HK1071127A1 - A2b adenosine receptor antagonists a2b - Google Patents
A2b adenosine receptor antagonists a2bInfo
- Publication number
- HK1071127A1 HK1071127A1 HK05101136.8A HK05101136A HK1071127A1 HK 1071127 A1 HK1071127 A1 HK 1071127A1 HK 05101136 A HK05101136 A HK 05101136A HK 1071127 A1 HK1071127 A1 HK 1071127A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- receptor antagonists
- adenosine receptor
- sub
- formula
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
- C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/04—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
- C07D473/06—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
- C07D473/08—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US34822201P | 2001-11-09 | 2001-11-09 | |
US40140802P | 2002-08-05 | 2002-08-05 | |
PCT/US2002/035880 WO2003042214A2 (fr) | 2001-11-09 | 2002-11-08 | Antagonistes de recepteur d'adenosine a¿2b? |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1071127A1 true HK1071127A1 (en) | 2005-07-08 |
Family
ID=26995608
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK05101136.8A HK1071127A1 (en) | 2001-11-09 | 2005-02-12 | A2b adenosine receptor antagonists a2b |
Country Status (20)
Country | Link |
---|---|
US (2) | US6825349B2 (fr) |
EP (1) | EP1444233B1 (fr) |
JP (1) | JP4350517B2 (fr) |
KR (1) | KR100937620B1 (fr) |
CN (1) | CN100467469C (fr) |
AT (1) | ATE520694T1 (fr) |
AU (1) | AU2002359365B2 (fr) |
CA (1) | CA2466477C (fr) |
CY (1) | CY1112459T1 (fr) |
DK (1) | DK1444233T3 (fr) |
HK (1) | HK1071127A1 (fr) |
HU (1) | HU229504B1 (fr) |
IL (2) | IL161867A0 (fr) |
MX (1) | MXPA04004388A (fr) |
NO (1) | NO329692B1 (fr) |
NZ (1) | NZ532816A (fr) |
PL (1) | PL370207A1 (fr) |
PT (1) | PT1444233E (fr) |
RU (1) | RU2318824C2 (fr) |
WO (1) | WO2003042214A2 (fr) |
Families Citing this family (71)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
USRE47351E1 (en) | 1999-06-22 | 2019-04-16 | Gilead Sciences, Inc. | 2-(N-pyrazolo)adenosines with application as adenosine A2A receptor agonists |
US6403567B1 (en) * | 1999-06-22 | 2002-06-11 | Cv Therapeutics, Inc. | N-pyrazole A2A adenosine receptor agonists |
AU2001238665A1 (en) | 2000-02-23 | 2001-09-03 | Cv Therapeutics, Inc. | Method of identifying partial agonists of the a2a receptor |
HUP0301622A3 (en) * | 2000-07-04 | 2006-05-29 | Novo Nordisk As | Purine derivatives inhibiting the enzyme dipeptidyl petidase iv (dpp-iv) and pharmaceutical compositions containing them |
US7317017B2 (en) * | 2002-11-08 | 2008-01-08 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
US20080194593A1 (en) * | 2001-11-09 | 2008-08-14 | Rao Kalla | A2b adenosine receptor antagonists |
US6977300B2 (en) * | 2001-11-09 | 2005-12-20 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
US7304070B2 (en) * | 2001-11-09 | 2007-12-04 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
US7125993B2 (en) * | 2001-11-09 | 2006-10-24 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
US20080318983A1 (en) * | 2001-11-09 | 2008-12-25 | Rao Kalla | A2b adenosine receptor antagonists |
US7205403B2 (en) * | 2002-02-01 | 2007-04-17 | King Pharmaceuticals Research And Development, Inc. | 8-Heteroaryl xanthine adenosine A2B receptor antagonists |
