WO2007047978A3 - Modulation of neurogenesis by pde inhibition - Google Patents

Modulation of neurogenesis by pde inhibition Download PDF

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Publication number
WO2007047978A3
WO2007047978A3 PCT/US2006/041131 US2006041131W WO2007047978A3 WO 2007047978 A3 WO2007047978 A3 WO 2007047978A3 US 2006041131 W US2006041131 W US 2006041131W WO 2007047978 A3 WO2007047978 A3 WO 2007047978A3
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WO
WIPO (PCT)
Prior art keywords
neurogenesis
modulation
pde inhibition
pde
stimulate
Prior art date
Application number
PCT/US2006/041131
Other languages
French (fr)
Other versions
WO2007047978A2 (en
Inventor
Carrolee Barlow
Todd A Carter
Kym I Lorrain
Jammieson C Pires
Kai Treuner
Original Assignee
Braincells Inc
Carrolee Barlow
Todd A Carter
Kym I Lorrain
Jammieson C Pires
Kai Treuner
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Braincells Inc, Carrolee Barlow, Todd A Carter, Kym I Lorrain, Jammieson C Pires, Kai Treuner filed Critical Braincells Inc
Priority to JP2008536840A priority Critical patent/JP2009512711A/en
Priority to AU2006304787A priority patent/AU2006304787A1/en
Priority to EP06826395A priority patent/EP1940389A2/en
Priority to CA002625153A priority patent/CA2625153A1/en
Publication of WO2007047978A2 publication Critical patent/WO2007047978A2/en
Publication of WO2007047978A3 publication Critical patent/WO2007047978A3/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/401Proline; Derivatives thereof, e.g. captopril
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4015Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/4161,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41661,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
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    • A61P25/24Antidepressants
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/32Alcohol-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Abstract

The instant disclosure describes methods for treating diseases and conditions of the central and peripheral nervous system by stimulating or increasing neurogenesis. The disclosure includes compositions and methods based on use of a PDE agent, optionally in combination with one or more other neurogenic agents, to stimulate or activate the formation of new nerve cells.
PCT/US2006/041131 2005-10-21 2006-10-20 Modulation of neurogenesis by pde inhibition WO2007047978A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2008536840A JP2009512711A (en) 2005-10-21 2006-10-20 Regulation of neurogenesis by PDE inhibition
AU2006304787A AU2006304787A1 (en) 2005-10-21 2006-10-20 Modulation of neurogenesis by PDE inhibition
EP06826395A EP1940389A2 (en) 2005-10-21 2006-10-20 Modulation of neurogenesis by pde inhibition
CA002625153A CA2625153A1 (en) 2005-10-21 2006-10-20 Modulation of neurogenesis by pde inhibition

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US72936605P 2005-10-21 2005-10-21
US60/729,366 2005-10-21
US78460506P 2006-03-21 2006-03-21
US60/784,605 2006-03-21
US80759406P 2006-07-17 2006-07-17
US60/807,594 2006-07-17

Publications (2)

Publication Number Publication Date
WO2007047978A2 WO2007047978A2 (en) 2007-04-26
WO2007047978A3 true WO2007047978A3 (en) 2007-08-09

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PCT/US2006/041131 WO2007047978A2 (en) 2005-10-21 2006-10-20 Modulation of neurogenesis by pde inhibition

Country Status (6)

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US (1) US7985756B2 (en)
EP (2) EP1940389A2 (en)
JP (1) JP2009512711A (en)
AU (1) AU2006304787A1 (en)
CA (1) CA2625153A1 (en)
WO (1) WO2007047978A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8555875B2 (en) 2008-12-23 2013-10-15 Map Pharmaceuticals, Inc. Inhalation devices and related methods for administration of sedative hypnotic compounds

Families Citing this family (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007008758A2 (en) * 2005-07-08 2007-01-18 Braincells, Inc. Methods for identifying agents and conditions that modulate neurogenesis
US20110275664A1 (en) * 2005-09-26 2011-11-10 The Regents Of The University Of Colorado,A Body Corporate Method for treating drug and behavioral addictions
US7915285B2 (en) * 2005-09-26 2011-03-29 The Regents Of The University Of Colorado Method for treating drug and behavioral addictions
CA2558746A1 (en) * 2005-12-12 2006-12-04 Janssen Pharmaceutica N.V. Use of paliperidone for the treatment of substance abuse
JP2009536667A (en) 2006-05-09 2009-10-15 ブレインセルス,インコーポレイティド 5HT receptor-mediated neurogenesis
JP2009536669A (en) * 2006-05-09 2009-10-15 ブレインセルス,インコーポレイティド Neurogenesis by angiotensin regulation
US7858611B2 (en) 2006-05-09 2010-12-28 Braincells Inc. Neurogenesis by modulating angiotensin
US20090197823A1 (en) * 2006-05-09 2009-08-06 Braincells, Inc. Aliskiren modulation of neurogenesis
WO2007142924A1 (en) 2006-05-31 2007-12-13 Avigen, Inc. Ibudilast for inhibiting macrophage migration inhibitory factor (mif) activity
WO2007143705A2 (en) 2006-06-06 2007-12-13 Intra-Cellular Therapies, Inc. Organic compounds
ES2443342T3 (en) 2006-07-05 2014-02-19 Takeda Gmbh Combination of HMG-CoA reductase rosuvastatin inhibitor with a phosphodiesterase 4 inhibitor, such as roflumilast, roflumilast-N-oxide for the treatment of inflammatory lung diseases
US20080103105A1 (en) * 2006-09-22 2008-05-01 Braincells, Inc. HMG CoA REDUCTASE MEDIATED MODULATION OF NEUROGENESIS
US20080171750A1 (en) * 2007-01-11 2008-07-17 Braincells, Inc. Modulation Of Neurogenesis With Use of Modafinil
US20080188457A1 (en) * 2007-02-02 2008-08-07 Braincells, Inc. Modulation of Neurogenesis with Biguanides and GSK3-beta Agents
US8637528B2 (en) * 2007-03-27 2014-01-28 Omeros Corporation Use of PDE7 inhibitors for the treatment of movement disorders
EP2139475B1 (en) * 2007-03-27 2014-12-17 Omeros Corporation PDE7 inhibitors for use in the treatment of movement disorders
CA2684879A1 (en) * 2007-05-15 2008-11-27 Helicon Therapeutics, Inc. Methods of identifying genes involved in memory formation using small interfering rna (sirna)
DK2187882T3 (en) 2007-07-11 2013-04-08 Medicinova Inc Treatment of progressive neurodegenerative disease with ibudilast
WO2009017625A1 (en) * 2007-07-27 2009-02-05 Avigen, Inc. Treatment of depression, phychosis, and anxiety
WO2009073210A1 (en) * 2007-12-06 2009-06-11 Intra-Cellular Therapies, Inc Organic compounds
WO2009076529A1 (en) 2007-12-11 2009-06-18 Research Development Foundation Small molecules for neuronal differentiation of embryonic stem cells
JP2011507835A (en) 2007-12-21 2011-03-10 アンドレイ・アレクサンドロビッチ・イワシェンコ Alpha-adrenergic receptor, dopamine, histamine, imidazoline and serotonin receptor ligands and uses thereof
PE20120120A1 (en) 2008-12-06 2012-03-03 Intra Cellular Therapies Inc DERIVATIVES OF 2H-PYRAZOLO [3,4-d] PYRIMIDINE-4,6 (5H, 7H) -DIONA, AS PDE1 INHIBITORS
BRPI0922700A2 (en) 2008-12-06 2015-08-11 Intracellular Therapies Inc Organic compounds
ES2580759T3 (en) 2008-12-06 2016-08-26 Intra-Cellular Therapies, Inc. Organic compounds
JP2012513464A (en) * 2008-12-23 2012-06-14 ザ トラスティーズ オブ コロンビア ユニヴァーシティ イン ザ シティ オブ ニューヨーク Phosphodiesterase inhibitors and uses thereof
US8355927B2 (en) 2010-11-05 2013-01-15 Genomind, Llc Neuropsychiatric test reports
WO2011111066A2 (en) * 2010-03-12 2011-09-15 Connexios Life Sciences Pvt. Ltd. Composition and uses thereof
EP2590657A4 (en) 2010-05-31 2014-02-12 Intra Cellular Therapies Inc Organic compounds
US9434730B2 (en) 2010-05-31 2016-09-06 Intra-Cellular Therapies, Inc. PDE1 inhibitor compounds
CN106038567A (en) * 2010-11-08 2016-10-26 奥默罗斯公司 Treatment of addiction and impulse-control disorders using pde7 inhibitors
US9220715B2 (en) * 2010-11-08 2015-12-29 Omeros Corporation Treatment of addiction and impulse-control disorders using PDE7 inhibitors
AU2013201989B2 (en) * 2010-11-08 2016-01-07 Omeros Corporation Treatment of addiction and impulse-control disorders using PDE7 inhibitors
WO2012123406A1 (en) * 2011-03-17 2012-09-20 Algiax Pharmaceuticals Gmbh Novel use of imidazotriazinones
WO2012149535A1 (en) * 2011-04-29 2012-11-01 Genomind, Llc The use of angiotensin ii (at ii) type 1 receptor antagonist in the therapeutic treatment of autism
US20130045988A1 (en) * 2011-08-18 2013-02-21 Shire Ag Combination therapy
EP2751095B1 (en) 2011-08-29 2021-10-27 Sanford-Burnham Medical Research Institute Novel benzodiazepinones as modulators of metabotropic glutamate receptor functions and neurological uses thereof
EP2785183B1 (en) * 2011-11-14 2018-12-19 Merck Sharp & Dohme Corp. Triazolopyridinone pde10 inhibitors
US20140044813A1 (en) * 2012-08-09 2014-02-13 Kemin Industries, Inc. Plant Extracts for Improving Cognitive Health and Function
EP3091983B1 (en) 2014-01-08 2019-10-02 Intra-Cellular Therapies, Inc. Pharmaceutical compositions comprising a pde-1 inhibitor and a pde-2 inhibitor
US9546175B2 (en) 2014-08-07 2017-01-17 Intra-Cellular Therapies, Inc. Organic compounds
EP3226862B1 (en) 2014-12-06 2020-07-08 Intra-Cellular Therapies, Inc. Phosphodiesterase 2 (pde2) inhibitory compounds
EP3226870B1 (en) 2014-12-06 2019-09-25 Intra-Cellular Therapies, Inc. Organic compounds
GB2536650A (en) 2015-03-24 2016-09-28 Augmedics Ltd Method and system for combining video-based and optic-based augmented reality in a near eye display
CN107708446A (en) 2015-06-22 2018-02-16 雀巢产品技术援助有限公司 For strengthening the composition and method of the formation of animal nerves within the body
JP2019510039A (en) 2016-03-28 2019-04-11 イントラ−セルラー・セラピーズ・インコーポレイテッドIntra−Cellular Therapies, Inc. Novel compositions and methods
WO2017196857A1 (en) * 2016-05-10 2017-11-16 Medicinova, Inc. Treatment of alcoholism and depression and/or dysphoric mood using ibudilast
CA3023014C (en) * 2017-11-06 2023-09-26 Stalicla Sa Pharmaceutical composition for treatment of autism
JP7401442B2 (en) * 2018-01-31 2023-12-19 イントラ-セルラー・セラピーズ・インコーポレイテッド new use
US11766296B2 (en) 2018-11-26 2023-09-26 Augmedics Ltd. Tracking system for image-guided surgery
CN111803487B (en) * 2019-04-10 2022-12-02 成都百裕制药股份有限公司 Application of ginkgolide in preparation of medicine for preventing and/or treating Guillain-Barre syndrome
US20220193030A1 (en) * 2019-04-10 2022-06-23 Chengdu Baiyu Pharmaceutical Co., Ltd. Use of ginkgo terpene lactone in preparing drug for preventing and/or treating guillain-barre-strohl syndrome
US11382712B2 (en) 2019-12-22 2022-07-12 Augmedics Ltd. Mirroring in image guided surgery
US11839622B1 (en) 2020-01-15 2023-12-12 Randall Lewarchik Consumable nutraceutical composition
WO2022047070A1 (en) * 2020-08-27 2022-03-03 University Of Central Florida Research Foundation, Inc. Combination drug treatment to increase neurogenesis for neurological disorders
EP4281065A1 (en) * 2021-01-20 2023-11-29 Alto Neuroscience, Inc. Enhancement of camp signaling as a combination drug strategy for the treatment of depression and related conditions
US11896445B2 (en) 2021-07-07 2024-02-13 Augmedics Ltd. Iliac pin and adapter
WO2024013505A1 (en) * 2022-07-13 2024-01-18 Healx Ltd Ibudilast and gaboxadol for the treatment of fragile x syndrome

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004014911A1 (en) * 2002-08-08 2004-02-19 Memory Pharmaceuticals Corporation Phosphodiesterase 4 inhibitors
EP1579862A1 (en) * 2004-03-25 2005-09-28 Boehringer Ingelheim Vetmedica Gmbh Use of PDE III inhibitors for the reduction of heart size in mammals suffering from heart failure
WO2006050057A2 (en) * 2004-10-28 2006-05-11 Celgene Corporation Methods and compositions using pde4 modulators for treatment and management of central nervous system injury
WO2007030697A2 (en) * 2005-09-07 2007-03-15 Braincells, Inc. Modulation of neurogenesis by hdac inhibition

