DE502004009527D1 - Arzneimittel enthaltend substituierte 2-heteroaryl-aminoessigsäure-verbindungen - Google Patents
Arzneimittel enthaltend substituierte 2-heteroaryl-aminoessigsäure-verbindungenInfo
- Publication number
- DE502004009527D1 DE502004009527D1 DE502004009527T DE502004009527T DE502004009527D1 DE 502004009527 D1 DE502004009527 D1 DE 502004009527D1 DE 502004009527 T DE502004009527 T DE 502004009527T DE 502004009527 T DE502004009527 T DE 502004009527T DE 502004009527 D1 DE502004009527 D1 DE 502004009527D1
- Authority
- DE
- Germany
- Prior art keywords
- optionally substituted
- heteroaryl
- specifically
- aryl
- mono
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000002253 acid Substances 0.000 title abstract 3
- -1 AMINO Chemical class 0.000 title 1
- 230000002378 acidificating effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 229940079593 drug Drugs 0.000 title 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 2
- HOKKHZGPKSLGJE-GSVOUGTGSA-N N-Methyl-D-aspartic acid Chemical compound CN[C@@H](C(O)=O)CC(O)=O HOKKHZGPKSLGJE-GSVOUGTGSA-N 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 230000000202 analgesic effect Effects 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 150000004677 hydrates Chemical class 0.000 abstract 2
- 150000003840 hydrochlorides Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 159000000000 sodium salts Chemical class 0.000 abstract 2
- 239000012453 solvate Substances 0.000 abstract 2
- 239000004471 Glycine Substances 0.000 abstract 1
- 241000699670 Mus sp. Species 0.000 abstract 1
- 108090001041 N-Methyl-D-Aspartate Receptors Proteins 0.000 abstract 1
- 230000000954 anitussive effect Effects 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 230000002075 anti-alcohol Effects 0.000 abstract 1
- 230000003266 anti-allergic effect Effects 0.000 abstract 1
- 230000001773 anti-convulsant effect Effects 0.000 abstract 1
- 230000001430 anti-depressive effect Effects 0.000 abstract 1
- 230000003178 anti-diabetic effect Effects 0.000 abstract 1
- 230000036436 anti-hiv Effects 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 230000000648 anti-parkinson Effects 0.000 abstract 1
- 230000001139 anti-pruritic effect Effects 0.000 abstract 1
- 239000001961 anticonvulsive agent Substances 0.000 abstract 1
- 239000000935 antidepressant agent Substances 0.000 abstract 1
- 229940005513 antidepressants Drugs 0.000 abstract 1
- 239000003472 antidiabetic agent Substances 0.000 abstract 1
- 229960003965 antiepileptics Drugs 0.000 abstract 1
- 239000000939 antiparkinson agent Substances 0.000 abstract 1
- 239000003908 antipruritic agent Substances 0.000 abstract 1
- 229940124584 antitussives Drugs 0.000 abstract 1
- 230000001966 cerebroprotective effect Effects 0.000 abstract 1
- PCHPORCSPXIHLZ-UHFFFAOYSA-N diphenhydramine hydrochloride Chemical compound [Cl-].C=1C=CC=CC=1C(OCC[NH+](C)C)C1=CC=CC=C1 PCHPORCSPXIHLZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000010534 mechanism of action Effects 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 239000003176 neuroleptic agent Substances 0.000 abstract 1
- 230000000701 neuroleptic effect Effects 0.000 abstract 1
- 230000000324 neuroprotective effect Effects 0.000 abstract 1
- 230000001777 nootropic effect Effects 0.000 abstract 1
- 125000003367 polycyclic group Chemical group 0.000 abstract 1
- 238000000159 protein binding assay Methods 0.000 abstract 1
- 230000020341 sensory perception of pain Effects 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
- 229940125725 tranquilizer Drugs 0.000 abstract 1
- 239000003204 tranquilizing agent Substances 0.000 abstract 1
- 230000002936 tranquilizing effect Effects 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10306203A DE10306203A1 (de) | 2003-02-13 | 2003-02-13 | Arzneimittel enthaltend substituierte 2-Heteroaryl-Aminoessigsäure-Verbindungen |
