JP2005511699A5 - - Google Patents

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Publication number
JP2005511699A5
JP2005511699A5 JP2003549355A JP2003549355A JP2005511699A5 JP 2005511699 A5 JP2005511699 A5 JP 2005511699A5 JP 2003549355 A JP2003549355 A JP 2003549355A JP 2003549355 A JP2003549355 A JP 2003549355A JP 2005511699 A5 JP2005511699 A5 JP 2005511699A5
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JP
Japan
Prior art keywords
group
substituents
aryl
halogen
alkyl
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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JP2003549355A
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English (en)
Japanese (ja)
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JP2005511699A (ja
JP4284182B2 (ja
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Application filed filed Critical
Priority claimed from PCT/US2002/037710 external-priority patent/WO2003048165A1/en
Publication of JP2005511699A publication Critical patent/JP2005511699A/ja
Publication of JP2005511699A5 publication Critical patent/JP2005511699A5/ja
Application granted granted Critical
Publication of JP4284182B2 publication Critical patent/JP4284182B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2003549355A 2001-11-30 2002-11-26 アデノシンA2aレセプターアンタゴニスト Expired - Fee Related JP4284182B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US33434201P 2001-11-30 2001-11-30
PCT/US2002/037710 WO2003048165A1 (en) 2001-11-30 2002-11-26 ADENOSINE A2a RECEPTOR ANTAGONISTS

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2008147306A Division JP2008260776A (ja) 2001-11-30 2008-06-04 アデノシンA2aレセプターアンタゴニスト

Publications (3)

Publication Number Publication Date
JP2005511699A JP2005511699A (ja) 2005-04-28
JP2005511699A5 true JP2005511699A5 (US07794700-20100914-C00152.png) 2005-12-22
JP4284182B2 JP4284182B2 (ja) 2009-06-24

Family

ID=23306779

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2003549355A Expired - Fee Related JP4284182B2 (ja) 2001-11-30 2002-11-26 アデノシンA2aレセプターアンタゴニスト
JP2008147306A Pending JP2008260776A (ja) 2001-11-30 2008-06-04 アデノシンA2aレセプターアンタゴニスト

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2008147306A Pending JP2008260776A (ja) 2001-11-30 2008-06-04 アデノシンA2aレセプターアンタゴニスト

Country Status (19)

Country Link
US (1) US6916811B2 (US07794700-20100914-C00152.png)
EP (1) EP1448565B1 (US07794700-20100914-C00152.png)
JP (2) JP4284182B2 (US07794700-20100914-C00152.png)
KR (1) KR20050044593A (US07794700-20100914-C00152.png)
CN (1) CN1692116A (US07794700-20100914-C00152.png)
AR (1) AR037680A1 (US07794700-20100914-C00152.png)
AT (1) ATE453647T1 (US07794700-20100914-C00152.png)
AU (1) AU2002346503A1 (US07794700-20100914-C00152.png)
CA (1) CA2468649C (US07794700-20100914-C00152.png)
DE (1) DE60234951D1 (US07794700-20100914-C00152.png)
ES (1) ES2336435T3 (US07794700-20100914-C00152.png)
HK (1) HK1063780A1 (US07794700-20100914-C00152.png)
HU (1) HUP0402018A3 (US07794700-20100914-C00152.png)
IL (1) IL161716A0 (US07794700-20100914-C00152.png)
MX (1) MXPA04005209A (US07794700-20100914-C00152.png)
PE (1) PE20030665A1 (US07794700-20100914-C00152.png)
TW (1) TW200306837A (US07794700-20100914-C00152.png)
WO (1) WO2003048165A1 (US07794700-20100914-C00152.png)
ZA (1) ZA200404161B (US07794700-20100914-C00152.png)