Family Cites Families (714)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3121076A (en) 1964-02-11 Benzodiazepinones and processes
US3109843A (en) 1963-11-05 Process for preparing
US666073A (en) 1900-10-29 1901-01-15 Harry Simmons Sectional legal-blank file.
GB235187A (en) 1924-06-07 1926-06-03 Robert Howe Gould Improvements in burglar and like alarms
US1873732A (en) 1928-12-28 1932-08-23 Abbott Lab Bactericide applicable to acid-fast bacteria
US3136815A (en) 1959-12-10 1964-06-09 Hoffmann La Roche Amino substituted benzophenone oximes and derivatives thereof
US3371085A (en) 1959-12-10 1968-02-27 Hoffmann La Roche 5-aryl-3h-1,4-benzodiazepin-2(1h)-ones
US3454554A (en) 1960-10-14 1969-07-08 Colgate Palmolive Co Aminoalkyliminodibenzyl compounds
US3116203A (en) 1962-03-14 1963-12-31 Hoffmann La Roche Oleaginous systems
NL298071A (en) 1963-06-04
CH449645A (en) 1963-07-09 1968-01-15 Ciba Geigy Process for the production of new amino acids
CH427803A (en) 1963-12-06 1967-01-15 Geigy Ag J R Process for the production of a new isoxazole derivative
NL129434C (en) 1966-03-12
US3397209A (en) 1966-11-25 1968-08-13 Geigy Chem Corp 3-hydroxy-5-isoxazole-carboxamide
US3885046A (en) 1969-12-04 1975-05-20 Burroughs Wellcome Co Meta chloro or fluoro substituted alpha-T-butylaminopropionphenones in the treatment of depression
BE759838A (en) 1969-12-04 1971-06-03 Wellcome Found KETONES WITH BIOLOGICAL ACTIVITY
FR2077918B1 (en) 1970-02-24 1973-04-06 Berthier Laboratoires
US3758528A (en) 1970-03-13 1973-09-11 Science Union & Cie Tricyclic compounds
US3821249A (en) 1970-03-13 1974-06-28 En Nom Collectif Science Union Dibenzothiazefin derivatives
US3819631A (en) 1970-12-15 1974-06-25 May & Baker Ltd Azapurinones
OA04285A (en) 1972-01-07 1979-12-31 Rhone Poulenc Sa New derivatives of pyrrolo (3,4-b) pyrazine and their preparation.
US3932407A (en) 1973-11-19 1976-01-13 Bristol-Myers Company Optionally substituted 1,2,3,5-tetrahydroimidezo(2,1-b)-quinazolin-2-ones and 6(H)-1,2,3,4-tetrahydropyimido(2,1-b)quinazolin-2-ones
USRE31617E (en) 1972-02-04 1984-06-26 Bristol-Myers Company Optionally substituted 1,2,3,5-tetrahydroimidezo(2,1-b)-quinazolin-2-ones and 6(H)-1,2,3,4-tetrahydropyimido(2,1-b)quinazolin-2-ones
US4036840A (en) 1972-06-07 1977-07-19 Icn Pharmaceuticals 2-Substituted-s-triazolo[1,5a]pyrimidines
GB1457873A (en) 1973-01-04 1976-12-08 Allen & Hanburys Ltd Imidazotriazines
GB1422263A (en) 1973-01-30 1976-01-21 Ferrosan As 4-phenyl-piperidine compounds
US4051236A (en) 1973-02-15 1977-09-27 E. R. Squibb & Sons, Inc. Inhibition of blood platelet aggregation
US4194009A (en) 1974-01-10 1980-03-18 Eli Lilly And Company Aryloxyphenylpropylamines for obtaining a psychotropic effect
US4314081A (en) 1974-01-10 1982-02-02 Eli Lilly And Company Arloxyphenylpropylamines
US4280957A (en) 1974-09-11 1981-07-28 Hoffmann-La Roche Inc. Imidazodiazepines and processes therefor
AR208414A1 (en) 1974-11-07 1976-12-27 Rhone Poulenc Ind PROCEDURE TO OBTAIN NEW DERIVATIVES OF ((ACIL-4PIPERAZINIL-1) CARBONYLOXI-5 PYRROLINONE-2)
US4093617A (en) 1974-11-12 1978-06-06 Icn Pharmaceuticals, Inc. 3,5,7-Trisubstituted pyrazolo[1,5-a]pyrimidines
DE2460891C2 (en) 1974-12-21 1982-09-23 Gödecke AG, 1000 Berlin 1-aminomethyl-1-cycloalkaneacetic acids and their esters, processes for their preparation and medicaments containing these compounds
US3960927A (en) 1975-03-18 1976-06-01 Richardson-Merrell Inc. Olefinic derivatives of amino acids
NL7503310A (en) 1975-03-20 1976-09-22 Philips Nv CONNECTIONS WITH ANTIDEPRESSIVE ACTION.
NL189199C (en) 1975-04-05 1993-02-01 Akzo Nv PROCESS FOR THE PREPARATION OF PHARMACEUTICAL PREPARATIONS WITH ACTION ON THE CENTRAL NERVOUS SYSTEM BASED ON BENZ (ARYL) AZEPINE DERIVATIVES, THE PHARMACEUTICAL PREPARATIONS OBTAINED, AND METHOD FOR PREPARING THE PRODUCT TO BE USED.
FR2319338A1 (en) 1975-08-01 1977-02-25 Synthelabo NEW A-PHENYL BENZYLIDENIC DERIVATIVES OF AMINO ACIDS, THEIR PREPARATION AND THE MEDICINAL PRODUCTS CONTAINING THEM
GB1526331A (en) 1976-01-14 1978-09-27 Kefalas As Phthalanes
YU96177A (en) 1976-04-24 1982-08-31 Wuelfing Johann A Process for obtaining adenine derivatives
US4107307A (en) 1977-02-03 1978-08-15 American Cyanamid Company Imidazo [1,5-d]-as-triazine-4(3H)-ones and thiones
USRE30511E (en) 1977-02-03 1981-02-10 American Cyanamid Company Imidazo[1,5-d]-as-triazine-4(3H)-ones and thiones
US4404380A (en) 1977-02-14 1983-09-13 Mead Johnson & Company Triazolopyrimidines
CA1095906A (en) 1977-02-14 1981-02-17 Davis L. Temple, Jr. Heterocyclopyrimidines, compositions and therapeutic process
US4107309A (en) 1977-05-23 1978-08-15 American Cyanamid Company Substituted imidazo[1,2-d]-as-triazines
US4096257A (en) 1977-05-23 1978-06-20 American Cyanamid Company Substituted imidazo [1,2-d]-as-triazines
IN148482B (en) 1977-06-03 1981-03-07 Pfizer
DK270278A (en) 1977-06-20 1978-12-21 Krogsgaard Larsen P CYCLIC AMINO ACIDS
CA1086735A (en) 1977-11-03 1980-09-30 John C. Danilewicz Piperidino-quinazolines
US4370328A (en) 1977-11-03 1983-01-25 Pfizer Inc. Cardiac stimulant 1-(3- or 4-substituted piperidino)phthalazines
IL56369A (en) 1978-01-20 1984-05-31 Erba Farmitalia Alpha-phenoxybenzyl propanolamine derivatives,their preparation and pharmaceutical compositions comprising them
US4146718A (en) 1978-04-10 1979-03-27 Bristol-Myers Company Alkyl 5,6-dichloro-3,4-dihydro-2(1h)-iminoquinazoline-3-acetate hydrohalides
JPS5510608A (en) 1978-07-07 1980-01-25 Kokusai Denshin Denwa Co Ltd <Kdd> Coordinate reader
US4366156A (en) 1979-03-05 1982-12-28 Mead Johnson & Company Antiallergic methods using diazaheterocyclopurines
CA1143728A (en) 1979-10-04 1983-03-29 Max Gerecke Imidazodiazepine derivatives
US4536518A (en) 1979-11-01 1985-08-20 Pfizer Inc. Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine
JPS5668695A (en) 1979-11-10 1981-06-09 Sankyo Co Ltd Enzyme inhibitor griseolic acid and its preparation
US4642345A (en) 1980-08-14 1987-02-10 Mead Johnson & Company 6,7-dihydro-3H-imidazo[1,2-a]-purine-9(4H)-ones
US4301176A (en) 1980-08-18 1981-11-17 Warner-Lambert Company Method of administering calcium valproate
US4361583A (en) 1980-08-19 1982-11-30 Synthelabo Analgesic agent
FR2492258A1 (en) 1980-10-17 1982-04-23 Pharmindustrie NEW AMINO-2 TRIFLUOROMETHOXY-6 BENZOTHIAZOLE-BASED MEDICINAL PRODUCT
FR2492382A1 (en) 1980-10-22 1982-04-23 Synthelabo IMIDAZO (1,2-A) PYRIDINE DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC USE THEREOF
US4489078A (en) 1980-11-24 1984-12-18 Mead Johnson & Company Diazaheterocyclopurines used as anti-broncho spasmatics and vasodilators
US4338317A (en) 1981-03-16 1982-07-06 Mead Johnson & Company Phenoxyethyl-1,2,4,-triazol-3-one antidepressants
US4383999A (en) 1981-05-26 1983-05-17 Smithkline Beckman Corporation Inhibition of GABA uptake by N-substituted azaheterocyclic carboxylic acids and their esters
FR2508035A1 (en) 1981-06-23 1982-12-24 Fabre Sa Pierre ARYL-1-AMINOMETHYL-2 CYCLOPROPANES CARBOXAMIDE (Z) DERIVATIVES, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS USEFUL IN THE TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS
LU83729A1 (en) 1981-11-04 1983-09-01 Galephar VALPROIC ACID SALTS, THEIR PREPARATION AND THEIR USE
US4513135A (en) 1982-03-05 1985-04-23 Eli Lilly And Company Diaryl-pyrazine derivatives affecting GABA binding
CH655110A5 (en) 1982-09-03 1986-03-27 Otsuka Pharma Co Ltd CARBOSTYRILE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING THEM.
US4663320A (en) 1983-02-16 1987-05-05 Syntex (U.S.A.) Inc. (2-oxo-1,2,3,5-tetrahydroimidazo[2,1-b]quinoazolinyl)oxyalkylamides, compositions and the use thereof
US4490371A (en) 1983-02-16 1984-12-25 Syntex (U.S.A.) Inc. N,N-Disubstituted-(2-oxo-1,2,3,5-tetrahydroimidazo-[2,1-B]quinazolinyl)oxyalkylamides
US4626538A (en) 1983-06-23 1986-12-02 American Cyanamid Company [7-(3-disubstituted amino)phenyl]pyrazolo[1,5-a]pyrimidines
US4521422A (en) 1983-06-23 1985-06-04 American Cyanamid Company Aryl and heteroaryl[7-(aryl and heteroaryl)pyrazolo[1,5-a]pyrimidin-3-yl]methanones
US4900836A (en) 1983-06-23 1990-02-13 American Cyanamid Company (3-amino-1H-pyrazol-4-yl) (aryl)methanones
US4513006A (en) 1983-09-26 1985-04-23 Mcneil Lab., Inc. Anticonvulsant sulfamate derivatives
US4761501A (en) 1983-10-26 1988-08-02 American Home Products Corporation Substituted phenylacetamides
US4593029A (en) 1984-02-15 1986-06-03 Syntex (U.S.A.) Inc. Novel ω-(N-imidazolyl)alkyl ethers of 1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-2-ones
GB8425872D0 (en) 1984-10-12 1984-11-21 Ciba Geigy Ag Chemical compounds
CA1272408A (en) 1985-02-13 1990-08-07 Goro Mizuno Display device
US4855290A (en) 1985-05-10 1989-08-08 State Of Israel, Represented By Prime Minister's Office, Israel Institute For Biological Research Derivatives of quinuclidine
DK288385D0 (en) 1985-06-26 1985-06-26 Novo Industri As AMINO ACID DERIVATIVES
PT83530B (en) 1985-10-17 1989-05-31 Smith Kline French Lab PREPARATION PROCESS OF PYRIDONE DERIVATIVES, IN PARTICULAR PHENYLER DERIVATIVES
US4670434A (en) 1985-11-14 1987-06-02 Syntex (U.S.A.) Inc. (2-oxo-3-methylene-1,2,3,5-tetrahydroimidazo[2,1-b]quinazolinyl)oxyalkylamides useful as cyclic AMP phosphodiesterase inhibitors
US4775674A (en) 1986-05-23 1988-10-04 Bristol-Myers Company Imidazoquinolinylether derivatives useful as phosphodiesterase and blood aggregation inhibitors
FR2600650B1 (en) 1986-06-27 1988-09-09 Synthelabo PROCESS FOR THE PREPARATION OF IMIDAZOPYRIDINES AND INTERMEDIATE COMPOUNDS
US4701459A (en) 1986-07-08 1987-10-20 Bristol-Myers Company 7-amino-1,3-dihydro-2H-imidazo[4,5-b]quinolin 2-ones and method for inhibiting phosphodiesterase and blood platelet aggregation
US4709094A (en) 1986-07-10 1987-11-24 State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon Sigma brain receptor ligands and their use
US5093525A (en) 1986-07-10 1992-03-03 State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University N,N'-disubstituted guanidines and their use as excitatory amino acid antagonists
US5502255A (en) 1986-07-10 1996-03-26 State Of Oregon Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon Substituted guanidines having high binding to the sigma receptor and the use thereof
US5312840A (en) 1986-07-10 1994-05-17 State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education Substituted guanidines having high binding to the sigma receptor and the use thereof
US4761416A (en) 1986-07-25 1988-08-02 Syntex (U.S.A.) Inc. N-N-disubstituted-ω-[2-amino-3-(carbonylmethyl)-3, 4-dihydroquinazolinyl]oxyalkylamides and related compounds
US4739056A (en) 1986-11-26 1988-04-19 Syntex (U.S.A.) Inc. N-N-disubstituted-omega-(2-amino-3-(carbonylmethyl)-3,4-dihydroquinazolinyl)oxy-alkylamides and related compounds
US4710508A (en) 1986-12-08 1987-12-01 Warner-Lambert Company O-substituted tetrahydropyridine oxime cholinergic agents
US4786648A (en) 1986-12-08 1988-11-22 Warner-Lambert Company O-substituted tetrahydropyridine oxime cholinergic agents
US4956388A (en) 1986-12-22 1990-09-11 Eli Lilly And Company 3-aryloxy-3-substituted propanamines
US4721784A (en) 1986-12-22 1988-01-26 Ortho Pharmaceutical Corporation 6-benzoxazinyl-2,3,4,5-tetrahydropyridazin-3-ones
US5081242A (en) 1986-12-22 1992-01-14 Ortho Pharmaceutical Corporation 6-benzoxazinyl- and 6-benzothiazinyl 2,3,4,5-tetrahydropyridazin-3-ones
US4766118A (en) 1986-12-22 1988-08-23 Ortho Pharmaceutical Corporation 6-benzoxazinyl- and 6-benzothiazinyl-2,3,4,5-tetrahydropyridazin-3-ones and pharmaceutical use
US4929734A (en) 1987-03-31 1990-05-29 Warner-Lambert Company Tetrahydropyridine oxime compounds
GB8714789D0 (en) 1987-06-24 1987-07-29 Lundbeck & Co As H Heterocyclic compounds
US4981858A (en) 1987-08-13 1991-01-01 State Of Israel, Represented By The Prime Minister's Office, Israel Institute For Biological Research Optical isomers
USRE35517E (en) 1987-08-25 1997-05-20 University Of Southern California Method, compositions, and compounds for modulating brain excitability
US5232917A (en) 1987-08-25 1993-08-03 University Of Southern California Methods, compositions, and compounds for allosteric modulation of the GABA receptor by members of the androstane and pregnane series
US5319115A (en) 1987-08-25 1994-06-07 Cocensys Inc. Method for making 3α-hydroxy, 3β-substituted-pregnanes
US5120723A (en) 1987-08-25 1992-06-09 University Of Southern California Method, compositions, and compounds for modulating brain excitability
EP0311313B1 (en) 1987-10-05 1995-05-10 Yamanouchi Pharmaceutical Co. Ltd. Heterocyclic spiro compounds and their preparation
US5412096A (en) 1987-10-05 1995-05-02 Yamanouchi Pharmaceutical Co., Ltd. Hydrochloride salts of heterocyclic spiro compounds
IL88156A (en) 1987-11-13 1997-02-18 Novo Nordisk As Azacyclic compounds their preparation and pharmaceutical compositions containing them
US4831031A (en) 1988-01-22 1989-05-16 Pfizer Inc. Aryl piperazinyl-(C2 or C4) alkylene heterocyclic compounds having neuroleptic activity
US5091431A (en) 1988-02-08 1992-02-25 Schering Corporation Phosphodiesterase inhibitors
US4957916A (en) 1988-08-05 1990-09-18 Janssen Pharmaceutica N.V. Antipsychotic 3-piperazinylbenzazole derivatives
GB8820266D0 (en) 1988-08-26 1988-09-28 Smith Kline French Lab Compounds
US4861891A (en) 1988-08-31 1989-08-29 Pfizer Inc. Antidepressant N-substituted nicotinamide compounds
FR2636625B1 (en) 1988-09-01 1990-11-09 Jouveinal Sa DISUBSTITUTED BENZYLAMINES, PROCESS FOR THEIR PREPARATION, THEIR USE AS A MEDICAMENT AND THEIR SYNTHESIS INTERMEDIATES
DE8817121U1 (en) 1988-11-22 1993-02-04 Boehringer Ingelheim Kg, 6507 Ingelheim, De
US5286864A (en) 1988-11-22 1994-02-15 Boehringer Ingelheim Kg Quinuclidines, their use as medicaments and processes for their preparation
US5043345A (en) 1989-02-22 1991-08-27 Novo Nordisk A/S Piperidine compounds and their preparation and use
US4981870A (en) 1989-03-07 1991-01-01 Pfizer Inc. Use of 4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine derivatives in the treatment of psychosis, inflammation and as immunosuppressants
US4971972A (en) 1989-03-23 1990-11-20 Schering Corporation Phosphodiesterase inhibitors having an optionally substituted purine derivative portion and a benzo- or cyclopenta-furan portion
US5278170A (en) 1989-04-13 1994-01-11 Beecham Group P.L.C. Azabicylo oxime compounds
DK0392803T3 (en) 1989-04-13 2004-10-18 Beecham Group Plc Hitherto unknown compounds
