up from two solvents: (A) 0.1 % TFA in H20 and (B) 0.1 % TFA in acetonitrile. Analytical HPLC were performed under the following conditions: solvents were run (1 ml/min) through a 125-4 Nucleosil RP18-column, over a gradient from 5 %-50 % B over 15 min and then up to 95 % B until 20 min, with UV detection (λ = 220 nm). Purification of the peptides was carried out by preparative HPLC on either a 250-20 Nucleosil 100 RP8-column or a 250-10 LiChrospher 300 RP18-column (flow rate 6 ml/min, 220 nm) under various conditions depending on peptide chain length.
For the identification of the peptides and peptide analogues, laser desorption mass spectrometry was employed using the HP G2025 MALDI-TOF system of Hewlett- Packard.
Biological evaluation
Example 1: Determination of ICβo-values of DP IV-inhibitors
100 μl inhibitor stock solution were mixed with 100 μl buffer (HEPES pH 7.6) and 50 μl substrate (Gly-Pro-pNA, final concentration 0.4 mM) and preincubated at 30°C. Reaction was started by addition of 20 μl purified porcine DP IV. Formation of the product pNA was measured at 405 nm over 10 min using the HTS 7000Plus plate reader (Perkin Elmer) and slopes were calculated. The final inhibitor concentrations ranged between 1 mM and 30 nM. For calculation of IC5o-values GraFit 4.0.13 (Erithacus Software) was used. Example 2: Determination ofKj-values of DP IV-inhibitors
For determination of the Kj-values DP IV activity was measured in the same way as described in example 2 at final substrate concentrations of 0.05, 0.1 , 0.2, and 0.4 mM and further 7 inhibitor concentrations covering the IC50 concentration. Calculations were performed using the GraFit Software.
Example 3: Prolyl endopeptidase (PEP) enzymatic activity assays
The enzymatic activity of PEP was quantified as described recently (Schulz et al., 2002, Modulation of inositol 1 ,4,5-triphosphate concentration by prolyl endopeptidase inhibition. Eur J Biochem 269: 5813-5820). Cellular extracts as described above were incubated in the assay buffer using the fluorogenic substrate Z-Gly-Pro-NHMec (10 μM; Bachem, Heidelberg, Germany) on a spectrofluorimeter SFM 25 (excitation wavelength 380 nm, emission wavelength 460 nm, Kontron, Neufahrn, Germany) equipped with a four-cell changer and controlled by an IBM-compatible personal computer. The data obtained were analyzed with the software FLUCOL (Machleidt et al., 1995).
Example 4: Assays for glutaminyi cyclase activity
Fluorometric assays
All measurements were performed with a BioAssay Reader HTS-7000Plus for microplates (Perkin Elmer) at 30 °C. QC activity was evaluated fluorometrically using H- Gln-/?NA. The samples consisted of 0.2 mM fluorogenic substrate, 0.25 U pyroglutamyl aminopeptidase (Unizyme, Hørsholm, Denmark) in 0.2 M Tris/HCI, pH 8.0 containing 20 mM EDTA and an appropriately diluted aliquot of QC in a final volume of 250 μl. Excitation/emission wavelengths were 320/410 nm. The assay reactions were initiated by addition of glutaminyi cyclase. QC activity was determined from a standard curve of ^-naphthylamine under assay conditions. One unit is defined as the amount of QC catalyzing the formation of 1 μmol pGlu-/5NA from H-Gln-^NA per minute under the described conditions. In a second fluorometric assay, QC was activity was determined using H-Gln-AMC as substrate. Reactions were carried out at 30°C utilizing the NOVOStar reader for microplates (BMG lab-technologies). The samples consisted of varying concentrations of the fluorogenic substrate, 0.1 U pyroglutamyl aminopeptidase (Qiagen) in 0.05 M Tris/HCI, pH 8.0 containing 5 mM EDTA and an appropriately diluted aliquot of QC in a final volume of 250 μl. Excitation/emission wavelengths were 380/460 nm. The assay reactions were initiated by addition of glutaminyi cyclase. QC activity was determined from a standard curve of 7-amino-4-methylcoumarin under assay conditions. The kinetic data were evaluated using GraFit sofware.