AU2003254650B2 (en) * | 2002-07-24 | 2010-09-09 | Qlt, Inc. | Pyrazolylbenzothiazole derivatives and their use as therapeutic agents |
US20050020915A1 (en) * | 2002-07-29 | 2005-01-27 | Cv Therapeutics, Inc. | Myocardial perfusion imaging methods and compositions |
US8470801B2 (en) | 2002-07-29 | 2013-06-25 | Gilead Sciences, Inc. | Myocardial perfusion imaging methods and compositions |
EP1524984A1 (fr) * | 2002-07-29 | 2005-04-27 | Cv Therapeutics, Inc. | Imagerie de perfusion myocardique au moyen d'agonistes de recepteur a2a |
DE60322748D1 (de) * | 2003-05-06 | 2008-09-18 | Cv Therapeutics Inc | Xanthinderivate als a2b-adenosinrezeptorantagonisten |
AU2011224104B2 (en) * | 2003-05-06 | 2012-06-28 | Gilead Sciences, Inc. | A2B adenosine receptor antagonists |
ES2440467T3 (es) * | 2003-08-25 | 2014-01-29 | Dogwood Pharmaceuticals, Inc. | 8-heteroaril xantinas substituidas |
AU2004285013A1 (en) * | 2003-10-31 | 2005-05-12 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
AU2011202523B2 (en) * | 2003-11-21 | 2013-05-30 | Gilead Sciences, Inc. | A2B adenosine receptor antagonists |
GB0411056D0 (en) | 2004-05-18 | 2004-06-23 | Novartis Ag | Organic compounds |
RU2385322C2 (ru) * | 2004-09-01 | 2010-03-27 | Си Ви Терапьютикс, Инк. | Способ заживления ран с применением антагонистов аденозинового рецептора a2b |
EP1799221A1 (fr) * | 2004-10-15 | 2007-06-27 | Cv Therapeutics, Inc. | Procede de prevention et de traitement du remodelage des voies respiratoires et de l'inflammation pulmonaire par le biais d'antagonistes du recepteur d'adenosine a2b |
KR20070083714A (ko) | 2004-10-20 | 2007-08-24 | 씨브이 쎄러퓨틱스, 인코포레이티드 | A2a 아데노신 수용체 작용제의 용도 |
US7598379B2 (en) | 2005-02-25 | 2009-10-06 | Pgx Health, Llc | Methods for the synthesis of unsymmetrical cycloalkyl substituted xanthines |
WO2006091897A2 (fr) * | 2005-02-25 | 2006-08-31 | Adenosine Therapeutics, Llc | Derives de xanthines substituees en 8 |
US7618962B2 (en) | 2005-02-25 | 2009-11-17 | Pgx Health, Llc | Pyrazolyl substituted xanthines |
CN101198608B (zh) * | 2005-06-16 | 2011-04-27 | 吉利德帕洛阿尔托股份有限公司 | A2b腺苷受体拮抗剂的前药 |
ES2270715B1 (es) | 2005-07-29 | 2008-04-01 | Laboratorios Almirall S.A. | Nuevos derivados de pirazina. |
ES2274712B1 (es) | 2005-10-06 | 2008-03-01 | Laboratorios Almirall S.A. | Nuevos derivados imidazopiridina. |
GB0601951D0 (en) | 2006-01-31 | 2006-03-15 | Novartis Ag | Organic compounds |
PL1989214T3 (pl) | 2006-02-03 | 2017-07-31 | Gilead Sciences, Inc. | Proces otrzymywania agonisty receptora adenozynowego a2a i jego polimorfów |
MX2008011828A (es) * | 2006-03-17 | 2008-09-29 | Cv Therapeutics Inc | Metodo para la prevencion y el tratamiento de enfermedad hepatica utilizando antagonistas del receptor de adenosina a2b. |
US7884100B2 (en) * | 2006-06-16 | 2011-02-08 | Pgxhealth, Llc | Substituted 8-[6-amino-3-pyridyl]xanthines |
US7767685B2 (en) * | 2006-06-29 | 2010-08-03 | King Pharmaceuticals Research And Development, Inc. | Adenosine A2B receptor antagonists |
WO2008028140A1 (fr) * | 2006-09-01 | 2008-03-06 | Cv Therapeutics, Inc. | Méthodes et compositions permettant d'augmenter la tolérabilité de patients pendant des méthodes d'imagerie myocardique |
US7470697B2 (en) * | 2006-09-01 | 2008-12-30 | Adenosine Therapeutics, Llc | Pyrrolo[3,2-D] pyrimidines that are selective antagonists of A2B adenosine receptors |