AU642881B2 (en) 1989-05-02 1993-11-04 State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon Methods for treating anxiety with sigma receptor ligands
US4956368A (en) 1989-07-24 1990-09-11 Bristol-Myers Company Metabolites and prodrug formulations of 8-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl]-8-azaspiro[4.5]decane-7,9-dione
US5109002A (en) 1989-09-08 1992-04-28 Du Pont Merck Pharmaceutical Company Antipsychotic 1-cycloalkylpiperidines
CA2069318A1 (en) 1989-10-27 1991-04-28 Engelbert Ciganek (n-phthalimidoalkyl) piperidines
US4943573A (en) 1989-11-01 1990-07-24 Bristol-Myers Squibb Company Imidazo[4,5-b]quinolinyloxyalkanoic acid amides with enhanced water solubility
US4963561A (en) 1990-02-28 1990-10-16 Sterling Drug Inc. Imidazopyridines, their preparation and use
US5010086A (en) 1990-02-28 1991-04-23 Sterling Drug Inc. Imidazopyridines, compositions and use
US5149817A (en) 1990-03-05 1992-09-22 Shionogi & Co., Ltd. Teirahydropyridine derivatives
US5169855A (en) 1990-03-28 1992-12-08 Du Pont Merck Pharmaceutical Company Piperidine ether derivatives as psychotropic drugs or plant fungicides
US5116995A (en) 1990-05-25 1992-05-26 Taisho Pharmaceutical Co., Ltd. Carbazole compounds
WO1991018868A1 (en) 1990-05-25 1991-12-12 STATE OF OREGON, acting by and through the OREGON STATE BOARD OF HIGHER EDUCATION, acting for and onbehalf of the OREGON HEALTH SCIENCES UNIVERSITY Substituted guanidines having high binding to the sigma receptor and the use thereof
US5612211A (en) 1990-06-08 1997-03-18 New York University Stimulation, production and culturing of hematopoietic progenitor cells by fibroblast growth factors
FR2663328B1 (en) 1990-06-14 1994-08-05 Sanofi Sa DERIVATIVES OF HEXAHYDROAZEPINES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
US5250534A (en) 1990-06-20 1993-10-05 Pfizer Inc. Pyrazolopyrimidinone antianginal agents
US5095015A (en) 1990-07-24 1992-03-10 Neurogen Corporation Certain azacycloalkyl imidazopyrimidines; a new class of gaba brain receptor ligands
FR2663934B1 (en) 1990-06-27 1994-06-03 Adir NOVEL DERIVATIVES OF ACID 4 - BUTYRIC AMINO, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL PREPARATIONS CONTAINING THEM.
JP2935541B2 (en) 1990-06-28 1999-08-16 サントリー株式会社 Fused heterocyclic compound
US5086054A (en) 1990-07-31 1992-02-04 Sri International Novel arylcycloalkanepolyalkylamines
DK198590D0 (en) 1990-08-21 1990-08-21 Novo Nordisk As HETEROCYCLIC COMPOUNDS, THEIR PREPARATION AND USE
GB9019095D0 (en) 1990-09-01 1990-10-17 Beecham Group Plc Novel compounds
US5185446A (en) 1990-09-04 1993-02-09 Neurogen Corporation Certain cycloalkyl imidazopyrimidines; a new class of gaba brainreceptor ligands
EP0738717A1 (en) 1990-10-09 1996-10-23 Neurogen Corporation Certain substituted pyrimidines as intermediates for production of cycloalkyl and azacycloalkyl pyrrolopyrimidines
CA2093823A1 (en) 1990-10-12 1992-04-13 Steven M. Bromidge 1,2,5,6-tetrahydropyridine oxime derivatives
ES2068453T3 (en) 1990-10-15 1995-04-16 Nestle Sa BLACK TEA TREATMENT.
US5139802A (en) 1990-10-15 1992-08-18 Nestec S.A. Oxidation of tea
US5744602A (en) 1990-10-31 1998-04-28 Neurogen Corporation Certain imidazoquinoxalines; a new class of GABA brain receptor ligands
US6268496B1 (en) 1990-10-31 2001-07-31 Neurogen Corporation Certain imidazoquinoxalines: a new class of GABA brain receptor ligands
US5130430A (en) 1990-10-31 1992-07-14 Neurogen Corporation 2-substituted imidazoquinoxaline diones, a new class of gaba brain receptor ligands
US5116837A (en) 1990-12-21 1992-05-26 Ortho Pharmaceutical Corporation 2,9-dihydro-(6 or 7)-(3-oxo-2,3,4,5-tetrahydropyridazinyl)-pyrazolo [4,3-B]-1,4-benzoxazines
US5180729A (en) 1991-02-22 1993-01-19 Du Pont Merck Pharmaceutical Company Use of sigma receptor antagonists for treatment of cocaine abuse
US5162341A (en) 1991-02-22 1992-11-10 Du Pont Merck Pharmaceutical Company Use of sigma receptor antagonists for treatment of amphetamine abuse
ATE130851T1 (en) 1991-03-14 1995-12-15 Basf Ag SUBSTITUTED N-PHENYLPIPERIDINE AND DRUGS THEREOF.
US5231099A (en) 1991-04-15 1993-07-27 Du Pont Merck Pharmaceutical Company Use of sigma receptor antagonists to enhance the effects of antipsychotic drugs
US5137895A (en) 1991-04-29 1992-08-11 A. H. Robins Company, Incorporated 3-[N-aroyl(or thioaroyl)aminomethyl]-3-quinuclidinols
WO1992020683A1 (en) 1991-05-15 1992-11-26 Yamanouchi Pharmaceutical Co., Ltd. (-)-(s)-2,8-dimethyl-3-methylene-1-oxa-8-azaspiro[4,5]decane l-tartrate
NZ243065A (en) 1991-06-13 1995-07-26 Lundbeck & Co As H Piperidine derivatives and pharmaceutical compositions
AU676993B2 (en) 1991-06-27 1997-04-10 Virginia Commonwealth University Sigma receptor ligands and the use thereof
US5182290A (en) 1991-08-27 1993-01-26 Neurogen Corporation Certain oxazoloquinolinones; a new class of GABA brain receptor ligands
US5182386A (en) 1991-08-27 1993-01-26 Neurogen Corporation Certain imidazoquinoxalinones; a new class of gaba brain receptor ligands
JPH06510999A (en) 1991-09-13 1994-12-08 コセンシス・インコーポレイテッド Novel GABA↓a receptor with steroid binding site
PT100905A (en) 1991-09-30 1994-02-28 Eisai Co Ltd BICYCLE HYGIENEOUS HETEROCYCLIC COMPOUNDS CONTAINING BENZENE, CYCLOHEXAN OR PYRIDINE AND PYRIMIDINE, PYRIDINE OR IMIDAZOLE SUBSTITUTES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
US5369108A (en) 1991-10-04 1994-11-29 Sloan-Kettering Institute For Cancer Research Potent inducers of terminal differentiation and methods of use thereof
US5585490A (en) 1991-10-08 1996-12-17 Neurogen Corporation Certain cycloalkyl and azacycloalkyl pyrrolopyrimidines; a new class of GABA brain receptor ligands
WO1993009094A1 (en) 1991-10-30 1993-05-13 The Du Pont Merck Pharmaceutical Company Ether derivatives of alkyl piperidines and pyrrolidines as antipsychotic agents
PH31245A (en) 1991-10-30 1998-06-18 Janssen Pharmaceutica Nv 1,3-Dihydro-2H-imidazoÄ4,5-BÜ-quinolin-2-one derivatives.
US5212310A (en) 1991-12-19 1993-05-18 Neurogen Corporation Certain aryl fused imidazopyrimidines; a new class of GABA brain receptor ligands
US5243049A (en) 1992-01-22 1993-09-07 Neurogen Corporation Certain pyrroloquinolinones: a new class of GABA brain receptor ligands
MX9300875A (en) 1992-02-20 1993-08-31 Smithkline Beecham Plc PROCEDURE FOR THE PREPARATION OF AZABICICLIC COMPOUNDS.
US6225115B1 (en) 1992-03-04 2001-05-01 Synaptic Pharmaceutical Corporation DNA encoding taurine and GABA transporters and uses thereof
US5298657A (en) 1992-03-20 1994-03-29 Cambridge Neuroscience Inc. Preparation of substituted guanidines
US5294612A (en) 1992-03-30 1994-03-15 Sterling Winthrop Inc. 6-heterocyclyl pyrazolo [3,4-d]pyrimidin-4-ones and compositions and method of use thereof
WO1994025463A1 (en) 1992-04-08 1994-11-10 Neurogen Corporation Certain aryl fused pyrrolopyrimidines; a new class of gaba brain receptor ligands
US5367077A (en) 1992-04-08 1994-11-22 Neurogen Corporation Certain cycloalkyl and azacycloalkyl pyrrolopyridines; a new class of gaba rain receptor ligands
US5266698A (en) 1992-04-30 1993-11-30 Neurogen Corporation Certain aryl and cycloalkyl fused imidazopyrazinediones; a new class of GABA brain receptor ligands
ES2060547B1 (en) 1992-06-04 1995-06-16 Ferrer Int IMPROVEMENTS IN THE PURPOSE OF THE INVENTION PATENT N / 9201158 THAT REFERS TO "PROCEDURE FOR OBTAINING NEW DERIVATIVES OF 4-BENCILPIPERIDINE".
GB9212693D0 (en) 1992-06-15 1992-07-29 Celltech Ltd Chemical compounds
GB9212673D0 (en) 1992-06-15 1992-07-29 Celltech Ltd Chemical compounds
JP2683783B2 (en) 1992-07-10 1997-12-03 雪印乳業株式会社 Agent for Sjogren's syndrome
JP2657760B2 (en) 1992-07-15 1997-09-24 小野薬品工業株式会社 4-aminoquinazoline derivatives and pharmaceuticals containing them
US5672499A (en) 1992-07-27 1997-09-30 California Institute Of Technology Immoralized neural crest stem cells and methods of making
US5306819A (en) 1992-08-27 1994-04-26 Neurogen Corporation Certain aryl a cycloalkyl fused imidazopyrazinols; and new class of GABA brain receptor ligands
ZA937382B (en) 1992-10-06 1994-04-29 Warner Lambert Co Novel composition for peroral therapy of cognitionimpairment and a process therefor
GB9222253D0 (en) 1992-10-23 1992-12-09 Celltech Ltd Chemical compounds
US5668283A (en) 1992-11-12 1997-09-16 Neurogen Corporation Certain aryl substituted pyrrolopyrazines; a new class of GABA brain receptor ligands
US5286860A (en) 1992-11-12 1994-02-15 Neurogen Corporation Certain aryl substituted pyrrolopyrazines; a new class of GABA brain receptor ligands
US5814651A (en) 1992-12-02 1998-09-29 Pfizer Inc. Catechol diethers as selective PDEIV inhibitors
US5622977A (en) 1992-12-23 1997-04-22 Celltech Therapeutics Limited Tri-substituted (aryl or heteroaryl) derivatives and pharmaceutical compositions containing the same
GB9226830D0 (en) 1992-12-23 1993-02-17 Celltech Ltd Chemical compounds
WO1994015937A1 (en) 1993-01-06 1994-07-21 Neurogen Corporation Certain aryl substituted imidazopyrazinones a new class of gaba brain receptor ligands
US5362860A (en) 1993-02-01 1994-11-08 Warner-Lambert Company Neutral stabilization complex for CI-979 HCl, a cognition activator
US5424301A (en) 1993-02-01 1995-06-13 Warner-Lambert Company Starch stabilized o-substituted tetrahydropyridine oxime cholinergic agents
US6013799A (en) 1993-03-03 2000-01-11 Neurogen Corporation Certain cycloalkyl imidazopyrimides, a new class of gaba brain receptor ligands
GB9304920D0 (en) 1993-03-10 1993-04-28 Celltech Ltd Chemical compounds
GB9304919D0 (en) 1993-03-10 1993-04-28 Celltech Ltd Chemical compounds
CA2158952C (en) 1993-03-26 1999-05-18 Shen-Chun Kuo 2-substituted morpholine and thiomorpholine derivatives as gaba-b antagonists
US5455252A (en) 1993-03-31 1995-10-03 Syntex (U.S.A.) Inc. Optionally substituted 6,8-quinolines
EP0701444B1 (en) 1993-05-24 2010-04-07 Purdue Pharma Ltd. Methods and compositions for inducing sleep
US5750702A (en) 1993-10-27 1998-05-12 Neurogen Corporation Certain pyrrolo pyridine-3-carboxamides; a new class of GABA brain receptor ligands
JP3610368B2 (en) 1993-05-27 2005-01-12 セネス リミティド Therapeutic substituted guanidine
GB9311920D0 (en) 1993-06-09 1993-07-28 Pfizer Ltd Therapeutic agents
US6087346A (en) 1993-06-23 2000-07-11 Cambridge Neuroscience, Inc. Sigma receptor ligands and the use thereof
WO1995001338A1 (en) 1993-07-02 1995-01-12 Byk Gulden Lomberg Chemische Fabrik Gmbh Fluoroalkoxy-substituted benzamides and their use as cyclic nucleotide phosphodiesterase inhibitors
WO1995001997A1 (en) 1993-07-09 1995-01-19 Smithkline Beecham Corporation RECOMBINANT AND HUMANIZED IL-1β ANTIBODIES FOR TREATMENT OF IL-1 MEDIATED INFLAMMATORY DISORDERS IN MAN
ES2074946B1 (en) 1993-07-19 1996-06-16 Ferrer Int NEW COMPOUNDS DERIVED FROM 1,2-ETHANODIAMINE-N, N, N ', N'-TETRAS-SUBSTITUTED.
KR100299734B1 (en) 1993-07-28 2002-01-09 모리타 다카카즈 1,4- (diphenylalkyl) piperazine derivative
US5665754A (en) 1993-09-20 1997-09-09 Glaxo Wellcome Inc. Substituted pyrrolidines
US5484944A (en) 1993-10-27 1996-01-16 Neurogen Corporation Certain fused pyrrolecarboxanilides and their use as GABA brain receptor ligands
ATE187447T1 (en) 1993-11-26 1999-12-15 Pfizer 3-PHENYL-2-ISOXAZOLINE DERIVATIVES AS ANTI-INFLAMMATORY AGENTS
WO1995014681A1 (en) 1993-11-26 1995-06-01 Pfizer Inc. Isoxazoline compounds as antiinflammatory agents
US5502072A (en) 1993-11-26 1996-03-26 Pfizer Inc. Substituted oxindoles
FR2713639B1 (en) 1993-12-09 1996-08-30 Irj New derivatives of 2-arylalkenyl-azacycloalkanes ligands to sigma receptors, their preparation process and their use in therapy.
US5500420A (en) 1993-12-20 1996-03-19 Cornell Research Foundation, Inc. Metabotropic glutamate receptor agonists in the treatment of cerebral ischemia
GB9326699D0 (en) 1993-12-22 1994-03-02 Celltech Ltd Chemical compounds
GB9326173D0 (en) 1993-12-22 1994-02-23 Celltech Ltd Chemical compounds and process
WO1995017399A1 (en) 1993-12-22 1995-06-29 Celltech Therapeutics Limited Trisubstituted phenyl derivatives, processes for their preparation and their use as phosphodiesterase (type iv) inhibitors
US7060450B1 (en) 1993-12-30 2006-06-13 President And Fellows Of Harvard College Screening assays for agonists and antagonists of the hedgehog signaling pathway
GB9514465D0 (en) 1995-07-14 1995-09-13 Glaxo Lab Sa Chemical compounds
GB9401090D0 (en) 1994-01-21 1994-03-16 Glaxo Lab Sa Chemical compounds
US5939545A (en) 1994-02-14 1999-08-17 Cocensys, Inc. Method, compositions, and compounds for allosteric modulation of the gaba receptor by members of the androstane and pregnane series
DK0752860T3 (en) 1994-02-14 2000-11-13 Euro Celtique Sa Androstans and pregnans for allosteric modulation of GABA receptor
US5783575A (en) 1994-03-14 1998-07-21 Novo Nordisk A/S Antagonists, their preparation and use
US5696148A (en) 1994-03-14 1997-12-09 Novo Nordisk A/S Indole compounds and their use in treating diseases of the central nervous system
JPH09510223A (en) 1994-03-14 1997-10-14 ノボ ノルディスク アクティーゼルスカブ Heterocyclic compounds, their preparation and use
US5637617A (en) 1994-04-01 1997-06-10 The Regents Of The University Of California Methods for use of GABAa receptor GABAergic compounds
GB9409705D0 (en) 1994-05-14 1994-07-06 Smithkline Beecham Plc Novel compounds
GB9410877D0 (en) 1994-05-31 1994-07-20 Bayer Ag Heterocyclycarbonyl substituted benzoduranyl-and-thiophenyl-alkanecarboxyclic acid derivatives
US5786354A (en) 1994-06-21 1998-07-28 Celltech Therapeutics, Limited Tri-substituted phenyl derivatives and processes for their preparation
US6245774B1 (en) 1994-06-21 2001-06-12 Celltech Therapeutics Limited Tri-substituted phenyl or pyridine derivatives
GB9412571D0 (en) 1994-06-22 1994-08-10 Celltech Ltd Chemical compounds
GB9412573D0 (en) 1994-06-22 1994-08-10 Celltech Ltd Chemical compounds
GB9412672D0 (en) 1994-06-23 1994-08-10 Celltech Ltd Chemical compounds
JP2852608B2 (en) 1994-06-27 1999-02-03 雪印乳業株式会社 Xerostomia treatment
US5661184A (en) 1994-08-12 1997-08-26 Eli Lilly And Company Psychiatric agents
AU3265695A (en) 1994-08-29 1996-03-22 Yamanouchi Pharmaceutical Co., Ltd. Novel naphthyridine derivative and medicinal composition thereof
US5731307A (en) 1994-09-30 1998-03-24 Pfizer, Inc. Neuroleptic 2,7-disubtituted perhydro-1h-pyrido 1, 2-A!pyrazines
US5554645A (en) 1994-10-03 1996-09-10 Mars, Incorporated Antineoplastic cocoa extracts and methods for making and using the same