Spectrophotometric assay of QC
This novel assay was used to determine the kinetic parameters for most of the QC substrates. QC activity was analyzed spectrophotometrically using a continuous method, that was derived by adapting a previous discontinuous assay (Bateman, R. C. J. 1989 J Neurosci Methods 30, 23-28) utilizing glutamate dehydrogenase as auxiliary enzyme. Samples consisted of the respective QC substrate, 0.3 mM NADH, 14 mM α- Ketoglutaric acid and 30 U/ml glutamate dehydrogenase in a final volume of 250 μl. Reactions were started by addition of QC and persued by monitoring of the decrease in absorbance at 340 nm for 8-15 min.
The initial velocities were evaluated and the enzymatic activity was determined from a standard curve of ammonia under assay conditions. All samples were measured at 30°C, using either the SPECTRAFIuor Plus or the Sunrise (both from TECAN) reader for microplates. Kinetic data was evaluated using GraFit software.
Inhibitor assay
For inhibitor testing, the sample composition was the same as described above, except of the putative inhibitory compound added. For a rapid test of QC-inhibition, samples contained 4 mM of the respective inhibitor and a substrate concentration at 1 KM- For detailed investigations of the inhibition and determination of Kj-values, influence of the inhibitor on the auxiliary enzymes was investigated first. In every case, there was no influence on either enzyme detected, thus enabling the reliable determination of the QC inhibition. The inhibitory constant was evaluated by fitting the set of progress curves to the general equation for competitive inhibition using GraFit software.
Example 5: Characterization of effectors of QC
Imidazole derivatives
Imidazole and benzimidazole derivatives carrying substituents in different positions of the 5-membered ring were tested as inhibitors of QC (Table 3). The constitution of the numbers refers to the imidazole ring. The applied methods are described in example 1.
C-4(5) and C-4,5 derivatives. The compounds carrying substitutions in either in the constitutionally equivalent 4- or 5- position of the imidazole ring or in both positions showed a diminished potency for inhibition of human QC. The only exception, however, comprised N-ω-acetylated histamine that proved to be one of the most potent inhibitory compounds. Small substituents in these positions had only little effect on binding as indicated by the similar inhibition constant of 5-hydroxymethyl-4-methyl-imidazole compared to imidazole. Larger and more bulky groups attached to these sites diminished or abolished binding of the compound by the enzyme. Some of the other substituents tested are known to exert negative inductive or mesomeric effects that are capable to reduce the electron density in the imidazole ring, which also contributes to poorer binding constants. The difference in the Kj-values of L-histidine and histidinamide also indicate some influence of the charge on binding. Evidence for electrostatic repulsion of charged substrates were already shown in the substrate specificity studies, i.e. glutaminamide was readily converted to products by human QC, but no reactivity was observed for free glutamine as substrate.
C-2 derivatives. All derivatives tested inhibited QC more weakly as imidazole. Any substitution bigger than a proton hinders proper QC-binding. Only due to the methyl group in 2-methyl-benzimidazole, the inhibition constant drops about one order of magnitude. A very similar relation was shown by comparison of the Kj-values for benzimidazole and 2-amino-benzimidazole. Additionally, the results indicate that the influence is not related to electronic alterations.
N-1 derivatives. Among the imidazole derivatives tested on inhibition of human QC, most compounds that had improved Kj-values compared to imidazole showed alterations at one nitrogen atom. These compounds also contained one of the most effective QC inhibitors, 1-benzylimidazole. Interestingly, only little alterations of this structure led to a loss of inhibitory quality, as can be seen for 1-benzoylimidazole and phenylimidazole, which was inactive under the experimental conditions. Also in this case, the observed changes seemed not to be only caused by a reduced electron density of the imidazole ring due to the negative mesomeric effect of the Phenyl group, because also the bulky trimethyl-silyl group, exhibiting a positive inductive effect showed reduced binding compared to other residues. Interestingly, one of the less effective compounds of this group was 1-aminopropyl-imidazole. The small efficacy of this compound is caused by the basic amino group, since the sterically similar compounds 1-methylimidazole and 1-vinylimidazole showed improved binding to the active site. Thus, the positively charged amino group accounts for the smaller Kj-value, a result that is corroborated by a comparison of the Kj-values of N-ω-acetylated histamine (Table 3) and histamin (Table 4).