US20090081120A1 (en) * | 2006-09-01 | 2009-03-26 | Cv Therapeutics, Inc. | Methods and Compositions for Increasing Patient Tolerability During Myocardial Imaging Methods |
JP2011502101A (ja) * | 2006-09-29 | 2011-01-20 | ギリアード・パロ・アルト・インコーポレイテッド | 肺疾患の病歴を有する患者における心筋画像化法 |
CN101522682A (zh) | 2006-10-30 | 2009-09-02 | 诺瓦提斯公司 | 作为抗炎剂的杂环化合物 |
JP2010515081A (ja) * | 2007-01-03 | 2010-05-06 | ギリアード・パロ・アルト・インコーポレイテッド | 心筋灌流画像化 |
WO2009076352A1 (fr) * | 2007-12-11 | 2009-06-18 | Schering Corporation | Modulateurs de gamma sécrétase |
PL2231642T3 (pl) | 2008-01-11 | 2014-04-30 | Novartis Ag | Pirymidyny jako inhibitory kinazy |
WO2009088518A1 (fr) * | 2008-01-11 | 2009-07-16 | Cv Therapeutics, Inc. | Antagonistes du récepteur d'adénosine a2b pour le traitement du cancer |
JP5460690B2 (ja) * | 2008-03-26 | 2014-04-02 | アドヴィナス・セラピューティックス・リミテッド | アデノシンレセプターアンタゴニストとしてのヘテロ環化合物 |
WO2009157938A1 (fr) * | 2008-06-26 | 2009-12-30 | Cv Therapeutics, Inc. | Antagonistes de récepteur d’adénosine a2b pour traiter le cancer |
US20110118276A1 (en) * | 2008-07-16 | 2011-05-19 | Edward Leung | Methods of treating atherosclerosis |
JP2012504147A (ja) * | 2008-09-29 | 2012-02-16 | ギリアード サイエンシーズ, インコーポレイテッド | 多検出器型コンピュータ断層撮影法において使用するための心拍数コントロール薬およびA−2−α受容体作動薬の組み合わせ |
WO2010103547A2 (fr) | 2009-03-13 | 2010-09-16 | Advinus Therapeutics Private Limited | Composés de pyrimidine fusionnée substituée |
WO2011005871A1 (fr) | 2009-07-07 | 2011-01-13 | Pgxhealth, Llc | 8-[6-carbonylamino-3-pyridyle] xanthines substituées en tant quantagonistes de ladénosine a2b |
WO2011055391A1 (fr) | 2009-11-09 | 2011-05-12 | Advinus Therapeutics Private Limited | Composés pyrimidine fusionnés substitués, leur préparation et leurs utilisations |
CA2802891A1 (fr) * | 2010-06-30 | 2012-01-05 | Gilead Sciences, Inc. | Utilisation d'antagonistes de recepteur d'adenosine a2b pour traiter l'hypertension pulmonaire |
US8637516B2 (en) | 2010-09-09 | 2014-01-28 | Irm Llc | Compounds and compositions as TRK inhibitors |
WO2012034095A1 (fr) | 2010-09-09 | 2012-03-15 | Irm Llc | Composés et compositions comme inhibiteurs de trk |
AU2011303420B2 (en) * | 2010-09-13 | 2014-03-20 | Impetis Biosciences Ltd. | Purine compounds as prodrugs of A2B adenosine receptor antagonists, their process and medicinal applications |
EP2465859A1 (fr) * | 2010-12-08 | 2012-06-20 | Life & Brain GmbH | Dérivés de 8-triazolylxanthine, leurs procédés de production et leur utilisation en tant qu'antagonistes du récepteur de l'adénosine |
CA2828219A1 (fr) | 2011-02-25 | 2012-08-30 | Irm Llc | Composes et compositions en tant qu'inhibiteurs de trk |
AR085942A1 (es) | 2011-04-07 | 2013-11-06 | Gilead Sciences Inc | Uso de receptor de aadenosina para tratar la insuficiencia cardiaca y la arritmia en pacientes posinfarto de miocardio |
CN104010641B (zh) * | 2011-10-27 | 2017-04-12 | 普罗塔医药公司 | 用于治疗淀粉样蛋白病和共核蛋白病的含咖啡因的化合物和组合物 |
CN102532137B (zh) * | 2011-12-05 | 2014-12-10 | 辽宁医学院 | 8-吡唑取代黄嘌呤类a2b腺苷受体拮抗剂及其合成方法和应用 |
JP6132853B2 (ja) * | 2011-12-27 | 2017-05-24 | アラーガン、インコーポレイテッドAllergan,Incorporated | 全身性抗炎症反応を提供する、複数のプロスタグランジン受容体で作用する化合物 |
JP6360149B2 (ja) | 2013-03-15 | 2018-07-18 | ハイドラ バイオサイエンシズ インコーポレイテッドHydra Biosciences,Inc. | 置換キサンチンおよびその使用方法 |
