ATE541847T1 - Pyrazolopyrimidine als natriumkanalblocker - Google Patents
Pyrazolopyrimidine als natriumkanalblockerInfo
- Publication number
- ATE541847T1 ATE541847T1 AT02792224T AT02792224T ATE541847T1 AT E541847 T1 ATE541847 T1 AT E541847T1 AT 02792224 T AT02792224 T AT 02792224T AT 02792224 T AT02792224 T AT 02792224T AT E541847 T1 ATE541847 T1 AT E541847T1
- Authority
- AT
- Austria
- Prior art keywords
- pyrazolopyrimidines
- compositions
- methods
- sodium channel
- channel blockers
- Prior art date
Links
- 239000003195 sodium channel blocking agent Substances 0.000 title 1
- 238000000034 method Methods 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 208000002193 Pain Diseases 0.000 abstract 2
- 108010052164 Sodium Channels Proteins 0.000 abstract 2
- 102000018674 Sodium Channels Human genes 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000004907 flux Effects 0.000 abstract 2
- 230000005764 inhibitory process Effects 0.000 abstract 2
- APXRHPDHORGIEB-UHFFFAOYSA-N 1H-pyrazolo[4,3-d]pyrimidine Chemical class N1=CN=C2C=NNC2=C1 APXRHPDHORGIEB-UHFFFAOYSA-N 0.000 abstract 1
- 108091006146 Channels Proteins 0.000 abstract 1
- 208000000094 Chronic Pain Diseases 0.000 abstract 1
- 206010065390 Inflammatory pain Diseases 0.000 abstract 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 abstract 1
- 230000000903 blocking effect Effects 0.000 abstract 1
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 230000001419 dependent effect Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 150000002500 ions Chemical class 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 230000002981 neuropathic effect Effects 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
- 208000027232 peripheral nervous system disease Diseases 0.000 abstract 1
- 229910001415 sodium ion Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/495—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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33587401P | 2001-11-01 | 2001-11-01 | |
| PCT/US2002/035171 WO2003037900A2 (en) | 2001-11-01 | 2002-11-01 | Pyrazolopyrimidines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE541847T1 true ATE541847T1 (de) | 2012-02-15 |
Family
ID=23313580
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT02792224T ATE541847T1 (de) | 2001-11-01 | 2002-11-01 | Pyrazolopyrimidine als natriumkanalblocker |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US6833371B2 (de) |
| EP (1) | EP1506196B1 (de) |
| AT (1) | ATE541847T1 (de) |
| CA (1) | CA2465326C (de) |
| WO (1) | WO2003037900A2 (de) |
Families Citing this family (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2379585C (en) * | 1999-09-30 | 2006-06-20 | James W. Darrow | Certain alkylene diamine-substituted pyrazolo[1,5,-a]-1,5-pyrimidines and pyrazolo[1,5-a]-1,3,5-triazines |
| EP1392692B1 (de) * | 2001-03-27 | 2006-11-15 | Neurogen Corporation | (oxopyrazolo¬1,5a|pyrimidin-2-yl) alkylcarbonsäureamide |
| AU2002356525A1 (en) * | 2001-09-24 | 2003-04-07 | Elan Pharmaceuticals, Inc. | Substituted amines for the treatment of neurological disorders |