Effect of 3,4 and 3,5 derivatization. The imidazole derivatives that contained substituents in positions 4(5) or both were shown to have a restricted efficiency for binding to the enzyme. The effect of the specific substitutions were specified by comparison of the inhibitory constants of L-histamine and the two intermediates in the biological degradation of histamine, 3-methyl-4-histamine and 3-methyl-5-histamine (Table 4). L-Histamine revealed a K value that was about one order of magnitude smaller compared to its acetylated counterpart. Methylation of one nitrogen resulted in a considerable improvement of efficacy in case of 3-methyl-4-histamine. Methylation leading to 3-methyl-5-histamine, however, resulted in a complete loss of inhibitory activity. Thus, the observed effect seems to be mainly caused by a sterical hindrance of binding due to the derivatisation of the carbon adjacent to the basic nitrogen. Presumably, the basic nitrogen plays a key role for binding to the enzyme. Example 6: MALDI-TOF mass spectrometry
Matrix-assisted laser desorption/ionization mass spectrometry was carried out using the Hewlett-Packard G2025 LD-TOF System with a linear time of flight analyzer. The instrument was equipped with a 337 nm nitrogen laser, a potential acceleration source (5 kV) and a 1.0 m flight tube. Detector operation was in the positive-ion mode and signals were recorded and filtered using LeCroy 9350M digital storage oscilloscope linked to a personal computer. Samples (5 μl) were mixed with equal volumes of the matrix solution. For matrix solution we used DHAP/DAHC, prepared by solving 30 mg 2',6'-dihydroxyacetophenone (Aldrich) and 44 mg diammonium hydrogen citrate (Fluka) in 1 ml acetonitrile/0.1% TFA in water (1/1 , v/v). A small volume (« 1 μl) of the matrix-analyte-mixture was transferred to a probe tip and immediately evaporated in a vacuum chamber (Hewlett-Packard G2024A sample prep accessory) to ensure rapid and homogeneous sample crystallization. For long-term testing of Glu1-cyclization, Aβ-derived peptides were incubated in 100μl 0.1 M sodium acetate buffer, pH 5.2 or 0.1 M Bis-Tris buffer, pH 6.5 at 30°C. Peptides were applied in 0.5 mM [Aβ(3-11)a] or 0.15 mM [Aβ(3-21)a] concentrations, and 0.2 U QC was added all 24 hours. In case of Aβ(3-21)a, the assays contained 1 % DMSO. At different times, samples were removed from the assay tube, peptides extracted using ZipTips (Millipore) according to the manufacturer's recommendations, mixed with matrix solution (1 :1 v/v) and subsequently the mass spectra recorded. Negative controls did either contain no QC or heat deactivated enzyme. For the inhibitor studies the sample composition was the same as described above, with exception of the inhibitory compound added (5 mM benzimidazole or 2 mM 1 ,10-phenanthroline).

Claims

Patent Claims
1. Use of inhibitors of glutaminyi cyclase (QC) for the preparation of a medicament for the treatment and/or prevention of a disease selected from the group consisting of Alzheimer's Disease, Down syndrome and Huntington's Disease in mammals.
2. The use according to claim 1 wherein the QC-inhibitor has the general formula 1 including pharmaceutically acceptable salts thereof, including all stereoisomers and polymorphs:
Figure imgf000071_0001
formula 1 wherein n is 1 , 2, 3 or 4, preferably 2 or 3, especially 2, and A can be a saturated or unsaturated heterocycle and may be substituted or unsubstituted, and wherein Ri is H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri optionally being substituted independently of each other.