WO2014153424A1 (fr) * | 2013-03-19 | 2014-09-25 | La Jolla Institute For Allergy And Immunology | Réduction de diabète chez des patients recevant des inhibiteurs de l'hmg-coa réductase (statines) |
CN104744469A (zh) * | 2014-10-31 | 2015-07-01 | 合肥平光制药有限公司 | 一种茶碱的制备方法 |
WO2017060488A1 (fr) * | 2015-10-09 | 2017-04-13 | Almirall, S.A. | Nouveaux antagonistes de trpa1 |
EP3414319A4 (fr) | 2016-02-10 | 2019-08-28 | Wake Forest University Health Sciences | Système modèle de fibrose hépatique et son procédé de fabrication et d'utilisation |
CN112218867B (zh) | 2018-03-05 | 2023-11-21 | 泰昂治疗公司 | 腺苷受体拮抗剂及其用途 |
US10710994B2 (en) | 2018-03-19 | 2020-07-14 | Genentech, Inc. | Oxadiazole transient receptor potential channel inhibitors |
KR20210061202A (ko) | 2019-11-19 | 2021-05-27 | 일동제약(주) | 벤조나이트릴이 치환된 축합 피리미딘 유도체 및 그의 의약 용도 |
KR20210076693A (ko) | 2019-12-16 | 2021-06-24 | 일동제약(주) | 질소를 포함하는 헤테로고리로 치환된 축합 피리미딘 유도체 및 그의 의약 용도 |
WO2024015372A1 (fr) | 2022-07-14 | 2024-01-18 | Teon Therapeutics, Inc. | Antagonistes des récepteurs de l'adénosine et leurs utilisations |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3845770A (en) | 1972-06-05 | 1974-11-05 | Alza Corp | Osmatic dispensing device for releasing beneficial agent |
US4326525A (en) | 1980-10-14 | 1982-04-27 | Alza Corporation | Osmotic device that improves delivery properties of agent in situ |
US4452788A (en) | 1982-04-21 | 1984-06-05 | Warner-Lambert Company | Substituted 8-phenylxanthines |
US4593095A (en) | 1983-02-18 | 1986-06-03 | The Johns Hopkins University | Xanthine derivatives |
US4558051A (en) | 1983-10-11 | 1985-12-10 | Richardson-Vicks, Inc. | Analgesic and anti-inflammatory compositions comprising xanthines and methods of using same |
US5364620A (en) | 1983-12-22 | 1994-11-15 | Elan Corporation, Plc | Controlled absorption diltiazem formulation for once daily administration |
GB8510758D0 (en) * | 1985-04-27 | 1985-06-05 | Wellcome Found | Compounds |
US5023252A (en) | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
US4992445A (en) | 1987-06-12 | 1991-02-12 | American Cyanamid Co. | Transdermal delivery of pharmaceuticals |
US5001139A (en) | 1987-06-12 | 1991-03-19 | American Cyanamid Company | Enchancers for the transdermal flux of nivadipine |
US4902514A (en) | 1988-07-21 | 1990-02-20 | Alza Corporation | Dosage form for administering nilvadipine for treating cardiovascular symptoms |
DE8817122U1 (fr) | 1988-12-22 | 1993-02-04 | Boehringer Ingelheim Kg, 6507 Ingelheim, De | |
IT1229195B (it) | 1989-03-10 | 1991-07-25 | Poli Ind Chimica Spa | Derivati xantinici ad attivita' broncodilatatrice e loro applicazioni terapeutiche. |
DE4019892A1 (de) | 1990-06-22 | 1992-01-02 | Boehringer Ingelheim Kg | Neue xanthinderivate |
WO1995011681A1 (fr) * | 1993-10-29 | 1995-05-04 | Merck & Co., Inc. | Antagonistes du recepteur de l'adenosine humaine |
GB9415529D0 (en) * | 1994-08-01 | 1994-09-21 | Wellcome Found | Phenyl xanthine derivatives |
DE19535504A1 (de) | 1995-09-25 | 1997-03-27 | Bayer Ag | Substituierte Xanthine |
US6291501B1 (en) | 1998-02-20 | 2001-09-18 | Harbor Branch Oceanographic Institution, Inc. | Compounds and methods of use for treatment of neurogenic inflammation |
US6117878A (en) | 1998-02-24 | 2000-09-12 | University Of Virginia | 8-phenyl- or 8-cycloalkyl xanthine antagonists of A2B human adenosine receptors |