DE4436509A1 (en) 1994-10-13 1996-04-18 Hoechst Schering Agrevo Gmbh Substituted spiroalkylamino and alkoxy heterocycles, processes for their preparation and their use as pesticides and fungicides
JP3993651B2 (en) 1994-10-21 2007-10-17 アスビオファーマ株式会社 Cyclopropachromene carboxylic acid derivative
US5473077A (en) 1994-11-14 1995-12-05 Eli Lilly And Company Pyrrolidinyl di-carboxylic acid derivatives as metabotropic glutamate receptor agonists
CN1171114A (en) 1994-11-23 1998-01-21 科斯赛斯公司 Androstane and preg nane series for allosteric modulation of gamma-amino-butyric acid receptor
GB9423910D0 (en) 1994-11-26 1995-01-11 Pfizer Ltd Therapeutic agents
GB9423911D0 (en) 1994-11-26 1995-01-11 Pfizer Ltd Therapeutic agents
GB9503601D0 (en) 1995-02-23 1995-04-12 Merck Sharp & Dohme Method of treatment and method of manufacture of medicament
CA2189355A1 (en) 1995-03-01 1996-09-06 Yasuo Onoda Imidazoquinazoline derivatives
US5488055A (en) 1995-03-10 1996-01-30 Sanofi Winthrop Inc. Substituted N-cycloalkylmethyl-1H-pyrazolo(3,4-b)quinolin-4 amines and compositions and methods of use thereof
AU695957B2 (en) 1995-04-21 1998-08-27 Neurosearch A/S Benzimidazole compounds and their use as modulators of the GABA A receptor complex
WO1996034863A1 (en) 1995-05-05 1996-11-07 Novo Nordisk A/S Novel heterocyclic chemistry
DE19518082A1 (en) 1995-05-17 1996-11-21 Merck Patent Gmbh 4 (-Arylaminomethylene) -2,4-dihydropyrazol-3-one
ATE231501T1 (en) 1995-05-18 2003-02-15 Altana Pharma Ag PHENYLDIHYDROBENZOFURANES
JPH11505539A (en) 1995-05-18 1999-05-21 ビイク グルデン ロンベルク ヒェーミッシェ ファブリーク ゲゼルシャフト ミット ベシュレンクテル ハフツング Cyclohexyl dihydrobenzofuran
US6514996B2 (en) 1995-05-19 2003-02-04 Kyowa Hakko Kogyo Co., Ltd. Derivatives of benzofuran or benzodioxole
US5637724A (en) 1995-06-05 1997-06-10 Neurogen Corporation Substituted aryl and cycloalkyl imidazolones; a new class of GABA brain receptor ligands
US5637725A (en) 1995-06-05 1997-06-10 Neurogen Corporation Substituted aryl and cycloalkyl imidazolones; a new class of GABA brain receptor ligands
AU725214B2 (en) 1995-06-06 2000-10-05 Euro-Celtique S.A. Neuroactive steroids of the androstane and pregnane series
US5534522A (en) 1995-06-07 1996-07-09 Warner-Lambert Company (R)-(Z)-1-azabicyclo [2.2.1] heptan-3-one,O-[3-(3-methoxyphenyl)-2-propynyl] oxime maleate as a pharmaceutical agent
US5910590A (en) 1995-06-07 1999-06-08 Neurogen Corporation Certain aryl substituted pyrrolopyrazines; a new class of GABA brain receptor ligands
GB9514464D0 (en) 1995-07-14 1995-09-13 Glaxo Lab Sa Medicaments
AU711755B2 (en) 1995-07-26 1999-10-21 Pfizer Inc. N-(aroyl)glycine hydroxamic acid derivatives and related compounds
US20010018074A1 (en) 1995-07-29 2001-08-30 Smithkline Beecham P.L.C. Process for preparing solid dosage forms of very low-dose drugs
WO1997005137A1 (en) 1995-07-31 1997-02-13 Novo Nordisk A/S Heterocyclic compounds, their preparation and use
DE19533975A1 (en) 1995-09-14 1997-03-20 Merck Patent Gmbh Arylalkyl diazinones
US6166041A (en) 1995-10-11 2000-12-26 Euro-Celtique, S.A. 2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma
JPH11514654A (en) 1995-11-06 1999-12-14 ハー・ルンドベック・アクチェゼルスカベット How to treat brain injury due to trauma
US5800539A (en) 1995-11-08 1998-09-01 Emory University Method of allogeneic hematopoietic stem cell transplantation without graft failure or graft vs. host disease
ZA969485B (en) 1995-11-16 1998-05-12 Lilly Co Eli Excitatory amino acid receptor antagonists.
US5688826A (en) 1995-11-16 1997-11-18 Eli Lilly And Company Excitatory amino acid derivatives
US5912248A (en) 1995-11-16 1999-06-15 Eli Lilly And Company Excitatory amino acid receptor antagonists
IT1276153B1 (en) 1995-11-17 1997-10-27 Roberto Pellicciari GLYCINE DERIVATIVES WITH ANTAGONIST ACTIVITY OF METABOTROPIC GLUTAMATE RECEPTORS
US5710170A (en) 1995-12-15 1998-01-20 Merck Frosst Canada, Inc. Tri-aryl ethane derivatives as PDE IV inhibitors
GB9603723D0 (en) 1996-02-22 1996-04-24 Merck & Co Inc Diphenyl pyridyl derivatives as pde iv inhibitors
GB9526245D0 (en) 1995-12-21 1996-02-21 Celltech Therapeutics Ltd Chemical compounds
GB9526246D0 (en) 1995-12-21 1996-02-21 Celltech Therapeutics Ltd Chemical compounds
GB9526243D0 (en) 1995-12-21 1996-02-21 Celltech Therapeutics Ltd Chemical compounds
US6211365B1 (en) 1996-01-19 2001-04-03 Neurogen Corporation Fused pyrrolecarboxamides; a new class of GABA brain receptor ligands
US5804686A (en) 1996-01-19 1998-09-08 Neurogen Corporation fused pyrrolecarboxamides; a new class of GABA brain receptor ligands
CA2245142C (en) 1996-01-31 2004-11-30 Byk Gulden Lomberg Chemische Fabrik Gmbh New phenanthridines
GB9604926D0 (en) 1996-03-08 1996-05-08 Sandoz Ltd Organic compounds
US5792766A (en) 1996-03-13 1998-08-11 Neurogen Corporation Imidazo 1,5-c! quinazolines; a new class of GABA brain receptor ligands
US5677309A (en) 1996-03-22 1997-10-14 Neurogen Corporation 1,2,4-triazolo 4,3-c! quinazolin-3-ones and 1,2,4-triazolo 4,3-c!quinazolin-3-thiones; a new class of GABA brain receptor ligands
WO1997034870A1 (en) 1996-03-22 1997-09-25 Neurogen Corporation Certain fused pyrrolecarboxamides as gaba brain receptor ligands
US6127378A (en) 1996-03-26 2000-10-03 Byk Gulden Lomberg Chemische Fabrik Gmbh Phenanthridines substituted in the 6 position
US6777217B1 (en) 1996-03-26 2004-08-17 President And Fellows Of Harvard College Histone deacetylases, and uses related thereto
FR2746800B1 (en) 1996-03-29 1998-06-05 Jouveinal Inst Rech DIAZEPINO-INDOLES PHOSPHODIESTERASE INHIBITORS 4
US6297273B1 (en) 1996-04-02 2001-10-02 Mars, Inc. Use of cocoa solids having high cocoa polyphenol content in tabletting compositions and capsule filling compositions
FR2754260B1 (en) 1996-10-04 1998-10-30 Adir NOVEL SUBSTITUTED DERIVATIVES OF BIPHENYL OR PHENYLPYRIDINE, PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
US5723462A (en) 1996-04-26 1998-03-03 Neurogen Corporation Certain fused pyrrolecarboxamides a new class of GABA brain receptor ligands
AP2001002304A0 (en) 1996-05-03 2001-12-31 Pfizer Substituted indazole derivatives and related compounds
DE69711882T2 (en) 1996-05-10 2002-10-31 Icos Corp carboline derivatives
CA2252501A1 (en) 1996-05-20 1997-11-27 Darwin Discovery Limited Quinoline sulfonamides as tnf inhibitors and as pde-iv inhibitors
WO1997044036A1 (en) 1996-05-20 1997-11-27 Darwin Discovery Limited Quinoline carboxamides as tnf inhibitors and as pde-iv inhibitors
CN1219171A (en) 1996-05-20 1999-06-09 达尔文发现有限公司 Benzofuran carboxamides and their therapeutic use
JP4373497B2 (en) 1996-06-19 2009-11-25 ローン−プーラン・ロレ・リミテツド Substituted azabicyclo compounds and their use as inhibitors of TNF and cyclic AMP phosphodiesterase production
DE69723447T2 (en) 1996-06-25 2003-12-24 Pfizer SUBSTITUTED INDAZOL DERIVATIVES AND THEIR USE AS INHIBITORS OF PHOSPHODIESTERASE (PDE) TYPE 4 AND THE TUMOR NECROSIN FACTOR (TNF)
US6017924A (en) 1996-06-27 2000-01-25 Ligand Pharmaceuticals Incorporated Androgen receptor modulator compounds and methods
WO1998000391A1 (en) 1996-06-28 1998-01-08 Nippon Chemiphar Co., Ltd. Cyclopropylglycine derivatives and metabolic-regulation type l-glutamate receptor agonist
GB9614718D0 (en) 1996-07-12 1996-09-04 Bayer Ag 3-ureido-pyridofurans and -pyridothiophenes
DE19628621A1 (en) 1996-07-16 1998-01-22 Byk Gulden Lomberg Chem Fab New 4-substituted benzofuran compounds are phosphodiesterase IV inhibitors
US20020127271A1 (en) 1996-07-25 2002-09-12 Smithkline Beecham P.L.C. Formulation for the treatment and/or prophylaxis of dementia
JP2000515851A (en) 1996-07-25 2000-11-28 メルク シヤープ エンド ドーム リミテツド Substituted triazolopyridazine derivatives as inverse agonists of the GABA lower Aα5 receptor subtype
ES2194205T3 (en) 1996-07-25 2003-11-16 Merck Sharp & Dohme DERIVATIVES OF TRIAZOLO-PIRIDAZINA SUBSTITUTED AS LIGANDOS FOR GABA RECEPTORS.
AU3967297A (en) 1996-08-01 1998-02-25 Cocensys, Inc. Use of gaba and nmda receptor ligands for the treatment of migraine headache
PL331561A1 (en) 1996-08-12 1999-07-19 Yoshitomi Pharmaceutical Pharmaceutic composition containing an inhibitor of rho kinase
DE19632549A1 (en) 1996-08-13 1998-02-19 Merck Patent Gmbh Arylalkanoylpyridazines
DE69717827T2 (en) 1996-08-19 2003-09-04 Altana Pharma Ag BENZOFURAN-4-CARBOXAMIDES
SI0920426T1 (en) 1996-08-26 2004-04-30 Altana Pharma Ag New thiazole derivatives with phosphodiesterase-inhibiting effect
US6312753B1 (en) 1996-09-06 2001-11-06 Mars, Incorporated Cocoa components, edible products having enriched polyphenol content, methods of making same and medical uses
US6015913A (en) 1996-09-06 2000-01-18 Mars, Incorporated Method for producing fat and/or solids from cocoa beans
US20010003588A1 (en) 1996-09-12 2001-06-14 Smithkline Beecham Corporation Controlled release dosage form of [R-(Z)]-alpha-(methoxyimino)-alpha-(1-azabicyclo[2.2.2.]oct-3-yl)acetonitrile monohydrochloride
US5885834A (en) 1996-09-30 1999-03-23 Epstein; Paul M. Antisense oligodeoxynucleotide against phosphodiesterase
ES2196308T3 (en) 1996-10-02 2003-12-16 Janssen Pharmaceutica Nv DERIVED FROM 2-CIANOIMINOIMIDAZOL THAT INHIBIT THE PDE IV.
WO1998016528A1 (en) 1996-10-11 1998-04-23 Chiron Corporation Purine inhibitors of glycogen synthase kinase 3 (gsk3)
DE19642451A1 (en) 1996-10-15 1998-04-16 Merck Patent Gmbh Aminothiophene carboxamides
GB9621789D0 (en) 1996-10-18 1996-12-11 Lilly Industries Ltd Pharmaceutical compounds
WO1998017651A1 (en) 1996-10-21 1998-04-30 Neurosearch A/S 1-phenyl-benzimidazole compounds and their use as baga-a receptor modulators
US5921749A (en) 1996-10-22 1999-07-13 Siemens Westinghouse Power Corporation Vane segment support and alignment device
GB9622386D0 (en) 1996-10-28 1997-01-08 Sandoz Ltd Organic compounds
US6331543B1 (en) 1996-11-01 2001-12-18 Nitromed, Inc. Nitrosated and nitrosylated phosphodiesterase inhibitors, compositions and methods of use
AU711587B2 (en) 1996-11-06 1999-10-14 Darwin Discovery Limited Quinolines and their therapeutic use
US6069151A (en) 1996-11-06 2000-05-30 Darwin Discovery, Ltd. Quinolines and their therapeutic use
WO1998021207A1 (en) 1996-11-12 1998-05-22 Byk Gulden Lomberg Chemische Fabrik Gmbh (2,3-dihydrobenzofuranyl)-thiazoles as phosphodiesterase inhibitors
WO1998022453A1 (en) 1996-11-20 1998-05-28 Byk Gulden Lomberg Chemische Fabrik Gmbh Substituted dihydrobenzofurans as pde inhibitors
US6492554B2 (en) 2000-08-24 2002-12-10 The University Of Tennessee Research Corporation Selective androgen receptor modulators and methods of use thereof
GB9625184D0 (en) 1996-12-04 1997-01-22 Celltech Therapeutics Ltd Chemical compounds
TR199901653T2 (en) 1997-01-15 1999-10-21 Byk Gulden Lomberg Chemische Fabrik Gmbh Phthalazinones.
GB9702524D0 (en) 1997-02-07 1997-03-26 Merck Sharp & Dohme Therapeutic agents
PT975347E (en) 1997-02-28 2008-05-23 Nycomed Gmbh Synergistic combination of pde inhibitors and adenylate cyclase agonists or guanyl cyclyse agonists
ES2131463B1 (en) 1997-04-08 2000-03-01 Lilly Sa DERIVATIVES OF CYCLOPROPYLGLYCIN WITH PHARMACEUTICAL PROPERTIES.
CA2225060A1 (en) 1997-04-09 1998-10-09 Peter Suilun Fong Interactive talking dolls
GB9708945D0 (en) 1997-05-01 1997-06-25 Merck Sharp & Dohme Therapeutic agents
US6387673B1 (en) 1997-05-01 2002-05-14 The Salk Institute For Biological Studies Compounds useful for the modulation of processes mediated by nuclear hormone receptors, methods for the identification and use of such compounds
US6043252A (en) 1997-05-05 2000-03-28 Icos Corporation Carboline derivatives
JP4672820B2 (en) 1997-05-08 2011-04-20 メルク シャープ エンド ドーム リミテッド Substituted 1,2,4-triazolo [3,4-a] phthalazine derivatives as GABAα5 ligands
ZA983930B (en) 1997-05-14 1999-11-08 Lilly Co Eli Excitatory amino acid receptor modulators.
AU7639598A (en) 1997-05-29 1998-12-30 H. Lundbeck A/S Treatment of schizophrenia and psychosis
GB9713707D0 (en) 1997-06-27 1997-09-03 Merck Sharp & Dohme Therapeutic agents
US6825211B1 (en) 1997-07-18 2004-11-30 Georgetown University Bicyclic metabotropic glutamate receptor ligands
EP1000015A1 (en) 1997-07-18 2000-05-17 Georgetown University Bicyclic metabotropic glutamate receptor ligands
PT1000035E (en) 1997-07-25 2003-04-30 Altana Pharma Ag REPLACED 6-PHENYLPHENANTRIDINS
GB9715977D0 (en) 1997-07-29 1997-10-01 Merck Sharp & Dohme Therapeutic agents
ES2137113B1 (en) 1997-07-29 2000-09-16 Almirall Prodesfarma Sa NEW DERIVATIVES OF TRIAZOLO-PIRIDAZINAS HETEROCICLICOS.
US6107295A (en) 1997-08-01 2000-08-22 Merck Patent Gesellschaft Mit Beschrankter Haftung Arylalkanoyl pyridazines
CN1158281C (en) 1997-08-06 2004-07-21 第一三得利制药株式会社 1-aryl-1,8-naphthylidin-4-one derivative as type IV phosphodiesterase inhibitor
US6143760A (en) 1997-08-25 2000-11-07 Neurogen Corporation Substituted 4-oxo-napthyridine-3-carboxamides: GABA brain receptor ligands
US6207842B1 (en) 1997-10-09 2001-03-27 Mars Incorporated Process for preparing procyanidin(4-6 or 4-8) oligomers and their derivatives
GB9721437D0 (en) 1997-10-10 1997-12-10 Glaxo Group Ltd Heteroaromatic compounds and their use in medicine
US5932465A (en) 1997-10-16 1999-08-03 Icos Corporation Phosphodiesterase 8A
US6156753A (en) 1997-10-28 2000-12-05 Vivus, Inc. Local administration of type III phosphodiesterase inhibitors for the treatment of erectile dysfunction
US6127363A (en) 1997-10-28 2000-10-03 Vivus, Inc. Local administration of Type IV phosphodiesterase inhibitors for the treatment of erectile dysfunction
UA64769C2 (en) 1997-11-07 2004-03-15 Х. Луннбек А/С hydrohalogenides of 1-[4-[1-(4-fluorophenyl)-1H-indole-3-yl]-1-butyl]-spiro[isobenzofuran-1(3H),4'-piperidine]
ID25871A (en) 1997-11-12 2000-11-09 Bayer Ag SUBSTITUTED-2-PHENIL IMIDAZOTRIAZINON
WO1999025353A1 (en) 1997-11-13 1999-05-27 Merck Sharp & Dohme Limited Therapeutic uses of triazolo-pyridazine derivatives
US6429207B1 (en) 1997-11-21 2002-08-06 Nps Pharmaceuticals, Inc. Metabotropic glutamate receptor antagonists and their use for treating central nervous system diseases
US6037470A (en) 1997-12-12 2000-03-14 Euro-Celtique S.A. Purine compounds having PDE IV inhibitory activity and methods of synthesis
IT1296985B1 (en) 1997-12-19 1999-08-03 Zambon Spa BENZAZINIC DERIVATIVES INHIBITORS OF PHOSPHODIESTERASE 4
WO1999036423A1 (en) 1998-01-14 1999-07-22 Merck Sharp & Dohme Limited Triazolo-pyridazine derivatives as ligands for gaba receptors
GB9801210D0 (en) 1998-01-21 1998-03-18 Merck Sharp & Dohme Therapeutic agents
