WO2007047978A3 - Modulation of neurogenesis by pde inhibition - Google Patents
Modulation of neurogenesis by pde inhibition Download PDFInfo
- 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
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- neurogenesis
- modulation
- pde inhibition
- pde
- stimulate
- Prior art date
Links
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic 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
- A61K31/401—Proline; Derivatives thereof, e.g. captopril
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic 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
- A61K31/4015—Heterocyclic 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic 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
- A61K31/403—Heterocyclic 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/4164—1,3-Diazoles
- A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61P9/10—Drugs 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
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 |
Family
ID=37963343
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/041131 WO2007047978A2 (en) | 2005-10-21 | 2006-10-20 | Modulation of neurogenesis by pde inhibition |
Country Status (6)
Country | Link |
---|---|
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)
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)
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 |
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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)
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)
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 & 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 & 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 & 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 |
-
2006
- 2006-10-20 CA CA002625153A patent/CA2625153A1/en not_active Abandoned
- 2006-10-20 EP EP06826395A patent/EP1940389A2/en not_active Withdrawn
- 2006-10-20 AU AU2006304787A patent/AU2006304787A1/en not_active Abandoned
- 2006-10-20 WO PCT/US2006/041131 patent/WO2007047978A2/en active Application Filing
- 2006-10-20 JP JP2008536840A patent/JP2009512711A/en active Pending
- 2006-10-20 US US11/551,667 patent/US7985756B2/en not_active Expired - Fee Related
- 2006-10-20 EP EP10013573A patent/EP2377530A3/en not_active Withdrawn
Patent Citations (4)
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)
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)
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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WO2007047978A2 (en) | 2007-04-26 |
US20070208029A1 (en) | 2007-09-06 |
EP2377530A3 (en) | 2012-06-20 |
EP1940389A2 (en) | 2008-07-09 |
JP2009512711A (en) | 2009-03-26 |
AU2006304787A1 (en) | 2007-04-26 |
EP2377530A2 (en) | 2011-10-19 |
US7985756B2 (en) | 2011-07-26 |
CA2625153A1 (en) | 2007-04-26 |
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