DE69812070T2 (de) | 1998-04-24 | 2003-12-11 | K U Leuven Res & Dev Leuven | Immununterdrückende Effekte von 8 substituierten Xanthinderivaten |
DE29902571U1 (de) | 1998-05-19 | 2000-03-23 | Papst Motoren Gmbh & Co Kg | Elektronisch kommutierter Motor |
US6060481A (en) | 1998-05-28 | 2000-05-09 | The Penn State Research Foundation | Method for improving insulin sensitivity using an adenosine receptor antagonist |
CA2333947C (fr) * | 1998-06-01 | 2010-09-21 | Fujisawa Pharmaceutical Co., Ltd. | Composes de pyrazolopyridine utilises en tant qu'antagonistes de l'adenosine a1 contre l'infertilite masculine |
GB9817623D0 (en) | 1998-08-13 | 1998-10-07 | Glaxo Group Ltd | Pharmaceutical compounds |
US6545002B1 (en) | 1999-06-01 | 2003-04-08 | University Of Virginia Patent Foundation | Substituted 8-phenylxanthines useful as antagonists of A2B adenosine receptors |
US6437154B1 (en) | 2001-09-28 | 2002-08-20 | Council Of Scientific And Industrial Research | Process for the preparation of 10-deacetylbaccatin III |
US7317017B2 (en) * | 2002-11-08 | 2008-01-08 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
US6977300B2 (en) * | 2001-11-09 | 2005-12-20 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
US7247639B2 (en) * | 2003-06-06 | 2007-07-24 | Endacea, Inc. | A1 adenosine receptor antagonists |
-
2002
- 2002-11-08 AU AU2002359365A patent/AU2002359365B2/en not_active Ceased
- 2002-11-08 CN CNB02822258XA patent/CN100467469C/zh not_active Expired - Fee Related
- 2002-11-08 MX MXPA04004388A patent/MXPA04004388A/es active IP Right Grant
- 2002-11-08 PT PT02793897T patent/PT1444233E/pt unknown
- 2002-11-08 HU HU0401925A patent/HU229504B1/hu not_active IP Right Cessation
- 2002-11-08 NZ NZ532816A patent/NZ532816A/en not_active IP Right Cessation
- 2002-11-08 AT AT02793897T patent/ATE520694T1/de active
- 2002-11-08 PL PL02370207A patent/PL370207A1/xx not_active Application Discontinuation
- 2002-11-08 CA CA2466477A patent/CA2466477C/fr not_active Expired - Fee Related
- 2002-11-08 KR KR1020047006955A patent/KR100937620B1/ko active IP Right Grant
- 2002-11-08 IL IL16186702A patent/IL161867A0/xx unknown
- 2002-11-08 RU RU2004114210/04A patent/RU2318824C2/ru not_active IP Right Cessation
- 2002-11-08 EP EP02793897A patent/EP1444233B1/fr not_active Expired - Lifetime
- 2002-11-08 JP JP2003544050A patent/JP4350517B2/ja not_active Expired - Fee Related
- 2002-11-08 DK DK02793897.6T patent/DK1444233T3/da active
- 2002-11-08 WO PCT/US2002/035880 patent/WO2003042214A2/fr active IP Right Grant
- 2002-11-08 US US10/290,921 patent/US6825349B2/en not_active Expired - Lifetime
-
2004
- 2004-05-06 IL IL161867A patent/IL161867A/en not_active IP Right Cessation
- 2004-06-08 NO NO20042378A patent/NO329692B1/no not_active IP Right Cessation
- 2004-09-23 US US10/947,708 patent/US7105665B2/en not_active Expired - Lifetime
-
2005
- 2005-02-12 HK HK05101136.8A patent/HK1071127A1/xx not_active IP Right Cessation
-
2011
- 2011-10-31 CY CY20111101035T patent/CY1112459T1/el unknown
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Date | Code | Title | Description |
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PC | Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee) |
Effective date: 20191108 |