EA002755B1 (en) 1998-01-21 2002-08-29 Мерк Шарп Энд Домэ Лимитед Triazolo-pyridazine derivatives as ligands for gaba receptors
GB9801234D0 (en) 1998-01-21 1998-03-18 Merck Sharp & Dohme Therapeutic agents
GB9801208D0 (en) 1998-01-21 1998-03-18 Merck Sharp & Dohme Therapeutic agents
GB9801202D0 (en) 1998-01-21 1998-03-18 Merck Sharp & Dohme Therapeutic agents
GB9801397D0 (en) 1998-01-22 1998-03-18 Merck Sharp & Dohme Therapeutic agents
CN1156476C (en) 1998-01-29 2004-07-07 第一三得利制药株式会社 1-cycloalkyl-1,8-naphthyridin-4-one derivatives with phosphodiesterase IV inhibitory activity
EP1060251B1 (en) 1998-02-23 2006-06-28 ICOS Corporation Phosphodiesterase 10
AU2881199A (en) 1998-02-26 1999-09-15 Neurogen Corporation Substituted 1,4-dihydro-4-oxonicotinic carboxamides: gaba brain receptor ligands
AU2794099A (en) 1998-02-26 1999-09-15 Neurogen Corporation Substituted cycloalkyl-4-oxonicotinic carboxamides; gaba brain receptor ligands
WO1999043681A1 (en) 1998-02-26 1999-09-02 Neurogen Corporation 4-(4-piperidylmethylamino) substituted heteroaryl fused pyridines: gaba brain receptor ligands
AU2793199A (en) 1998-02-26 1999-09-15 Neurogen Corporation 2-(het-)aryl-4-(cyclic amino substituted) heteroaryl fused pyridine derivatives,their preparation and their use as (ant-)agonists for gaba (a) brain receptors
US6900228B1 (en) 1998-03-10 2005-05-31 Research Triangle Institute Opiate compounds, methods of making and methods of use
US6805883B2 (en) 1998-03-12 2004-10-19 Mars, Incorporated Food products containing polyphenol(s) and L-arginine to stimulate nitric oxide
JP2002506868A (en) 1998-03-13 2002-03-05 ザ ユニバーシティー オブ ブリティッシュ コロンビア Granulatimide derivatives for use in cancer therapy
GB9806102D0 (en) 1998-03-20 1998-05-20 Merck Sharp & Dohme Therapeutic agents
FR2776660B1 (en) 1998-03-27 2000-05-12 Parke Davis DIAZEPINO-INDOLES OF PHOSPHODIESTERASES IV
BR9910130A (en) 1998-04-17 2001-01-09 Kenneth Curry Cuban derivatives as metabotropic glutamate receptor antagonists and process for their preparation
ATE247117T1 (en) 1998-04-20 2003-08-15 Pfizer PYRAZOLOPYRIMIDINONE CGMP PDE5 INHIBITORS FOR THE TREATMENT OF SEXUAL FUNCTION DISORDERS
CN1234705C (en) 1998-04-28 2006-01-04 埃尔比昂股份公司 New hydroxyindoles, their use as phosphodiesterase 4 inhibitors and method for producing same
SI1075477T1 (en) 1998-05-05 2003-08-31 Altana Pharma Ag Novel Benzonaphthyridine-N-oxides
WO1999059409A1 (en) 1998-05-21 1999-11-25 Matsumoto Rae R Compounds and uses thereof
EP0967284A1 (en) 1998-05-28 1999-12-29 Pfizer Limited Phosphodiesterases
US6897305B2 (en) 1998-06-08 2005-05-24 Theravance, Inc. Calcium channel drugs and uses
WO1999064414A1 (en) 1998-06-10 1999-12-16 Byk Gulden Lomberg Chemische Fabrik Gmbh Benzamides with tetrahydrofuranyloxy substitutents as phosphodiesterase 4 inhibitors
DE19826841A1 (en) 1998-06-16 1999-12-23 Merck Patent Gmbh Arylalkanoylpyridazines
GB9813006D0 (en) 1998-06-16 1998-08-12 Merck Sharp & Dohme Therapeutic agents
EP1087968A1 (en) 1998-06-16 2001-04-04 MERCK SHARP &amp; DOHME LTD. Triazolo-pyridine derivatives as ligands for gaba receptors
WO1999065897A1 (en) 1998-06-19 1999-12-23 Chiron Corporation Inhibitors of glycogen synthase kinase 3
CA2336894A1 (en) 1998-07-06 2000-01-13 Byk Gulden Lomberg Chemische Fabrik Gmbh New benzoxazoles with pde-inhibiting activity
ITMI981671A1 (en) 1998-07-21 2000-01-21 Zambon Spa PHTHALAZINIC DERIVATIVES INHIBITORS OF PHOSPHODISTERASE 4
US6177569B1 (en) 1998-08-25 2001-01-23 Neurogen Corporation Oxo-pyridoimidazole-carboxamides: GABA brain receptor ligands
CN1348363A (en) 1998-08-27 2002-05-08 布里斯托尔-米尔斯·斯奎布公司 Novel pharmaceutical salt form
AU746806B2 (en) 1998-08-31 2002-05-02 Taisho Pharmaceutical Co., Ltd. 6-fluorobicyclo(3. 1.0)hexane derivatives
CH694053A5 (en) 1998-09-03 2004-06-30 Hoffmann La Roche Ver method for the production of 2-amino-bicyclo [3.1.0] hexane-2,6-dicarboxylic acid derivatives.
KR20010073099A (en) 1998-09-03 2001-07-31 히라타 다다시 Oxygenic heterocyclic compounds
EP1114048A1 (en) 1998-09-16 2001-07-11 Agnès Bombrun Carboline derivatives as cgmp phosphodiesterase inhibitors
CN1326450A (en) 1998-09-24 2001-12-12 三菱化学株式会社 Hydroxyflavone derivatives as tau protein kinase inhibitors
AR023052A1 (en) 1998-09-25 2002-09-04 Mitsuharu Yoshimura Milton DERIVATIVES OF PIRIMIDONA
ATE284387T1 (en) 1998-10-08 2004-12-15 Smithkline Beecham Plc 3-(3-CHLORO-4-HYDROXYPHENYLAMINO)-4-(2-NITROPHENYL)-1H-PYRROL-2,5-DIONE AS A GLYCOGEN SYNTHASE KINASE-3 INHIBITOR (GSK-3)
US6719520B2 (en) 1998-10-08 2004-04-13 Smithkline Beecham Corporation Method and compounds
WO2000023449A1 (en) 1998-10-16 2000-04-27 Merck Sharp & Dohme Limited Pyrazolo-triazine derivatives as ligands for gaba receptors
DE19850701A1 (en) 1998-11-04 2000-05-11 Merck Patent Gmbh Benzoyl pyridazines
EP1129094A2 (en) 1998-11-12 2001-09-05 Merck & Co., Inc. Therapeutic polymorphs of a gaba-a alpha-5 inverse agonist and pamoate formulations of the same
PE20001236A1 (en) 1998-11-13 2000-11-10 Lilly Co Eli EXCITING AMINO ACID RECEIVER MODULATORS
SE9804064D0 (en) 1998-11-25 1998-11-25 A & Science Invest Ab Medicinal product and method of treatment of conditions affecting neural stem cells or progenitor cells
US6130333A (en) 1998-11-27 2000-10-10 Monsanto Company Bicyclic imidazolyl derivatives as phosphodiesterase inhibitors, pharmaceutical compositions and method of use
WO2000037471A1 (en) 1998-12-23 2000-06-29 Neurogen Corporation 2-amino-9-alkylpurines: gaba brain receptor ligands
GB9828640D0 (en) 1998-12-23 1999-02-17 Smithkline Beecham Plc Novel method and compounds
CA2357950C (en) 1998-12-30 2013-07-23 Oligo Therapeutics Inc. Therapeutic phosphodiesterase inhibitors
DE60016566T2 (en) 1999-01-27 2005-12-15 Merck Sharp & Dohme Ltd., Hoddesdon TRIAZOLOPYRIDAZINE DERIVATIVES AS LIGANDS FOR GABA RECEPTORS
US6342496B1 (en) 1999-03-01 2002-01-29 Sepracor Inc. Bupropion metabolites and methods of use
US6498176B1 (en) 1999-03-04 2002-12-24 Smithklinebeecham Corporation 3-(anilinomethylene) oxindoles as protein tyrosine kinase and protein serine/threonine kinase inhibitors
TW575561B (en) 1999-03-25 2004-02-11 Hoffmann La Roche 1-arenesulfonyl-2-aryl-pyrrolidine and piperidine derivatives
DE19915365A1 (en) 1999-04-06 2000-10-12 Merck Patent Gmbh Tetrahydropyridazine derivatives
US6528499B1 (en) 2000-04-27 2003-03-04 Georgetown University Ligands for metabotropic glutamate receptors and inhibitors of NAALADase
JP5095050B2 (en) 1999-04-28 2012-12-12 ジョージタウン ユニバーシティー Metabotropic glutamate receptor ligand and NAALADase inhibitor
FR2792938B1 (en) 1999-04-28 2001-07-06 Warner Lambert Co NEWS 1-AMINO TRIAZOLO [4,3-a] QUINAZOLINE-5-ONES PHOSPHODIESTERASE IV INHIBITORS
US6943166B1 (en) 1999-04-30 2005-09-13 Lilly Icos Llc. Compositions comprising phosphodiesterase inhabitors for the treatment of sexual disfunction
US6316472B1 (en) 1999-05-13 2001-11-13 Merck Frosst Canada & Co. Heterosubstituted pyridine derivatives as PDE 4 inhibitors
WO2000071528A1 (en) 1999-05-25 2000-11-30 Neurogen Corporation 4h-1,4-benzothiazine-2-carboxamides and their use as gaba brain receptor ligands
EP1189873A1 (en) 1999-06-03 2002-03-27 Lilly, S.A. Excitatory amino acid receptor modulators
EP1186615A4 (en) 1999-06-10 2006-05-03 Takeda Pharmaceutical Novel protein and dna thereof
US6146876A (en) 1999-06-11 2000-11-14 Millennium Pharmaceuticals, Inc. 22025, a novel human cyclic nucleotide phosphodiesterase
US6297256B1 (en) 1999-06-15 2001-10-02 Neurogen Corporation Aryl and heteroaryl substituted pyridino derivatives GABA brain receptor ligands
DE19928146A1 (en) 1999-06-19 2000-12-21 Merck Patent Gmbh New 3-benzylamino-benzothienopyrimidine derivatives inhibit phosphodiesterase V and are useful for treating cardiac insufficiency and impotence
FR2795724B1 (en) 1999-07-02 2002-12-13 Sanofi Synthelabo NOVEL BENZENE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
HUP0202186A3 (en) 1999-07-21 2003-02-28 Fujisawa Pharmaceutical Co Benzimidazolone derivatives, process for their preparation, pharmaceutical compositions containing them and their use as phosphodiesterase inhibitors for producing pharmaceutical compositions
GB9918180D0 (en) 1999-08-02 1999-10-06 Smithkline Beecham Plc Novel compositions
US6821975B1 (en) 1999-08-03 2004-11-23 Lilly Icos Llc Beta-carboline drug products
US20050137206A1 (en) 1999-08-05 2005-06-23 Yevich Joseph P. Method for treatment of anxiety and depression
DE60006618T2 (en) 1999-08-06 2004-09-23 F. Hoffmann-La Roche Ag Tetrahydrobenzo (d) azepines and their use as metabotropic glutamate receptor antagonists
US6476019B1 (en) 1999-08-13 2002-11-05 Sepracor Inc. Spirocyclic ligands for sigma receptors, and libraries and methods of use thereof
US6660753B2 (en) 1999-08-19 2003-12-09 Nps Pharmaceuticals, Inc. Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists
US6313159B1 (en) 1999-08-20 2001-11-06 Guilford Pharmaceuticals Inc. Metabotropic glutamate receptor ligand derivatives as naaladase inhibitors
GB9919957D0 (en) 1999-08-23 1999-10-27 Merck Sharp & Dohme Therapeutic agents
EP1212330B1 (en) 1999-08-27 2006-04-19 Ligand Pharmaceuticals Incorporated Androgen receptor modulator compounds and methods
JP2003508397A (en) 1999-08-27 2003-03-04 リガンド・ファーマシューティカルズ・インコーポレイテッド 8-Substituted-6-trifluoromethyl-9-pyrido [3,2-G] quinoline compounds as androgen receptor modulators
US6566372B1 (en) 1999-08-27 2003-05-20 Ligand Pharmaceuticals Incorporated Bicyclic androgen and progesterone receptor modulator compounds and methods
US6956049B1 (en) 1999-08-31 2005-10-18 Merck & Co., Inc. Methods of modulating processes mediated by excitatory amino acid receptors
GB9921150D0 (en) 1999-09-07 1999-11-10 Merck Sharp & Dohme Therapeutic agents
GB9921351D0 (en) 1999-09-09 1999-11-10 Merck Sharp & Dohme Therapeutic agents
AU767558B2 (en) 1999-09-16 2003-11-13 Mitsubishi Tanabe Pharma Corporation Aromatic nitrogenous six-membered ring compounds
TWI265925B (en) 1999-10-11 2006-11-11 Pfizer Pyrazolo[4,3-d]pyrimidin-7-ones useful in inhibiting type 5 cyclic guanosine 3',5'-monophosphate phosphodiesterases(cGMP PDE5), process and intermediates for their preparation, their uses and composition comprising them
US6552016B1 (en) 1999-10-14 2003-04-22 Curis, Inc. Mediators of hedgehog signaling pathways, compositions and uses related thereto
PL357433A1 (en) 1999-10-15 2004-07-26 F.Hoffmann-La Roche Ag Benzodiazepine derivatives as metabotropic glutamate receptor antagonists
US7491742B2 (en) 1999-10-21 2009-02-17 Merck Patent Gmbh Imidazole derivatives as phosphodiesterase VII inhibitors
US6534287B1 (en) 1999-10-25 2003-03-18 Nps Pharmaceuticals, Inc. Human metabotropic glutamate receptor
AR029185A1 (en) 1999-10-25 2003-06-18 Yamanouchi Pharma Co Ltd NAFTIRIDINE DERIVATIVE
DE19953025A1 (en) 1999-11-04 2001-05-10 Merck Patent Gmbh Pyrrole derivatives as phosphodiesterase VII inhibitors
DE19953414A1 (en) 1999-11-06 2001-05-10 Merck Patent Gmbh Imidazopyridine derivatives as phosphodiesterase VII inhibitors
DE19954707A1 (en) 1999-11-13 2001-05-17 Merck Patent Gmbh Imidazole compounds as phosphodiesterase VII inhibitors
PT1233958E (en) 1999-11-23 2011-09-20 Methylgene Inc Inhibitors of histone deacetylase
FR2801216A1 (en) 1999-11-23 2001-05-25 Centre Nat Rech Scient Use of indirubine derivatives to inhibit 3 beta-glycogen synthase kinase, for the treatment of diabetes, neurodegenerative disorders, manic-depressive disorders, cancers, or parasites
GB9927687D0 (en) 1999-11-23 2000-01-19 Merck Sharp & Dohme Therapeutic agents
EP1106180B1 (en) 1999-12-08 2003-11-12 Centre National de la Recherche Scientifique (CNRS) Use of hymenialdisine or derivatives thereof in the manufacture of medicaments
DE60008917T2 (en) 1999-12-08 2005-03-10 Grelan Pharmaceutical Co., Ltd., Hamura NEW 1,8-NAPHTYRIDINE-2 (1H) -ONE DERIVATIVES
WO2001042224A1 (en) 1999-12-09 2001-06-14 Mitsubishi Pharma Corporation Carboxyamido derivatives
US6680336B2 (en) 1999-12-15 2004-01-20 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
GB9929685D0 (en) 1999-12-15 2000-02-09 Merck Sharp & Dohme Therapeutic agents
GB9929687D0 (en) 1999-12-15 2000-02-09 Merck Sharp & Dohme Therapeutic agents
US6376489B1 (en) 1999-12-23 2002-04-23 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
WO2001044206A1 (en) 1999-12-17 2001-06-21 Chiron Corporation Pyrazine based inhibitors of glycogen synthase kinase 3
KR100711817B1 (en) 1999-12-17 2007-05-02 노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 Bicyclic inhibitors of glycogen synthase kinase 3
US7332317B2 (en) 1999-12-22 2008-02-19 Tanabe Seiyaku Co., Ltd. Phosphodiesterase and genes thereof
US6372777B1 (en) 1999-12-23 2002-04-16 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6362213B1 (en) 1999-12-23 2002-03-26 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6294561B1 (en) 1999-12-23 2001-09-25 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6258833B1 (en) 1999-12-23 2001-07-10 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6313156B1 (en) 1999-12-23 2001-11-06 Icos Corporation Thiazole compounds as cyclic-AMP-specific phosphodiesterase inhibitors
US6569885B1 (en) 1999-12-23 2003-05-27 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6348602B1 (en) 1999-12-23 2002-02-19 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
GB0000564D0 (en) 2000-01-11 2000-03-01 Merck Sharp & Dohme Therapeutic agents
EA005028B1 (en) 2000-01-31 2004-10-28 Пфайзер Продактс Инк. Pyrimidine carboxamides useful as inhibitors of pde4 isozymes
WO2001057060A1 (en) 2000-02-01 2001-08-09 Human Genome Sciences, Inc. Bcl-2-like polynucleotides, polypeptides, and antibodies
US6800651B2 (en) 2000-02-03 2004-10-05 Eli Lilly And Company Potentiators of glutamate receptors
US20010039275A1 (en) 2000-02-04 2001-11-08 Bowler Andrew Neil Use of 2,4-diaminothiazole derivatives
AU2001230026A1 (en) 2000-02-04 2001-08-14 Novo-Nordisk A/S 2,4-diaminothiazole derivatives
GB0003254D0 (en) 2000-02-11 2000-04-05 Darwin Discovery Ltd Heterocyclic compounds and their therapeutic use
FR2804959B1 (en) 2000-02-15 2006-04-28 Centre Nat Rech Scient USE OF PAULLON DERIVATIVES FOR THE MANUFACTURE OF MEDICAMENTS
DK1260512T3 (en) 2000-02-29 2007-11-05 Mitsubishi Pharma Corp Hitherto unknown cyclic amide derivatives
GB0005700D0 (en) 2000-03-09 2000-05-03 Glaxo Group Ltd Therapy
WO2001068600A2 (en) 2000-03-16 2001-09-20 Inflazyme Pharmaceuticals Limited Benzylated pde4 inhibitors