| US6770484B2 (en) * | 2001-11-29 | 2004-08-03 | Dong C. Liang | Using flame and graphite furnace atomic absorption spectrometry for analysis of sodium channel activity |
| US6908923B2 (en) | 2001-12-21 | 2005-06-21 | Cytokinetics, Inc. | Compositions and methods for treating heart failure |
| CA2498399A1 (en) * | 2002-09-12 | 2004-03-25 | Merck & Co., Inc. | Method of treating diabetes and related conditions |
| US20040085904A1 (en) * | 2002-10-31 | 2004-05-06 | Bordogna Mark A. | Method for flow control of packets aggregated from multiple logical ports over a transport link |
| US20070179161A1 (en) * | 2003-03-31 | 2007-08-02 | Vernalis (Cambridge) Limited. | Pyrazolopyrimidine compounds and their use in medicine |
| WO2004087956A2 (en) * | 2003-04-02 | 2004-10-14 | Ionix Pharmaceuticals Limited | Cell lines for the functional expression of nav1.8 |
| US20060094699A1 (en) * | 2003-04-11 | 2006-05-04 | Kampen Gita Camilla T | Combination therapy using an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and a glucocorticoid receptor agonist to minimize the side effects associated with glucocorticoid receptor agonist therapy |
| EP1782859A3 (de) * | 2003-04-11 | 2009-09-30 | High Point Pharmaceuticals, LLC | Pharmazeutische Verwendung von Pyrazolo [1,5- a] Pyrimidin-Derivaten |
| CN1894222A (zh) * | 2003-08-05 | 2007-01-10 | 沃泰克斯药物股份有限公司 | 作为电压门控离子通道抑制剂的稠合嘧啶化合物 |
| JPWO2005030773A1 (ja) * | 2003-09-26 | 2006-12-07 | 大日本住友製薬株式会社 | 新規ピラゾロピリミジン誘導体 |
| US20050085531A1 (en) * | 2003-10-03 | 2005-04-21 | Hodge Carl N. | Thiophene-based compounds exhibiting ATP-utilizing enzyme inhibitory activity, and compositions, and uses thereof |
| US20080287405A1 (en) * | 2004-05-14 | 2008-11-20 | Thannickal Victor J | Compositions and Methods Relating to Protein Kinase Inhibitors |
| EP1802623A1 (de) * | 2004-10-12 | 2007-07-04 | Novo Nordisk A/S | 11beta-hydroxysteroid-dehydrogenase-typ-1-aktive spiroverbindungen |
| TW200639159A (en) * | 2005-04-22 | 2006-11-16 | Wyeth Corp | Treatment of pain |
| EP1908752A4 (de) * | 2005-06-07 | 2009-09-02 | Dainippon Sumitomo Pharma Co | Neue 2-chinolonderivate |
| EP1926734A1 (de) | 2005-08-22 | 2008-06-04 | Amgen Inc. | Als modulatoren von kinaseenzymen geeignete pyrazolopyridin- und pyrazolopyrimidinverbindungen |
| KR20080069189A (ko) * | 2005-11-01 | 2008-07-25 | 트랜스테크 파르마, 인크. | 치환된 아미드의 약학적 사용 |
| KR20090014347A (ko) | 2006-04-07 | 2009-02-10 | 하이 포인트 파마슈티칼스, 엘엘씨 | 11β-히드록시스테로이드 탈수소효소 타입 1 활성 화합물 |
| EP2038255A2 (de) * | 2006-06-16 | 2009-03-25 | High Point Pharmaceuticals, LLC | Pharmazeutische verwendung substituierter piperidincarbonsäureamide |
| WO2008006702A1 (en) | 2006-07-13 | 2008-01-17 | High Point Pharmaceuticals, Llc. | 11beta-hydroxysteroid dehydrogenase type 1 active compounds |
| ES2359447T3 (es) * | 2006-08-04 | 2011-05-23 | MERZ PHARMA GMBH & CO. KGAA | Pirazolopirimidinas sustituidas, un proceso para su preparación y su uso como medicina. |
| MX2009001036A (es) * | 2006-08-04 | 2009-04-23 | Merz Pharma Gmbh & Co Kgaa | Pirazolopirimidinas, proceso para su preparacion y su uso como medicina. |
| WO2008056176A1 (en) * | 2006-11-10 | 2008-05-15 | Scottish Biomedical Limited | Pyrazolopyrimidines as phosphodiesterase inhibitors |