3. The use according to claim 1 wherein the QC-inhibitor has the general formula 2 including pharmaceutically acceptable salts thereof, including all stereoisomers and polymorphs:
Figure imgf000071_0002
formula 2 wherein
Ri, R2 and R3 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues R-i, R2 and R3 optionally being substituted independently of each other.
4. The use according to claim 1 wherein the QC-inhibitor has the general formula 2a including pharmaceutically acceptable salts thereof, including all stereoisomers and polymorphs:
N^\
I N-A-B
formula 2a
wherein A is a branched or unbranched C^C/ alkyl chain, a branched or unbranched Cι-C7 alkenyl chain, a branched or unbranched C1-C7 alkynyl chain,
or wherein A is a compound selected from the group consisting of :
Figure imgf000072_0001
wherein R6-R10 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle , preferably H or methyl,
wherein n and n1 are independently 1 - 5, m is 1 - 5 , o is 0 - 4,
wherein B is a compound selected from the group consisting of
Figure imgf000073_0001
(VI) (VII)
Figure imgf000073_0002
wherein D and E are a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, or a heterocycle,
wherein Z is CH or N, wherein X can be O, S or N-CN, with the proviso for formulas (VIII) and (IX) that, if Z = CH, X is O or S,
wherein X1 , X2 and X3 are independently O or S,
wherein Y is O or S,
wherein R11-R14 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, halogenyl, oxyalkyl, thioalkyl, carboxyl, carboxylic acid ester, carbonyl, carbamide, carbimide, thiocarbamide or thiocarbonyl,
wherein R15 and R16 are independently H or a branched or unbranched alkyl chain, or a branched or unbranched alkenyl chain,
wherein R17 and R18 are independently of each other H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl or can be connected to form a carbocycle with up to 6 ring atoms,
wherein n is 0 or 1 ,
all of the above residues being optionally substituted independently of each other.
5. The use according to claim 1 wherein the QC-inhibitor has the general formula 3 including the pharmaceutically acceptable salts thereof, including all stereoisomers and polymorphs:
Figure imgf000074_0001
wherein n is 1 , 2, 3 or 4, preferably 2 or 3, especially 2, and A can be a saturated or unsaturated heterocycle and may be substituted or unsubstituted, and wherein Ri and R2 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza- peptide, peptide or a mimetic thereof; all of the above residues R^ and R2 optionally being substituted independently of each other.
6. The use according to claim 1 wherein the QC-inhibitor has the general formula
4 including pharmaceutically acceptable salts thereof, including all stereoisomers and polymorphs:
Figure imgf000075_0001
formula 4 wherein n is 1 , 2, 3 or 4, preferably 2 or 3, especially 2, and A can be a saturated or unsaturated heterocycle and may be substituted or unsubstituted, and wherein R^ R2 and R3 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza- peptide, peptide or a mimetic thereof; all of the above residues Ri, R2 and R3 optionally being substituted independently of each other.
7. The use according to claim 1 wherein the QC-inhibitor has the general formula
5 including pharmaceutically acceptable salts thereof, including all stereoisomers and polymorphs:
Figure imgf000075_0002
formula 5 wherein Ri, R2, R3, R4 and R5 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues Ri, R2, R3, R and R5 optionally being substituted independently of each other.
8. The use according to claim 1 wherein the QC-inhibitor has the general formula 6 including pharmaceutically acceptable salts thereof, including all stereoisomers and polymorphs:
Figure imgf000076_0001
formula 6 wherein
Ri, R2, R3, R and R5 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, aza-amino acid, amino acid or a mimetic thereof, aza-peptide, peptide or a mimetic thereof; all of the above residues R1 f R2, R3, R and R5 optionally being substituted independently of each other.