CA2404226A1 (en) 2000-03-23 2001-09-27 Takeda Chemical Industries, Ltd. Furoisoquinoline derivatives, process for producing the same and use thereof
EP1136482A1 (en) 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-Amino-3-(alkyl)-pyrimidone derivatives as GSK3beta inhibitors
EP1136485A1 (en) 2000-03-23 2001-09-26 Sanofi-Synthelabo Aminophenyl pyrimidone derivatives
AU2001248365A1 (en) 2000-03-23 2001-10-03 Mitsubishi Pharma Corporation 2-(arylalkylamino)pyrimidone derivatives and 2-(heteroarylalkylamino)pyrimidone derivatives
EP1136486A1 (en) 2000-03-23 2001-09-26 Sanofi-Synthelabo 2-[Indanylamino]pyrimidone and 2-[tetrahydronaphthalenylamino]pyrimidone derivatives
AU2001262150A1 (en) 2000-03-23 2001-10-03 Mitsubishi Pharma Corporation 2-(nitrogen-heterocyclic)pyrimidone derivatives
WO2001070243A2 (en) 2000-03-23 2001-09-27 Nexell Therapeutics Inc. A method for treating early breast cancer
JP2005289808A (en) 2000-03-23 2005-10-20 Sanofi-Aventis 3-substituted-4-pyrimidone derivative
ATE489360T1 (en) 2000-03-24 2010-12-15 Methylgene Inc HISTONE DEACETYLASE INHIBITORS
GB0007193D0 (en) 2000-03-25 2000-05-17 Univ Manchester Treatment of movrmrnt disorders
US6683192B2 (en) 2000-03-30 2004-01-27 Curis, Inc. Small organic molecule regulators of cell proliferation
GB0007842D0 (en) 2000-03-31 2000-05-17 Spruce Barbara Sigma receptor ligands and their medical uses
US6761987B2 (en) 2000-03-31 2004-07-13 Plug Power Inc. Fuel cell system having an energy source backup
GB0008264D0 (en) 2000-04-04 2000-05-24 Smithkline Beecham Plc Novel method and compounds
GB0008696D0 (en) 2000-04-07 2000-05-31 Merck Sharp & Dohme Therapeutic agents
WO2001076507A2 (en) 2000-04-11 2001-10-18 The University Of Miami Use of oxygen carriers to improve grafted cell survival in neural transplantation
DE60139550D1 (en) 2000-04-14 2009-09-24 Mars Inc COMPOSITIONS AND METHODS FOR IMPROVING VACCULAR HEALTH
CA2306170A1 (en) 2000-04-18 2001-10-18 Kenneth Curry Novel amino, carboxy derivatives of barbituric acid
WO2001081345A1 (en) 2000-04-20 2001-11-01 Mitsubishi Pharma Corporation Aromatic amide compounds
WO2001085669A1 (en) 2000-05-11 2001-11-15 Kenneth Curry Novel spiro[2.4]heptane amino carboxy compounds and derivatives thereof
CZ296087B6 (en) 2000-05-11 2006-01-11 Consejo Superior Investigaciones Cientificas Pharmaceutical composition intended for the treatment of a disease in which heterocyclic inhibitors of glycogen synthase kinase GSK-3 are involved
UA74826C2 (en) 2000-05-17 2006-02-15 Ortho Mcneil Pharm Inc ?-carboline derivatives as phosphodiesterase inhibitors
UA72611C2 (en) 2000-05-17 2005-03-15 Орто-Макнейл Фармацевтикал, Інк. Derivatives of substituted pyrrolopyridinone useful as phosphodiesterase inhibitors
EP1294723A1 (en) 2000-05-24 2003-03-26 MERCK SHARP &amp; DOHME LTD. 3-phenyl-imidazo-pyrimidine derivatives as ligands for gaba receptors
ATE324800T1 (en) 2000-05-30 2006-06-15 Nestle Sa PRIMARY COMPOSITION CONTAINING A LIPOPHILIC BIOACTIVE SUBSTANCE
US7081481B2 (en) 2000-05-31 2006-07-25 Eli Lilly And Company Excitatory amino acid receptor modulators
ES2222389T3 (en) 2000-06-07 2005-02-01 Almirall Prodesfarma, S.A. DERIVATIVES OF 6-PHENYLPIRROLOPIRIMIDINDIONA.
ATE333457T1 (en) 2000-06-23 2006-08-15 Lilly Icos Llc CYCLIC GMP-SPECIFIC PHOSPHODIESTERASE INHIBITORS
US6589978B2 (en) 2000-06-30 2003-07-08 Hoffman-La Roche Inc. 1-sulfonyl pyrrolidine derivatives
US6399641B1 (en) 2000-07-13 2002-06-04 Hoffmann-La Roche Inc. 2H-tetrazole-amide compounds with therapeutic activity as metabotropic glutamate receptor agonists
GB0018473D0 (en) 2000-07-27 2000-09-13 Merck Sharp & Dohme Therapeutic agents
BR0112965A (en) 2000-07-27 2003-07-08 Hoffmann La Roche 3-Indolyl-4-phenyl-1h-pyrrol-2,5-dione derivatives as glocogen synthase kinase-3beta inhibitors
GT200100147A (en) 2000-07-31 2002-06-25 IMIDAZOL DERIVATIVES
WO2002009713A2 (en) 2000-08-01 2002-02-07 Bayer Aktiengesellschaft Selective pde 2 inhibitors, used as medicaments for improving cognition
US6645990B2 (en) 2000-08-15 2003-11-11 Amgen Inc. Thiazolyl urea compounds and methods of uses
IL154016A0 (en) 2000-08-31 2003-07-31 Pfizer Prod Inc Pyrazole derivatives and their use as protein kinase inhibitors
AR030587A1 (en) 2000-09-01 2003-08-27 Sanofi Aventis DERIVATIVES OF 2-PIRIDINIL-6,7,8,9-TETRAHYDROPIRIMIDO [1,2-A] PIRIMIDIN-4-ONA AND 7-PIRIDINIL-2,3-DIHYDROIMIDAZO [1,2-A] PIRIMIDIN-5 (1H) -ONA
PE20020354A1 (en) 2000-09-01 2002-06-12 Novartis Ag HYDROXAMATE COMPOUNDS AS HISTONE-DESACETILASE (HDA) INHIBITORS
EP1184384A1 (en) 2000-09-01 2002-03-06 Sanofi-Synthelabo 1-(Alkyl), 1-((heteroaryl)alkyl) and 1-((aryl)alkyl)-7-pyridin-4-ylimidazo(1,2a)pyrimidin-5(1H)-one derivatives
US6576644B2 (en) 2000-09-06 2003-06-10 Bristol-Myers Squibb Co. Quinoline inhibitors of cGMP phosphodiesterase
EP1317433A2 (en) 2000-09-06 2003-06-11 Chiron Corporation Inhibitors of glycogen synthase kinase 3
AU2001288972A1 (en) 2000-09-11 2002-03-26 Sepracor, Inc. Antipsychotic sulfonamide-heterocycles, and methods of use thereof
US6610677B2 (en) 2000-09-15 2003-08-26 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
AU2001291013A1 (en) 2000-09-15 2002-03-26 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US6613776B2 (en) 2000-09-15 2003-09-02 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US20040115309A1 (en) 2000-09-22 2004-06-17 Harris Patricia Anna Food supplement
JP4975941B2 (en) 2000-09-29 2012-07-11 トポターゲット ユーケー リミテッド (E) -N-hydroxy-3- (3-sulfamoyl-phenyl) acrylamide compound and therapeutic use thereof
GB0023983D0 (en) 2000-09-29 2000-11-15 Prolifix Ltd Therapeutic compounds
US7569724B2 (en) 2000-09-29 2009-08-04 Topotarget Uk Limited Carbamic acid compounds comprising an amide linkage as HDAC inhibitors
JP3830746B2 (en) 2000-09-29 2006-10-11 スガツネ工業株式会社 Hinge device
EP1193261A1 (en) 2000-10-02 2002-04-03 Warner-Lambert Company New thiadiazoles and their use as phosphodiesterase-7 inhibitors
BR0114253A (en) 2000-10-02 2003-07-01 Janssen Pharmaceutica Nv Metabotropic Glutamate Receptor Antagonists
AU2002210385A1 (en) 2000-10-16 2002-04-29 Novo-Nordisk A/S Furazanyl-triazole derivates for the treatment of diseases
US20020103192A1 (en) 2000-10-26 2002-08-01 Curtin Michael L. Inhibitors of histone deacetylase
GB0117277D0 (en) 2001-07-16 2001-09-05 Merck Sharp & Dohme Therapeutic agents
AU2002212530B2 (en) 2000-11-10 2006-08-17 Merck Sharp & Dohme Limited Imidazo-triazine derivatives as ligands for GABA receptors
GB0027561D0 (en) 2000-11-10 2000-12-27 Merck Sharp & Dohme Therapeutic agents
AU2954102A (en) 2000-11-14 2002-05-27 Byk Gulden Lomberg Chem Fab (dihydro)isoquinoline derivatives as phosphodiesterase inhibitors
AR035659A1 (en) 2000-12-07 2004-06-23 Hoffmann La Roche HYDROXYAMIDES OF ACID (1-OXO-1,2,3,4-TETRAHIDRO-NAFTALEN-2-IL) -ALCANOICO, PROCESS FOR THE MANUFACTURE OF THESE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS AND USES OF THE SAME
CA2431326A1 (en) 2000-12-13 2002-06-20 Bayer Aktiengesellschaft Pyrrolo (2.1-a) dihydroisoquinolines and their use as phosphodiesterase 10a inhibitors
US6900215B2 (en) 2000-12-15 2005-05-31 Merck Sharp & Dohme Ltd. Imidazo-pyrimidine derivatives as ligands for gaba receptors
US6562995B1 (en) 2000-12-21 2003-05-13 Beacon Laboratories, Inc. Delta dicarbonyl compounds and methods for using the same
AU2001297619B2 (en) 2000-12-21 2006-06-08 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US6720445B2 (en) 2000-12-21 2004-04-13 Beacon Laboratories, Inc. Acetyloxymethyl esters and methods for using the same
ATE297734T1 (en) 2000-12-22 2005-07-15 Hoffmann La Roche TETRAHYDRO-(BENZO- OR THIENO-)AZEPINE-PYRAZINE AND TRIAZINE DERIVATIVES AS MGLUR 1 ANTAGONISTS
AR035513A1 (en) 2000-12-23 2004-06-02 Hoffmann La Roche DERIVATIVES OF TETRAHYDROPIRIDINE, PROCESS TO PREPARE THEM, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND USE OF SUCH COMPOUNDS IN THE PREPARATION OF MEDICINES
US6974824B2 (en) 2001-01-08 2005-12-13 Research Triangle Institute Kappa opioid receptor ligands
AR035417A1 (en) 2001-01-27 2004-05-26 Hoffmann La Roche TRICYCLE DERIVATIVES OF LACTAMA AND SULTAMA, PROCESSES FOR THEIR DEVELOPMENT, DRUGS THAT CONTAIN THEM, AND THE USE OF SUCH COMPOUNDS IN THE PREPARATION OF DRUGS
IL156413A0 (en) 2001-01-31 2004-01-04 Pfizer Prod Inc Nicotinamide biaryl derivatives useful as inhibitors of pde4 isozymes
SK8942003A3 (en) 2001-01-31 2004-10-05 Pfizer Prod Inc Ether derivatives useful as inhibitors
KR20030072614A (en) 2001-01-31 2003-09-15 화이자 프로덕츠 인크. Thiazolyl-, Oxazolyl-, Pyrrolyl-, and Imidazolyl-Acid Amide Derivatives Useful as Inhibitors of PDE4 Isozymes
US6559159B2 (en) 2001-02-01 2003-05-06 Research Triangle Institute Kappa opioid receptor ligands
US6617357B2 (en) 2001-03-06 2003-09-09 Smithkline Beecham Corporation Compounds and their use as PDE inhibitors
US20020177594A1 (en) 2001-03-14 2002-11-28 Curtin Michael L. Inhibitors of histone deacetylase
AP1699A (en) 2001-03-21 2006-12-26 Warner Lambert Co New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors
US6900329B2 (en) 2001-03-21 2005-05-31 Schering Corporation MCH antagonists and their use in the treatment of obesity
WO2002088079A2 (en) 2001-05-01 2002-11-07 Bristol-Myers Squibb Company Dual inhibitors of pde 7 and pde 4
US20030187027A1 (en) 2001-05-09 2003-10-02 Schreiber Stuart L. Dioxanes and uses thereof
ATE347361T1 (en) 2001-05-25 2006-12-15 Boehringer Ingelheim Pharma COMBINATION OF A PDE4 INHIBITOR WITH TIOTROPIUM FOR THE TREATMENT OF OBSTRUCTIVE AIRWAY DISEASES
NZ529335A (en) 2001-05-25 2005-09-30 Pfizer A PDE 4 inhibitor and an anti-cholinergic agent in combination for treating obstructive airways diseases
MXPA03010961A (en) 2001-05-31 2004-02-27 Vertex Pharma Thiazole compounds useful as inhibitors of protein kinases.
RU2003137766A (en) 2001-06-12 2005-05-20 Ск Корпорейшн (Kr) NEW Phenylalkyl analogues of diamines and amides
PE20030008A1 (en) 2001-06-19 2003-01-22 Bristol Myers Squibb Co DUAL INHIBITORS OF PDE 7 AND PDE 4
WO2002102313A2 (en) 2001-06-19 2002-12-27 Bristol-Myers Squibb Company Pyrimidine inhibitors of phosphodiesterase (pde) 7
DE10130167A1 (en) 2001-06-22 2003-01-02 Bayer Ag imidazotriazines
SE0102440D0 (en) 2001-07-05 2001-07-05 Astrazeneca Ab New compound
JP2003029331A (en) 2001-07-13 2003-01-29 Sano Fuji Koki Co Ltd Reflection type liquid-crystal projector
US6821976B2 (en) 2001-07-24 2004-11-23 Bristol-Myers Squibb Company S-6-hydroxy-buspirone
WO2003011843A1 (en) 2001-08-03 2003-02-13 Novo Nordisk A/S Novel 2,4-diaminothiazole derivatives
EP1285922A1 (en) 2001-08-13 2003-02-26 Warner-Lambert Company 1-Alkyl or 1-cycloalkyltriazolo[4,3-a]quinazolin-5-ones as phosphodiesterase inhibitors
JO2311B1 (en) 2001-08-29 2005-09-12 ميرك فروست كندا ليمتد Alkyne-aryl phosphodiesterase-4 inhibitors
KR20040048411A (en) 2001-09-14 2004-06-09 메틸진, 인크. Inhibitors of histone deacetylase
US6897220B2 (en) 2001-09-14 2005-05-24 Methylgene, Inc. Inhibitors of histone deacetylase
DE60227718D1 (en) 2001-09-21 2008-08-28 Sanofi Aventis Use of 2-fuoro-3-ketoesters for the preparation of 3-fuoro-6,7,8,9-tetrahydro-4H-pyrimido-1,2-a-pyrimidin-4-ones
EP1295885A1 (en) 2001-09-21 2003-03-26 Sanofi-Synthelabo Substituted 2-pyridinyl-6,7,8,9-tetrahydropyrimido(1,2-a)pyrimidin-4-one and 7-pyridinyl-2,3-dihydroimidazo(1,2-a)pyrimidin-5(1H)one derivatives
KR100868840B1 (en) 2001-09-21 2008-11-14 사노피-아벤티스 Substituted 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyrimidinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-51hone derivatives for neurodegenerative disorders
EP1295884A1 (en) 2001-09-21 2003-03-26 Sanofi-Synthelabo 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]Pyrimidin-4-one and 7-Pyrimidinyl-2,3-Dihydroimidazo[1,2-a]Pyrimidin-5(1H)one derivatives
DE10148618B4 (en) 2001-09-25 2007-05-03 Schering Ag Substituted N- (1,4,5,6-tetrahydro-cyclopentapyrazol-3-yl) derivatives, their preparation and use as medicaments
US6900205B2 (en) 2001-09-26 2005-05-31 Bayer Pharmaceuticals Corporation 1,8-Naphthyridine derivatives and their use to treat diabetes and related disorders
US6951849B2 (en) 2001-10-02 2005-10-04 Acadia Pharmaceuticals Inc. Benzimidazolidinone derivatives as muscarinic agents
NZ531550A (en) 2001-10-02 2006-12-22 Acadia Pharm Inc Benzimidazolidinone derivatives as muscarinic cholinergic receptors
WO2004089942A2 (en) 2001-10-02 2004-10-21 Acadia Pharmaceuticals Inc. Benzimidazolidinone derivatives as muscarinic agents
US7029163B2 (en) 2002-10-07 2006-04-18 Advanced Biomaterial Systems, Inc. Apparatus for mixing and dispensing components
US6924311B2 (en) 2001-10-17 2005-08-02 X-Ceptor Therapeutics, Inc. Methods for affecting various diseases utilizing LXR compounds
IL161041A0 (en) 2001-10-25 2004-08-31 Schering Corp Mch antagonists for the treatment of obesity
CN100436427C (en) 2001-11-01 2008-11-26 詹森药业有限公司 Aminobenzamide derivatives as glycogen synthase kinase 3 beta inhibitors
MXPA04004178A (en) 2001-11-01 2004-09-06 Janssen Pharmaceutica Nv Heteroaryl amines as glycogen synthase kinase 3beta inhibitors (gsk3 inhibitors).
JP2005507419A (en) 2001-11-01 2005-03-17 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ Amide derivatives as glycogen synthase kinase 3 beta inhibitors
CN1280292C (en) 2001-11-14 2006-10-18 奥索-麦克尼尔药品公司 Substituted tetracyclic pyrroloquinolone derivatives useful as phosphodiesterase inhibitors
GB0128287D0 (en) 2001-11-26 2002-01-16 Smithkline Beecham Plc Novel method and compounds
FR2832711B1 (en) 2001-11-26 2004-01-30 Warner Lambert Co TRIAZOLO [4,3-A] PYRIDO [2,3-D] PYRIMIDIN-5-ONES DERIVATIVES, COMPOSITIONS CONTAINING SAME, PROCESS FOR PREPARATION AND USE
WO2003048137A1 (en) 2001-11-30 2003-06-12 Merck & Co., Inc. Metabotropic glutamate receptor-5 modulators
BR0207215A (en) 2001-12-13 2004-02-10 Daiichi Suntory Pharma Co Ltd Pyrazolopyriminone derivatives having pde7 inhibition action
US7569592B2 (en) 2001-12-18 2009-08-04 Merck & Co., Inc. Heteroaryl substituted pyrazole modulators of metabotropic glutamate receptor-5
ES2292854T3 (en) 2001-12-18 2008-03-16 MERCK &amp; CO., INC. TRIAZOL MODULATORS REPLACED WITH METABOTROPIC GLUMATAMATE RECEIVER-5 HETEROARILE.
AU2002360621B2 (en) 2001-12-19 2007-01-25 Merck & Co., Inc. heteroaryl substituted imidazole modulators of metabotropic glutamate receptor-5
WO2003051847A1 (en) 2001-12-19 2003-06-26 Smithkline Beecham P.L.C. (1-h-indazol-3-yl) -amide derivatives as gsk-3 inhibitors