| JP2010043004A (ja) * | 2006-12-06 | 2010-02-25 | Dainippon Sumitomo Pharma Co Ltd | 新規2環性複素環化合物 |
| EP2150526B1 (de) | 2007-02-23 | 2017-09-20 | vTv Therapeutics LLC | N-adamantylbenzamide als inhibitoren von 11-beta-hydroxysteroid dehydrogenase |
| EP2129652A2 (de) | 2007-02-23 | 2009-12-09 | High Point Pharmaceuticals, LLC | N-adamantylbenzamide als inhibitoren von 11-beta-hydroxysteroiddehydrogenase |
| WO2008110196A1 (en) | 2007-03-09 | 2008-09-18 | High Point Pharmaceuticals, Llc | Indole- and benzimidazole amides as hydroxysteroid dehydrogenase inhibitors |
| ES2393230T3 (es) | 2007-04-24 | 2012-12-19 | High Point Pharmaceuticals, Llc | Uso farmacéutico de amidas sustituidas |
| CN101835377B (zh) | 2007-08-27 | 2014-12-10 | 巴斯夫欧洲公司 | 用于防治无脊椎动物害虫的吡唑化合物 |
| US9050350B2 (en) | 2007-10-18 | 2015-06-09 | U.S. Department Of Veterans Affairs | Method for modulating or controlling connexin 43(Cx43) level of a cell and reducing arrhythmic risk |
| US9220720B2 (en) | 2007-10-18 | 2015-12-29 | U.S. Department Of Veterans Affairs | Method for ameliorating or preventing arrhythmic risk associated with cardiomyopathy |
| US9114151B2 (en) * | 2007-10-18 | 2015-08-25 | The United States Of America Dept. Of Veterans Affairs | Method for modulating or controlling sodium channel current by reactive oxygen species (ROS) originating from mitochondria |
| US8003324B2 (en) * | 2007-10-18 | 2011-08-23 | U.S. Department Of Veterans Affairs | Modulation of sodium channels by nicotinamide adenine dinucleotide |
| US9211301B2 (en) | 2007-10-18 | 2015-12-15 | U.S. Department Of Veterans Affairs | Method for ameliorating or preventing arrhythmic risk associated with cardiomyopathy by improving conduction velocity |
| EP2085398A1 (de) | 2008-02-01 | 2009-08-05 | Merz Pharma GmbH & Co. KGaA | Pyrazolopyrimidine, Verfahren zu ihrer Herstellung und Verwendung als Arzneimittel |
| EP2090576A1 (de) * | 2008-02-01 | 2009-08-19 | Merz Pharma GmbH & Co.KGaA | 6-halo-Pyrazolo[1,5-a]pyridin-Verbindungen, Verfahren zu ihrer Herstellung und Verwendung als Modulatoren des Metabotropen Glutamatrezeptoren (mGluR) |
| KR20100124262A (ko) | 2008-02-13 | 2010-11-26 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 비시클로아민 유도체 |
| KR101364869B1 (ko) | 2008-09-24 | 2014-02-21 | 바스프 에스이 | 무척추 해충을 방제하기 위한 피라졸 화합물 |
| EP2346335B1 (de) * | 2008-09-24 | 2018-11-14 | Basf Se | Pyrazolverbindungen für die bekämpfung von wirbellosen schädlingen |
| US8927549B2 (en) * | 2008-11-21 | 2015-01-06 | High Point Pharmaceuticals, Llc | Adamantyl benzamide derivatives |
| EP2451804B1 (de) | 2009-07-06 | 2014-04-30 | Basf Se | Pyridazinverbindungen zur bekämpfung von wirbellosen schädlingen |
| ES2461618T3 (es) | 2009-07-06 | 2014-05-20 | Basf Se | Compuestos de piridacina para el control de plagas de invertebrados |
| JP2013500246A (ja) | 2009-07-24 | 2013-01-07 | ビーエーエスエフ ソシエタス・ヨーロピア | 無脊椎動物系害虫防除用ピリジン誘導体化合物 |
| WO2012015715A1 (en) | 2010-07-27 | 2012-02-02 | High Point Pharmaceuticals, Llc | Substituted thiazol-2-ylamine derivatives, pharmaceutical compositions, and methods of use as 11-beta hsd1 modulators |
| WO2012139876A1 (en) | 2011-04-14 | 2012-10-18 | Merz Pharma Gmbh & Co. Kgaa | Enteric formulations of metabotropic glutamate receptor modulators |