9. A compound of the formula 2a including pharmaceutically acceptable salts thereof, including all stereoisomers and polymorphs:
N^\
I N-A-B
formula 2a
wherein A is a branched or unbranched Cι-C7 alkyl chain, a branched or unbranched C1-C7 alkenyl chain, a branched or unbranched Cι-C7 alkynyl chain,
or wherein A is a compound selected from the group consisting of :
Figure imgf000077_0001
(I) (II) (III)
Figure imgf000077_0002
wherein R6-R10 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, preferably H or methyl,
wherein n and n1 are independently 1 - 5, m is 1 - 5 , o is 0 - 4,
wherein B is a compound selected from the group consisting of
Figure imgf000078_0001
(VI) (VII)
Figure imgf000078_0002
(XIV)
wherein D and E are a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl or a heterocycle,
wherein Z is CH or N, wherein X can be O, S or N-CN, with the proviso for formulas (VIII) and (IX) that, if Z = CH, X is O or S,
wherein X1 , X2 and X3 are independently O or S with the proviso for compound (XIV) that at least one of X2 and X3 must be S,
wherein Y is O or S, with the proviso that Y may not be O when the carbocycle formed by R17 and R18 has 3 members in the ring,
wherein R11-R14 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl, heteroaryl, a heterocycle, halogenyl, oxyalkyl, thioalkyl, carboxyl, carboxylic acid ester, carbonyl, carbamide, carbimide, thiocarbamide or thiocarbonyl,
wherein R15 and R16 are independently H or a branched or unbranched alkyl chain, or a branched or unbranched alkenyl chain,
wherein R17 and R18 are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, aryl or can be connected to form a carbocycle with up to 6 ring atoms, and
wherein n is 0 or 1 ,
all of the above residues being optionally substituted independently of each other.
10. The compound according to claim 9, wherein A is a C3 alkyl chain, a C3 methyl branched alkyl chain, cycloalkyl- 1 ,1 -dimethyl of formula (IV) with m = 1-4, 1 ,4- dimethylphenyl or 1 ,3-dimethylphenyl.
11. The compound according to claims 9 or 10, wherein D and E are a substituted phenyl, wherein substitution means oxyalkyl, thioalkyl, halogenyl, carboxylic acid alkyl ester or aryl ester.
12. The compound according to claims 9 or 10, wherein D and E are dihydrobenzodioxine, benzodioxole, benzodithiole, dihydrobenzodithiine, benzooxathiole or dihydrobenzooxathiine.
13. The compound according to any one of claims 9 to 12, wherein X is S.
14. The compound according to any one of claims 9 to 13, wherein Z is N.
15. The compound according to any one of claims 9 to 14, wherein R1 and R 4 are H.
16. The compound according to any one of claims 9 to 15, wherein R12 and R13 are independently oxyalkyl or thioalkyl, halogenyl, or carboxylic acid alkylester, or R12 and R13 are connected to form a dihydrobenzodioxine, a benzodioxole, a benzodithiole, a dihydrobenzodithiine, a benzooxathiole, a dihydrobenzooxathiine.
17. The compound according to any one of claims 9 to 16, wherein at least one of R15 and R16 is H.
18. The compound according to any one of claims 9 to 17, wherein R15 and R16 are both H.
19. The compound according to any one of claims 9 to 12, wherein B has the formula
Figure imgf000080_0001
(VII)
20. The compound according to claim 19, wherein R17 and R δ are independently H or a branched or unbranched alkyl chain, a branched or unbranched alkenyl chain, a branched or unbranched alkynyl chain, a carbocycle, or aryl.
21. The compound of claim 19 or 20, wherein one of R and R is H and the other is Me.
22. The compound of claim 19 or 20, wherein one of R17 and R18 is H and the other is phenyl.
23. The compound of claim 19 or 20, wherein R17 and R18 form a carbocycle with up to 6 ring atoms.
24. The compound according to any one of the claims 9 to 23 for the use as apharmaceutical.
25. A pharmaceutical composition for parenteral, enteral or oral administration, comprising at least one compound according to any one of the claims 9 to 24 optionally in combination with a therapeutically acceptable carrier and/or excipient.
26. The pharmaceutical composition of claim 25, which comprises additionally at least one agent, selected from the group consisting of PEP-inhibitors, inhibitors of DP IV/DP IV-like enzymes, NPY-receptor ligands, NPY agonists, NPY antagonists and ACE inhibitors and a pharmaceutically acceptable carrier therefore, for use as an active therapeutic substance.