SE0104341D0 (en) 2001-12-20 2001-12-20 Astrazeneca Ab New use
SE0104340D0 (en) 2001-12-20 2001-12-20 Astrazeneca Ab New compounds
CA2470519C (en) 2001-12-21 2009-11-17 Merck & Co., Inc. Heteroaryl substituted pyrrole modulators of metabotropic glutamate receptor-5
TW200301123A (en) 2001-12-21 2003-07-01 Astrazeneca Uk Ltd New use
EP1458711B1 (en) 2001-12-21 2007-07-18 AstraZeneca AB Use of oxindole derivatives in the treatment of dementia related diseases, alzheimer s disease and conditions associated with glycogen synthase kinase-3
DE10163991A1 (en) 2001-12-24 2003-07-03 Merck Patent Gmbh Pyrrolo-pyrimidine
KR100897970B1 (en) 2001-12-27 2009-05-18 다이쇼 세이야꾸 가부시끼가이샤 6-Fluorobicyclo[3.1.0]hexane Derivatives
US7550459B2 (en) 2001-12-28 2009-06-23 Acadia Pharmaceuticals, Inc. Tetrahydroquinoline analogues as muscarinic agonists
CN101050215A (en) 2001-12-28 2007-10-10 阿卡蒂亚药品公司 Spiroazacyclic compounds as monoamine receptor modulators
ES2251624T3 (en) 2001-12-28 2006-05-01 Acadia Pharmaceuticals Inc. ANALOGS OF TETRAHYDROQUINOLINE AS MUSCARINIC AGONISTS.
EP1468684A4 (en) 2002-01-22 2008-02-27 Eisai R&D Man Co Ltd Sigma receptor binder containing indanone derivative
WO2003064389A1 (en) 2002-01-31 2003-08-07 Ono Pharmaceutical Co., Ltd. Nitrogen-containing bicyclic compounds and drugs containing the same as the active ingredient
MXPA04007737A (en) 2002-02-11 2004-10-15 Pfizer Nicotinamide derivatives useful as pde4 inhibitors.
AU2003245700A1 (en) 2002-02-12 2003-09-04 Glaxo Group Limited Pyrazolopyridine derivatives
KR20040086428A (en) 2002-02-22 2004-10-08 데이진 가부시키가이샤 Pyrrolopyrimidine derivative
TW200306191A (en) 2002-02-22 2003-11-16 Teijin Ltd Pyrrolopyrimidine derivatives
DE60302221T2 (en) 2002-02-28 2006-08-03 Sanofi-Aventis HETEROARYL SUBSTITUTED 2-PYRIDINYL AND 2-PYRIMIDINYL-6,7,8,9-TETRAHYDROPYRIMIDO [1,2-A] PYRIMIDIN-4-ONDERIVATE
EP1340759A1 (en) 2002-02-28 2003-09-03 Sanofi-Synthelabo 1-[alkyl], 1-[(heteroaryl)alkyl] and 1-[(aryl)alkyl]-7-(pyrimidin-4-yl)-imidazo[1,2-a]pyrimidin-5(1H)-one derivatives
DE60309848T2 (en) 2002-03-05 2007-05-16 Eli Lilly And Co., Indianapolis Purine derivatives as kinase inhibitors
MXPA04008671A (en) 2002-03-08 2004-12-06 Lilly Co Eli Pyrrole-2, 5-dione derivatives and their use as gsk-3 inhibitors.
WO2003076437A1 (en) 2002-03-11 2003-09-18 Schering Aktiengesellschaft Cdk inhibiting 2-heteroaryl pyrimidine, the production thereof, and use thereof as a medicament
WO2003077918A1 (en) 2002-03-12 2003-09-25 Merck & Co., Inc. Di-aryl substituted tetrazole modulators of metabotropic glutamate receptor-5
KR20040093692A (en) 2002-03-13 2004-11-08 얀센 파마슈티카 엔.브이. Piperazinyl-, piperidynyl- and morpholinyl-derivatives as novel inhibitors of histone deacetylase
US7501417B2 (en) 2002-03-13 2009-03-10 Janssen Pharmaceutica, N.V. Aminocarbonyl-derivatives as novel inhibitors of histone deacetylase
DK1485365T3 (en) 2002-03-13 2008-09-01 Janssen Pharmaceutica Nv Sulfonyl derivatives as novel inhibitors of histane deacetylase
JP4725945B2 (en) 2002-03-13 2011-07-13 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ Sulfonylamino derivatives as novel inhibitors of histone deacetylase
DE60220016T2 (en) 2002-03-20 2008-01-10 Société des Produits Nestlé S.A. Cocoa extract with low fat content
US7514107B2 (en) 2002-03-21 2009-04-07 Mars, Incorporated Treatment of diseases involving defective gap junctional communication
GB0206723D0 (en) 2002-03-21 2002-05-01 Glaxo Group Ltd Novel compounds
GB0207249D0 (en) 2002-03-27 2002-05-08 Glaxo Group Ltd Novel compounds
GB0207246D0 (en) 2002-03-27 2002-05-08 Glaxo Group Ltd Novel compounds
SE0302546D0 (en) 2003-09-24 2003-09-24 Astrazeneca Ab New compounds
SE0200979D0 (en) 2002-03-28 2002-03-28 Astrazeneca Ab New compounds
ES2309313T3 (en) 2002-04-03 2008-12-16 Topotarget Uk Limited CARBAMIC ACID COMPOUNDS THAT INCLUDE A COUPLING OF PIPERACINE AS HDAC INHIBITORS.
PE20040079A1 (en) 2002-04-03 2004-04-19 Novartis Ag INDOLYLMALEIMIDE DERIVATIVES
SE0201194D0 (en) 2002-04-19 2002-04-19 Astrazeneca Ab New compounds
ES2300573T3 (en) 2002-05-08 2008-06-16 Janssen Pharmaceutica Nv KINASE INHIBITORS REPLACED WITH PIRROLINA.
KR20050008787A (en) 2002-06-05 2005-01-21 얀센 파마슈티카 엔.브이. Bisindolyl-maleimid derivatives as kinase inhibitors
ATE409035T1 (en) 2002-06-05 2008-10-15 Janssen Pharmaceutica Nv SUBSTITUTED PYRROLINES AS KINASE INHIBITORS
SI1534707T1 (en) 2002-06-19 2008-04-30 Janssen Pharmaceutica Nv Substituted 2,4-dihydro-pyrrolo (3, 4-b) -quinolin-9-one derivatives useful as phosphodiesterase inhibitors
GB0214784D0 (en) * 2002-06-26 2002-08-07 Pfizer Ltd Novel combination
SI2256108T1 (en) 2002-07-18 2016-05-31 Janssen Pharmaceutica N.V. Substituted triazine kinase inhibitors
RU2368604C2 (en) 2002-07-19 2009-09-27 Мемори Фармасьютиклз Корпорейшн Phosphodiestarase 4 inhibitors, containing n-substituted aniline and diphenylamine analogues
AU2003254053A1 (en) 2002-07-23 2004-02-09 Smithkline Beecham Corporation Pyrazolopyrimidines as protein kinase inhibitors
EP1551841A1 (en) 2002-07-23 2005-07-13 SmithKline Beecham Corporation Pyrazolopyrimidines as kinase inhibitors
US20050267133A1 (en) 2002-07-23 2005-12-01 Brown Matthew L Pyrazolopyrimidines as kinase inhibitors
CA2494100C (en) 2002-08-02 2011-10-11 Vertex Pharmaceuticals Incorporated Pyrazole compositions useful as inhibitors of gsk-3
US7277877B2 (en) 2002-08-14 2007-10-02 Sony Corporation System and method for selecting a music channel
DE10239042A1 (en) 2002-08-21 2004-03-04 Schering Ag New fused macrocyclic pyrimidine derivatives, useful as e.g. cyclin-dependent kinase inhibitors for treating e.g. cancer, autoimmune, cardiovascular or neurodegenerative diseases or viral infections
US6822418B2 (en) 2002-08-23 2004-11-23 International Rectifier Corporation Position estimation and demagnetization detection of a permanent magnet motor
KR101088922B1 (en) 2002-09-04 2011-12-01 파마코페이아, 엘엘씨. Pyrazolopyrimidines as cyclin-dependent kinase inhibitors
NZ539161A (en) 2002-09-04 2006-05-26 Schering Corp Pyrazolopyrimidines as cyclin dependent kinase inhibitors
CN1219408C (en) 2002-09-13 2005-09-14 华为技术有限公司 Juncture attaching location register and user routing information alternating method
EP1400244A1 (en) 2002-09-17 2004-03-24 Warner-Lambert Company LLC New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors
US7323334B2 (en) 2002-10-04 2008-01-29 The Regents Of The University Of California Screening and therapeutic methods relating to neurogenesis
AU2003282976A1 (en) 2002-10-21 2004-05-13 Chiron Corporation Inhibitors of glycogen synthase kinase 3
GB0226583D0 (en) 2002-11-14 2002-12-18 Cyclacel Ltd Compounds
FR2847253B1 (en) 2002-11-19 2007-05-18 Aventis Pharma Sa NOVEL DERIVATIVES OF PYRIDAZINONES AS MEDICAMENTS AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM
US6969702B2 (en) 2002-11-20 2005-11-29 Neuronova Ab Compounds and methods for increasing neurogenesis
WO2004045592A2 (en) * 2002-11-20 2004-06-03 Neuronova Ab Compounds and methods for increasing neurogenesis
ES2209650B2 (en) 2002-12-09 2006-11-01 Laboratorios Del Dr. Esteve, S.A. NON-HUMAN MAMMALS DEFICIENT MUTANTS IN SIGMA RECEIVERS AND THEIR APPLICATIONS.
AU2003293409A1 (en) 2002-12-09 2004-06-30 Karl K. Johe Method for discovering neurogenic agents
GB0229581D0 (en) 2002-12-19 2003-01-22 Cyclacel Ltd Use
US7135493B2 (en) 2003-01-13 2006-11-14 Astellas Pharma Inc. HDAC inhibitor
JP2006515013A (en) 2003-01-23 2006-05-18 クリスタルジェノミクス、インコーポレイテッド Glycogen synthase kinase 3β activity inhibitor, composition and method for producing the same
MXPA05008186A (en) 2003-01-31 2005-10-05 Astrazeneca Ab Saturated quinoxaline derivatives and their use as metabotropic glutamate receptor ligands.
US7407962B2 (en) 2003-02-07 2008-08-05 Vertex Pharmaceuticals Incorporated Heteroaryl compounds useful as inhibitors or protein kinases
GB0303319D0 (en) 2003-02-13 2003-03-19 Novartis Ag Organic compounds
EP1454910A1 (en) 2003-03-07 2004-09-08 Sanofi-Synthelabo Substituted pyrimidinyl-2-(diaza-bicyclo-alkyl)-pyrimidone derivatives
EP1454908B1 (en) 2003-03-07 2008-02-27 Sanofi-Aventis Substituted pyridinyl-2-(diaza-bicyclo-alkyl)-pyrimidinone derivatives
EP1454909B1 (en) 2003-03-07 2008-08-20 Sanofi Aventis Substituted 8'-pyridinyl-dihydrospiro-(cycloalkyl)-pyrimido(1,2-a) pyrimidin-6-one and 8'-pyrimidinyl-dihydrospiro-(cycloalkyl)-pyrimido(1,2-a)pyrimidin-6-one derivatives and their use against neurodegenerative diseases
EP1454900A1 (en) 2003-03-07 2004-09-08 Sanofi-Synthelabo Process for the preparation of pyridinyl and pyrimidinyl mono-fluorinated beta keto-esters
TWI292318B (en) 2003-03-10 2008-01-11 Hoffmann La Roche Imidazol-4-yl-ethynyl-pyridine derivatives
EP1603886B1 (en) 2003-03-12 2009-02-18 Vertex Pharmaceuticals Incorporated 4-substituted-5-cyano-1h-pyrimidin-6-(thi)ones as gsk-3 inhibitors
KR20050122210A (en) 2003-03-17 2005-12-28 다케다 샌디에고, 인코포레이티드 Histone deacetylase inhibitors
EP1460076A1 (en) 2003-03-21 2004-09-22 Sanofi-Synthelabo Substituted 8-perfluoroalkyl-6,7,8,9-tetrahydropyrimido[1,2-a] pyrimidin-4-one derivatives
JP2006521343A (en) 2003-03-27 2006-09-21 ファイザー・プロダクツ・インク Substituted 4-amino [1,2,4] triazolo [4,3-a] quinoxaline
RU2358735C2 (en) 2003-03-28 2009-06-20 Акадиа Фармасьютикалз Инк. M1 muscarine receptor agonists for analgetic therapy
US20040199842A1 (en) 2003-04-04 2004-10-07 Sartschev Ronald A. Test system with high accuracy time measurement system
ATE365554T1 (en) 2003-04-04 2007-07-15 Dynogen Pharmaceuticals Inc METHOD OF TREATING LOWER URINARY TRACT DISEASES
RU2005135330A (en) 2003-04-16 2006-06-27 Мемори Фармасьютиклз Корпорейшн (Us) PHOSPHODESTHESIS INHIBITORS 4
EP1622577A4 (en) 2003-04-17 2007-09-26 Univ Leland Stanford Junior Prevention of deficits in neurogenesis with anti-inflammatory agents
CA2524161C (en) 2003-05-08 2013-01-15 Applied Research Systems Ars Holding N.V. Pyridinyl acetonitriles
GB0311859D0 (en) 2003-05-22 2003-06-25 Merck Sharp & Dohme Therapeutic agents
WO2004106343A2 (en) 2003-05-30 2004-12-09 Ufc Limited Agelastatin derivatives of antitumour and gsk-3beta-inhibiting alkaloids
JP2007500748A (en) 2003-06-13 2007-01-18 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ Substituted indazolyl (indolyl) maleimide derivatives as kinase inhibitors
US7763588B2 (en) 2003-06-13 2010-07-27 The Salk Institute For Biological Studies Method for increasing cognitive function and neurogenesis
BRPI0411874A (en) 2003-06-23 2006-08-08 Pionner Hi Bred International plant-controlled staygreen potential by genetically engineered single gene
BRPI0411122A (en) 2003-06-27 2006-07-18 Pfizer Prod Inc pyrazol [3,4-b] pyridin-6-ones as gsk-3 inhibitors
BRPI0411891A (en) 2003-06-27 2006-08-29 Pfizer Prod Inc pyrazol [3,4-b] pyridin-6-ones as gsk-3 inhibitors
TWI372050B (en) 2003-07-03 2012-09-11 Astex Therapeutics Ltd (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles
GB0315657D0 (en) 2003-07-03 2003-08-13 Astex Technology Ltd Pharmaceutical compounds
US7842835B2 (en) 2003-07-07 2010-11-30 Georgetown University Histone deacetylase inhibitors and methods of use thereof
GB0315966D0 (en) 2003-07-08 2003-08-13 Cyclacel Ltd Compounds
KR20060120393A (en) 2003-07-16 2006-11-27 얀센 파마슈티카 엔.브이. Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors
CN100549014C (en) 2003-07-16 2009-10-14 詹森药业有限公司 Triazolopyrimidine derivative as the Glycogen Synthase kinase 3 inhibitor
KR101204247B1 (en) 2003-07-22 2012-11-22 아스텍스 테라퓨틱스 리미티드 3,4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases cdk and glycogen synthase kinase-3 gsk-3 modulators
AU2004262897B9 (en) 2003-07-25 2009-12-17 F. Hoffmann-La Roche Ag Combination of mGluR2 antagonist and ache inhibitor for treatment of acute and/or chronic neurological disorders
WO2005012262A1 (en) 2003-07-30 2005-02-10 Cyclacel Limited 2-aminophenyl-4-phenylpyrimidines as kinase inhibitors
CA2533870A1 (en) 2003-07-30 2005-02-10 Shudong Wang Pyridinylamino-pyrimidine derivatives as protein kinase inhibitors
JP2007519393A (en) 2003-08-05 2007-07-19 ユニバーシティー オブ フロリダ リサーチ ファンデーション, インク. Nervous system cell assay
AU2004265995A1 (en) 2003-08-15 2005-02-24 Blackboard Inc. Content system and associated methods
EP1661897B1 (en) 2003-08-26 2013-12-04 Teijin Pharma Limited Pyrrolopyrimidinone derivative
TWI339206B (en) 2003-09-04 2011-03-21 Vertex Pharma Compositions useful as inhibitors of protein kinases
WO2005025567A1 (en) 2003-09-12 2005-03-24 Applied Research Systems Ars Holding N.V. Benzothiazole derivatives for the treatment of diabetes
US20070185104A1 (en) 2003-09-12 2007-08-09 Applied Research Systems Ars Holding N.V. Benzoxazole acetonitriles
AU2004272306A1 (en) 2003-09-12 2005-03-24 Merck Serono Sa Benzimidazole acetonitriles
JP2007508316A (en) 2003-10-10 2007-04-05 マーズ インコーポレイテッド Treatment of diseases associated with ErbB2 kinase overexpression
ES2288270T3 (en) 2003-10-10 2008-01-01 Pfizer Products Incorporated 2H- (1,2,4) TRIAZOLO (4,3-A) REPLACED PIRAZINS AS INHIBITORS OF GSK-3.
DE10349423A1 (en) 2003-10-16 2005-06-16 Schering Ag Sulfoximine-substituted parimidines as CDK and / or VEGF inhibitors, their preparation and use as medicaments
WO2005042525A1 (en) 2003-10-21 2005-05-12 Cyclacel Limited Pyrimidin-4-yl-3, 4-thione compounds and their use in therapy
US7671072B2 (en) 2003-11-26 2010-03-02 Pfizer Inc. Aminopyrazole derivatives as GSK-3 inhibitors
US7855195B2 (en) 2003-12-02 2010-12-21 Pharmaneuroboost N.V. Method of treating mental disorders using D4 and 5-HT2A antagonists, inverse agonists or partial agonists
WO2005066151A2 (en) 2003-12-19 2005-07-21 Takeda San Diego, Inc. Histone deacetylase inhibitors
WO2005065681A1 (en) 2003-12-19 2005-07-21 Takeda San Diego, Inc. N- hydroxy-3-(3-(1h-imidazol-2-yl)-phenyl)-acrylamide derivatives and related compounds as histone deacetylase (hdac) inhibitors for the treatment of cancer
AU2004308955B2 (en) 2003-12-22 2011-08-04 Acadia Pharmaceuticals Inc. Amino substituted diaryl[a,d]cycloheptene analogs as muscarinic agonists and methods of treatment of neuropsychiatric disorders
EP1718280A4 (en) 2004-01-30 2010-08-18 Mars Inc Methods and compositions for treating cancer
TWI301760B (en) 2004-02-27 2008-10-11 Merz Pharma Gmbh & Co Kgaa Tetrahydroquinolinones and their use as antagonists of metabotropic glutamate receptors
WO2005108367A1 (en) 2004-05-03 2005-11-17 Envivo Pharmaceuticals, Inc. Compounds for treatment of neurodegenerative diseases