| US9309250B2 (en) | 2011-06-22 | 2016-04-12 | Vertex Pharmaceuticals Incorporated | Substituted pyrrolo[2,3-b]pyrazines as ATR kinase inhibitors |
| WO2013087808A1 (en) | 2011-12-15 | 2013-06-20 | Merz Pharma Gmbh & Co. Kgaa | Pharmaceutical composition comprising a pyrazolopyrimidme and cyclodextrin |
| WO2013087815A1 (en) | 2011-12-15 | 2013-06-20 | Merz Pharma Gmbh & Co. Kgaa | Liquid pharmaceutical composition containing a pyrazolopyrimidine derivative and pharmaceutical uses thereof |
| RU2015106013A (ru) * | 2012-08-10 | 2016-10-10 | Ф. Хоффманн-Ля Рош Аг | Соединения пиразолкарбоксамида, композиции и способы применения |
| SI2941432T1 (en) | 2012-12-07 | 2018-07-31 | Vertex Pharmaceuticals Incorporated | 2-AMINO-6-FLUORO-N- (5-FLUORO-4- (4- (4- (OXETHAN-3-YL) PIPERAZIN-1-CARBONYL) PIPERIDIN-1-YLIPRIDIN-3-YL) 1,5 ALFA) PYRIMIDINE-3-CARBOXAMIDE AS ATR KINAZE INHIBITOR |
| BR112015019276A2 (pt) | 2013-02-19 | 2017-07-18 | Pfizer | compostos de azabenzimidazol como inibidores de isoenzimas de pde4 para o tratamento de distúrbios do snc e outros distúrbios |
| US8957078B2 (en) | 2013-03-15 | 2015-02-17 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| WO2014143240A1 (en) | 2013-03-15 | 2014-09-18 | Vertex Pharmaceuticals Incorporated | Fused pyrazolopyrimidine derivatives useful as inhibitors of atr kinase |
| EP2970288A1 (de) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Incorporated | Als atr-kinaseinhibitoren nützliche verbindungen |
| HK1223096A1 (zh) * | 2013-09-25 | 2017-07-21 | Vertex Pharmaceuticals Incorporated | 用作par-2信號通路抑制劑的咪唑並噠嗪 |
| PT3077397T (pt) | 2013-12-06 | 2020-01-22 | Vertex Pharma | Composto de 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]pirazolo[1,5-a]pirimidin-3-carboxamida útil como inibidor da atr quinase, a sua preparação, diferentes formas sólidas e derivados radiomarcados do mesmo |
| MX373102B (es) | 2014-06-05 | 2020-04-17 | Vertex Pharma | Derivados radiomarcados de un compuesto de 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]-pirazolo[1,5-a]pirimidin-3-carboxamida útil como inhibidor de ataxia telangiectasia mutada y rad3 relacionado (atr) cinasa, preparación de tal compuesto y diferentes formas sólidas del mismo. |
| SG11201610500WA (en) | 2014-06-17 | 2017-01-27 | Vertex Pharma | Method for treating cancer using a combination of chk1 and atr inhibitors |
| WO2016012896A1 (en) | 2014-07-24 | 2016-01-28 | Pfizer Inc. | Pyrazolopyrimidine compounds |
| MD20170011A2 (ro) | 2014-08-06 | 2017-08-31 | Pfizer Inc. | Compuşi imidazopiridazinici |
| AU2016331955B2 (en) | 2015-09-30 | 2022-07-21 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of DNA damaging agents and ATR inhibitors |
| TWI732031B (zh) * | 2016-08-31 | 2021-07-01 | 日商衛材R&D企管股份有限公司 | 吡唑并[1, 5-a]嘧啶化合物 |
| WO2019163956A1 (ja) | 2018-02-26 | 2019-08-29 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | ピラゾロ[1,5-a]ピリミジン化合物の塩およびその結晶 |
| US20240018151A1 (en) * | 2020-10-19 | 2024-01-18 | Tme Therapeutics Llc | Novel inhibitors of pikfyve and methods using same |