27. The pharmaceutical composition according to claim 26, wherein said inhibitor of DP IV/DP IV-like enzymes is selected from the group consisting of L-threo-isoleucyl pyrrolidide, L-allo-isoleucyl thiazolidide, L-allo-isoleucyl pyrrolidide; and salts thereof or valine pyrrolidide, NVP-DPP728A (1-[ [ [ 2-[ {5-cyanopyridin-2- yl}amino]ethyl]amino]acetyl]-2-cyano-(S)-pyrrolidine) LAF-237 (1 -[(3-hydroxy- adamant-1-ylamino)-acetyl]-pyrrolidine-2(S)-carbonitrile); TSL-225 (tryptophyl- 1 ,2,3,4-tetrahydroisoquinoline-3-carboxylic acid), FE-999011 ( [(2S)-1-([2'S]-2'- amino-3',3'dimethyl-butanoyl)-pyrrolidine-2-carbonitrile] ), GW-229A, 815541 , MK- 431 or PT-100 (Point Therapeutics).
28. The pharmaceutical composition according to claim 26, wherein said inhibitor of DP IV/DP IV-like enzymes is selected from glutaminyi pyrrolidine and glutaminyi thiazolidine of formulas (8) and (9), or a pharmaceutically acceptable salt thereof, preferably the hydrochloric salt:
Figure imgf000082_0001
(8)
Figure imgf000082_0002
(9)
29. The pharmaceutical composition according to any one of the claims 26 to 28, wherein said NPY antagonist is selected from 3a,4,5,9b-tetrahydro-1h-benz[e]indol-2- yl amine, BIBP3226 and, (R)-N2-(diphenylacetyl)-(R)-N-[1-(4-hydroxy- phenyl) ethyl] arginine amide.
30. The pharmaceutical composition according to any one of the claims 26 to 29, wherein said PEP-inhibitor is selected from the group consisting of chemical derivatives of proline or small peptides containing terminal prolines, e.g. benzyloxycarbonyl-prolyl-prolinal, N-terminal substituted L-proline or L- prolylpyrrolidine, substituted N-benzyloxycarbonyl (Z) dipeptides containing prolinal at the carboxy terminus, substituted thioprolines, substituted thiazolidines, substituted oxopyrrolidines, carboxy terminal modified prolines including fluorinated ketone derivatives, chloromethyl ketone derivatives of acyl-proline or acylpeptide-proline (Z- Gly-Pro-CHaCI) and 2-acylpyrrolidine derivatives.
31. The pharmaceutical composition according to any one of the claims 26 to 29, wherein said PEP-inhibitor is selected from the group consisting of Fmoc-Ala-Pyrr- CN, Z-321 , ONO-1603, JTP-4819 and S-17092.
32. The pharmaceutical composition according to any one of the claims 26 to 31 , wherein said ACE-inhibitor is SDZ ENA 713 (rivastigmine (+)-(S)-N-ethyl-3-[(1- dimethylamino)ethyl]-N-methylphenylcarbamate hydrogen tartrate.
33. The use of the pharmaceutical composition according to any of the claims 25 to 32, for the treatment of neuronal disorders, especially Alzheimer's disease, Down Syndrome, Parkinson disease, Chorea Huntington, pathogenic psychotic conditions, schizophrenia, impaired food intake, sleep-wakefulness, impaired homeostatic regulation of energy metabolism, impaired autonomic function, impaired hormonal balance, impaired regulation, body fluids, hypertension, fever, sleep dysregulation, anorexia, anxiety related disorders including depression, seizures including epilepsy, drug withdrawal and alcoholism, neurodegenerative disorders including cognitive dysfunction and dementia.
34. The use of the pharmaceutical composition according to any one of the claims 25 to 33 for the treatment of a neuronal disease, selected from the group consisting of Alzheimer's disease, Down Syndrome, Parkinson disease and Chorea Huntington.
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