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MY132006A (en) * 2000-05-26 2007-09-28 Schering Corp ADENOSINE A2a RECEPTOR ANTAGONISTS
US6964288B2 (en) * 2001-07-06 2005-11-15 Ksaria Corporation Apparatus and method for automated preparation of an optical fiber
MXPA04003474A (es) 2001-10-15 2004-07-30 Schering Corp Imidazo (4,3-e)-1,2,4-triazolo(1,5-c) pirimidinas como antagonistas del receptor de adenosina a2a.
WO2003101455A2 (en) * 2002-05-30 2003-12-11 King Pharmaceuticals Research & Development, Inc. Pharmaceutically active compounds having a tricyclic pyrazolotriazolopyrimidine ring structure and methods of use
EP2295047A3 (en) * 2002-12-19 2011-05-18 Schering Corporation Use of adenosine A2a receptor antagonists for the treatment of restless leg syndrome and other movement disorders
EP1678168B1 (en) * 2003-10-24 2012-07-11 Exelixis, Inc. P70s6 kinase modulators and method of use
EP1678182B1 (en) * 2003-10-28 2007-02-07 Schering Corporation Process for preparing substituted 5-amino-pyrazolo- [4,3-e]-1,2,4-triazolo [1,5-c]pyrimidines
BRPI0417205A (pt) * 2003-12-19 2007-02-06 Schering Corp composições farmacêuticas
ES2385702T3 (es) * 2005-06-07 2012-07-30 Kyowa Hakko Kirin Co., Ltd. Antagonistas de A2A para uso en el tratamiento de trastornos de la motricidad
ES2273599B1 (es) 2005-10-14 2008-06-01 Universidad De Barcelona Compuestos para el tratamiento de la fibrilacion auricular.
PE20080145A1 (es) * 2006-03-21 2008-02-11 Janssen Pharmaceutica Nv Tetrahidro-pirimidoazepinas como moduladores de trpv1
US7723343B2 (en) * 2007-03-30 2010-05-25 King Pharmaceuticals Research And Development, Inc. Adenosine A2A receptor antagonists
PE20091102A1 (es) 2007-12-17 2009-07-25 Janssen Pharmaceutica Nv Moduladores imidazolo-, oxazolo-, y tiazolopirimidina del trpv1
US20100203165A1 (en) * 2008-08-01 2010-08-12 Gerald Horn Compositions and methods for treatment of disorders or conditions of the eye
US20100029662A1 (en) 2008-08-01 2010-02-04 Alpha Synergy Development, Inc. Vasoconstriction compositions and methods of use
US8952011B2 (en) 2008-08-01 2015-02-10 Eye Therapies Llc Compositions and methods for the treatment of nasal conditions
AU2009335019A1 (en) 2008-12-30 2011-08-18 Arqule, Inc. Substituted 1H-pyrazolo[3,4-d]pyrimidine-6-amine compounds
AU2010232727A1 (en) 2009-03-31 2011-10-20 Arqule, Inc. Substituted heterocyclic compounds
US8987270B2 (en) 2009-07-27 2015-03-24 Eye Therapies Llc Formulations of selective alpha-2 agonists and methods of use thereof
CA2782872A1 (en) * 2009-12-17 2011-06-23 Alpha Synergy Development, Inc. Compositions and methods for ophthalmic delivery of nasal decongestants
US8445526B2 (en) 2011-02-03 2013-05-21 Glaucoma & Nasal Therapies Llc Compositions and methods for treatment of glaucoma
US8999938B2 (en) 2013-06-21 2015-04-07 Gnt Llc Ophthalmic lipophilic drug delivery vehicle formulations
CN110742893B (zh) * 2018-07-23 2024-04-05 百济神州(北京)生物科技有限公司 A2a受体拮抗剂治疗癌症的方法
KR102653800B1 (ko) 2018-11-30 2024-04-01 머크 샤프 앤드 돔 엘엘씨 아데노신 수용체 길항제로서의 9-치환된 아미노 트리아졸로 퀴나졸린 유도체, 제약 조성물 및 그의 용도
DE102019116986A1 (de) 2019-06-24 2020-12-24 Helmholtz-Zentrum Dresden-Rossendorf E. V. Deuterierte 7-(3-(4-(2-([18F]Fluor)ethoxy)phenyl)propyl)-2-(furan-2-yl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amin-Derivate
EP3999513A4 (en) * 2019-07-17 2022-12-21 Teon Therapeutics, Inc. ADENOSINE A2A RECEPTOR ANTAGONISTS AND THEIR USES
CN111825698B (zh) 2019-07-30 2021-10-15 杭州阿诺生物医药科技有限公司 腺苷受体拮抗剂
CN112608316B (zh) 2019-07-30 2022-10-21 厦门宝太生物科技股份有限公司 一种吡唑并三嗪类腺苷受体拮抗剂

Family Cites Families (9)

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Publication number Priority date Publication date Assignee Title
IT1264901B1 (it) 1993-06-29 1996-10-17 Schering Plough S P A Analoghi eterociclici di 1,2,4-triazolo(15-c)pirimidine ad attivita' antagonista per il recettore a2 dell'adenosina
EP0666079B1 (en) * 1993-07-27 2001-11-07 Kyowa Hakko Kogyo Co., Ltd. Remedy for parkinson's disease
IT1277392B1 (it) * 1995-07-28 1997-11-10 Schering Plough S P A Analoghi eterociclici di 1,2,4-triazolo(1,5-c]pirimidine ad attivita' antagonista per il recettore a2a dell'adenosina
IT1291372B1 (it) 1997-05-21 1999-01-07 Schering Plough S P A Uso di analoghi eterociclici di 1,2,4-triazolo (1,5-c) pirimidine per la preparazione di medicamenti utili per il trattamento delle malattie
US6921825B2 (en) * 1998-09-16 2005-07-26 King Pharmaceuticuals Research & Development, Inc. Adenosine A3 receptor modulators
US6448253B1 (en) 1998-09-16 2002-09-10 King Pharmaceuticals Research And Development, Inc. Adenosine A3 receptor modulators
MY132006A (en) * 2000-05-26 2007-09-28 Schering Corp ADENOSINE A2a RECEPTOR ANTAGONISTS
WO2003101455A2 (en) * 2002-05-30 2003-12-11 King Pharmaceuticals Research & Development, Inc. Pharmaceutically active compounds having a tricyclic pyrazolotriazolopyrimidine ring structure and methods of use
AR044041A1 (es) * 2003-04-23 2005-08-24 Schering Corp Antagonistas del receptor a2a de 2-alquinil- y 2-alquenil-pirazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pirimidina adenosina

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