| AU2021363703A1 (en) * | 2020-10-23 | 2023-06-22 | S2Cbio Inc. | Cftr modulator compounds, compositions, and uses thereof |
| JP2024508761A (ja) * | 2020-12-18 | 2024-02-28 | ザ スクリプス リサーチ インスティテュート | 神経変性、変性及び代謝性障害の処置のための化合物並びにその使用 |
| CA3249844A1 (en) * | 2022-01-27 | 2023-08-03 | Janssen Pharmaceutica Nv | PYRAZOLOPYRIMIDINES USED AS SPERM OXIDASE MODULATORS |
| CN119137102A (zh) * | 2022-04-08 | 2024-12-13 | 拜奥列司治疗有限公司 | Cdk9抑制剂 |
| US20250114357A1 (en) * | 2023-10-10 | 2025-04-10 | Biolexis Therapeutics, Inc. | Bifunctional protac and molecular glue compounds and methods of use thereof |
| CN119033788B (zh) * | 2024-08-27 | 2025-10-31 | 南京中医药大学 | 分枝杆菌硫醇二硫还原酶抑制剂在制备抗分枝杆菌药物中的应用 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4178449A (en) * | 1978-04-17 | 1979-12-11 | American Cyanamid Company | Pyrazolo[1,5-a]pyrimidines and imidazo-[1,5-a]pyrimidines |
| US5571813A (en) * | 1993-06-10 | 1996-11-05 | Beiersdorf-Lilly Gmbh | Fused pyrimidine compounds and their use as pharmaceuticals |
| WO1995035298A1 (en) * | 1994-06-21 | 1995-12-28 | Otsuka Pharmaceutical Factory, Inc. | PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVE |
| KR100271998B1 (ko) * | 1995-04-10 | 2001-02-01 | 오쓰카 요시미쓰 | 피라졸로(1,5-a)피리미딘유도체 |
| US5843951A (en) * | 1995-09-28 | 1998-12-01 | Otsuka Pharmaceutical Factory Inc. | Analgesic composition of pyrazolo(1,5-A) pyrimidines |
| JP4000433B2 (ja) * | 1998-01-29 | 2007-10-31 | 株式会社大塚製薬工場 | ピラゾロ〔1,5−a〕ピリミジン誘導体 |
| MY125533A (en) * | 1999-12-06 | 2006-08-30 | Bristol Myers Squibb Co | Heterocyclic dihydropyrimidine compounds |
| GB0002666D0 (en) * | 2000-02-04 | 2000-03-29 | Univ London | Blockade of voltage dependent sodium channels |
| AU4589701A (en) * | 2000-03-24 | 2001-10-08 | Cocensys Inc | Aryl substituted pyrazoles, triazoles and tetrazoles, and the use thereof |
| DE10112197A1 (de) * | 2001-03-14 | 2002-09-19 | Gruenenthal Gmbh | Substituierte Pyrazolo- und Thiazolopyrimidine |
| DE10153344A1 (de) * | 2001-10-29 | 2003-05-15 | Gruenenthal Gmbh | Verwendung von substituierten Pyrazolopyrimidinen als Liganden von Nucleosid-Transport-Proteinen und/oder von Purinorezeptoren |
| WO2004001058A2 (en) * | 2001-05-04 | 2003-12-31 | Paratek Pharmaceuticals, Inc. | Transcription factor modulating compounds and methods of use thereof |
-
2002
- 2002-11-01 CA CA2465326A patent/CA2465326C/en not_active Expired - Fee Related
- 2002-11-01 WO PCT/US2002/035171 patent/WO2003037900A2/en not_active Ceased
- 2002-11-01 US US10/286,687 patent/US6833371B2/en not_active Expired - Fee Related
- 2002-11-01 EP EP02792224A patent/EP1506196B1/de not_active Expired - Lifetime
- 2002-11-01 AT AT02792224T patent/ATE541847T1/de active
-
2004
- 2004-11-12 US US10/987,089 patent/US7098335B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US7098335B2 (en) | 2006-08-29 |
| EP1506196B1 (de) | 2012-01-18 |
| US20030176450A1 (en) | 2003-09-18 |
| WO2003037900A2 (en) | 2003-05-08 |
| CA2465326A1 (en) | 2003-05-08 |
| US6833371B2 (en) | 2004-12-21 |
| EP1506196A2 (de) | 2005-02-16 |
| EP1506196A4 (de) | 2008-01-02 |
| US20050215569A1 (en) | 2005-09-29 |
| WO2003037900A3 (en) | 2004-11-18 |
| CA2465326C (en) | 2011-03-29 |
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