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004014911A1 (en) * 2002-08-08 2004-02-19 Memory Pharmaceuticals Corporation Phosphodiesterase 4 inhibitors
EP1579862A1 (en) * 2004-03-25 2005-09-28 Boehringer Ingelheim Vetmedica Gmbh Use of PDE III inhibitors for the reduction of heart size in mammals suffering from heart failure
WO2006050057A2 (en) * 2004-10-28 2006-05-11 Celgene Corporation Methods and compositions using pde4 modulators for treatment and management of central nervous system injury
WO2007030697A2 (en) * 2005-09-07 2007-03-15 Braincells, Inc. Modulation of neurogenesis by hdac inhibition

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
J. CHEN, M. CHOPP ET AL: "Statins Induce Angiogenesis, Neurogenesis and Synaptogenesis after Stroke", ANNALS OF NEUROLOGY, vol. 53, no. 6, June 2003 (2003-06-01), pages 743 - 751, XP002435237 *
KIM J E ET AL: "CHRONIC ADMINISTRATION OF ROLIPRAM, A CYCLIC-AMP PHOSPHODIESTERASE-4 INHIBITOR, UPREGULATES NEUROGENESIS IN THE ADULT MOUSE HIPPOCAMPUS", ABSTRACTS OF THE SOCIETY FOR NEUROSCIENCE, SOCIETY FOR NEUROSCIENCE, WASHINGTON, DC, US, vol. 26, no. 1-2, 2001, pages 2316, XP008078705, ISSN: 0190-5295 *
MALBERG JESSICA E ET AL: "CHRONIC ANTIDEPRESSANT TREATMENT INCREASES NEUROGENESIS IN ADULT RAT HIPPOCAMPUS", JOURNAL OF NEUROSCIENCE, NEW YORK, NY, US, vol. 20, no. 24, 15 December 2000 (2000-12-15), pages 9104 - 9110, XP009077904, ISSN: 0270-6474 *
S. NAKAGAWA ET AL: "Regulation of Neurogenesis in Adult Mouse Hippocampus by cAMP and the cAMP Response Element-Binding Protein", THE JOURNAL OF NEUROSCIENCE, vol. 22, no. 9, May 2002 (2002-05-01), pages 3673 - 3682, XP002435236 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8555875B2 (en) 2008-12-23 2013-10-15 Map Pharmaceuticals, Inc. Inhalation devices and related methods for administration of sedative hypnotic compounds
US9161912B2 (en) 2008-12-23 2015-10-20 Map Pharmaceuticals, Inc. Inhalation devices and related methods for administration of sedative hypnotic compounds

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