PCT/EP2004/001061 WO2004071380A2 (de) | 2003-02-13 | 2004-02-05 | Arzneimittel enthaltend substituierte 2-heteroaryl-aminoessigsäure-verbindungen |
Publications (1)
Publication Number | Publication Date |
---|---|
DE502004009527D1 true DE502004009527D1 (de) | 2009-07-09 |
Family
ID=32747842
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE10306203A Withdrawn DE10306203A1 (de) | 2003-02-13 | 2003-02-13 | Arzneimittel enthaltend substituierte 2-Heteroaryl-Aminoessigsäure-Verbindungen |
DE502004009527T Expired - Lifetime DE502004009527D1 (de) | 2003-02-13 | 2004-02-05 | Arzneimittel enthaltend substituierte 2-heteroaryl-aminoessigsäure-verbindungen |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE10306203A Withdrawn DE10306203A1 (de) | 2003-02-13 | 2003-02-13 | Arzneimittel enthaltend substituierte 2-Heteroaryl-Aminoessigsäure-Verbindungen |
Country Status (6)
Country | Link |
---|---|
US (1) | US7754754B2 (de) |
EP (1) | EP1596852B1 (de) |
AT (1) | ATE432073T1 (de) |
DE (2) | DE10306203A1 (de) |
ES (1) | ES2327843T3 (de) |
WO (1) | WO2004071380A2 (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010139481A1 (en) * | 2009-06-04 | 2010-12-09 | Merz Pharma Gmbh & Co. Kgaa | Glycine b antagonists |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9027210D0 (en) * | 1990-12-14 | 1991-02-06 | Smithkline Beecham Plc | Medicaments |
GB9426078D0 (en) * | 1994-12-23 | 1995-02-22 | Cadbury Schweppes Plc | Process for manufacture of reduced fat chocolate |
DE19549825B4 (de) * | 1995-09-02 | 2010-11-04 | Südzucker AG Mannheim/Ochsenfurt | Zuckerfreie Hartkaramellen |
JP2000514797A (ja) * | 1996-06-28 | 2000-11-07 | ユニバーシティ オブ サザン カリフォルニア | 有機ホウ素誘導体を用いるアミンおよびアミノ酸の合成方法 |
US6602817B1 (en) | 1998-10-23 | 2003-08-05 | University Of Southern California | Combination approach to chiral reagents or catalysts having amine or amino alcohol ligands |
US6096782A (en) * | 1996-11-22 | 2000-08-01 | Athena Neurosciences, Inc. | N-(aryl/heteroaryl) amino acid derivatives pharmaceutical compositions comprising same and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds |
TR199902826T2 (xx) * | 1997-04-18 | 2000-02-21 | Mcneil-Ppc,Inc. | D���k kalorili, lezzetli fiber-i�eren, �eker muadili |
US5952205A (en) * | 1998-02-06 | 1999-09-14 | Neose Technologies, Inc. | Process for processing sucrose into glucose and fructose |
AU2001234560A1 (en) * | 2000-01-25 | 2001-08-07 | The Procter And Gamble Company | Solid-supported process for making n-substituted peptide mimetic compounds |
US6783790B1 (en) * | 2000-05-19 | 2004-08-31 | Hershey Foods Corporation | Process utilizing agar-agar in a high temperature, short time processing of high solids confectionery products |
DE10059864A1 (de) * | 2000-11-30 | 2002-06-13 | Gruenenthal Gmbh | Substituierte Amino-furan-2-yl-essigsäure- und Amino-thien-2-yl-essigsäure-Derivate |
-
2003
- 2003-02-13 DE DE10306203A patent/DE10306203A1/de not_active Withdrawn
-
2004
- 2004-02-05 WO PCT/EP2004/001061 patent/WO2004071380A2/de active Application Filing
- 2004-02-05 ES ES04708322T patent/ES2327843T3/es not_active Expired - Lifetime
- 2004-02-05 EP EP04708322A patent/EP1596852B1/de not_active Expired - Lifetime
- 2004-02-05 DE DE502004009527T patent/DE502004009527D1/de not_active Expired - Lifetime
- 2004-02-05 AT AT04708322T patent/ATE432073T1/de active
-
2005
- 2005-08-12 US US11/202,074 patent/US7754754B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
DE10306203A1 (de) | 2004-08-26 |
ATE432073T1 (de) | 2009-06-15 |
EP1596852B1 (de) | 2009-05-27 |
WO2004071380A2 (de) | 2004-08-26 |
US7754754B2 (en) | 2010-07-13 |
EP1596852A2 (de) | 2005-11-23 |
WO2004071380A3 (de) | 2005-01-06 |
US20060025473A1 (en) | 2006-02-02 |
ES2327843T3 (es) | 2009-11-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8364 | No opposition during term of opposition | ||
R082 | Change of representative |
Ref document number: 1596852 Country of ref document: EP Representative=s name: , |