JP2000514801A5 - - Google Patents

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Publication number
JP2000514801A5
JP2000514801A5 JP1998505247A JP50524798A JP2000514801A5 JP 2000514801 A5 JP2000514801 A5 JP 2000514801A5 JP 1998505247 A JP1998505247 A JP 1998505247A JP 50524798 A JP50524798 A JP 50524798A JP 2000514801 A5 JP2000514801 A5 JP 2000514801A5
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JP
Japan
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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JP1998505247A
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English (en)
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JP2000514801A (ja
JP4202421B2 (ja
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Priority claimed from PCT/US1997/011320 external-priority patent/WO1998001426A1/en
Publication of JP2000514801A publication Critical patent/JP2000514801A/ja
Publication of JP2000514801A5 publication Critical patent/JP2000514801A5/ja
Application granted granted Critical
Publication of JP4202421B2 publication Critical patent/JP4202421B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
Figure 2000514801
JP50524798A 1996-07-08 1997-07-01 抗高血圧、心臓保護、抗乏血及び抗脂肪分解特性を有する化合物 Expired - Fee Related JP4202421B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US2136696P 1996-07-08 1996-07-08
US60/021,366 1996-07-08
PCT/US1997/011320 WO1998001426A1 (en) 1996-07-08 1997-07-01 Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties

Publications (3)

Publication Number Publication Date
JP2000514801A JP2000514801A (ja) 2000-11-07
JP2000514801A5 true JP2000514801A5 (ja) 2005-03-10
JP4202421B2 JP4202421B2 (ja) 2008-12-24

Family

ID=21803790

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50524798A Expired - Fee Related JP4202421B2 (ja) 1996-07-08 1997-07-01 抗高血圧、心臓保護、抗乏血及び抗脂肪分解特性を有する化合物

Country Status (22)

Country Link
EP (1) EP0912520B1 (ja)
JP (1) JP4202421B2 (ja)
KR (1) KR20000023635A (ja)
CN (1) CN1228770A (ja)
AP (1) AP903A (ja)
AT (1) ATE239725T1 (ja)
AU (1) AU746590B2 (ja)
BG (1) BG103135A (ja)
BR (1) BR9710156A (ja)
CA (1) CA2259538C (ja)
CZ (1) CZ291785B6 (ja)
DE (1) DE69721776T2 (ja)
EA (1) EA001801B1 (ja)
ES (1) ES2199365T3 (ja)
HU (1) HUP9903815A3 (ja)
IL (1) IL127890A0 (ja)
NO (1) NO313671B1 (ja)
OA (1) OA10953A (ja)
PL (1) PL331036A1 (ja)
SK (1) SK2299A3 (ja)
UA (1) UA51716C2 (ja)
WO (1) WO1998001426A1 (ja)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6376472B1 (en) * 1996-07-08 2002-04-23 Aventis Pharmaceuticals, Inc. Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
GB9723590D0 (en) 1997-11-08 1998-01-07 Glaxo Group Ltd Chemical compounds
YU44900A (sh) 1998-01-31 2003-01-31 Glaxo Group Limited Derivati 2-(purin-9-il)tetrahidrofuran-3,4-diola
GB9813554D0 (en) 1998-06-23 1998-08-19 Glaxo Group Ltd Chemical compounds
KR20010071591A (ko) 1998-06-23 2001-07-28 그레이엄 브레레톤, 레슬리 에드워즈 2-(퓨린-9-일)-테트라히드로푸란-3,4-디올 유도체
WO2000030638A1 (fr) * 1998-11-25 2000-06-02 Daiichi Radioisotope Laboratories, Ltd. Medicaments ou reactifs contenant des composes cycloalkyl n-acyloxyles
ATE275565T1 (de) 1998-12-31 2004-09-15 Aventis Pharma Inc Verfahren zur herstellung von n6-substituierten deaza-adenosinderivaten
GB0106867D0 (en) * 2001-03-20 2001-05-09 Glaxo Group Ltd Process
US20030069423A1 (en) * 2001-05-10 2003-04-10 Ayers Timothy A. Novel processes for the preparation of adenosine compounds and intermediates thereto
EP1258247A1 (en) * 2001-05-14 2002-11-20 Aventis Pharma Deutschland GmbH Adenosine analogues for the treatment of insulin resistance syndrome and diabetes
FR2835186B1 (fr) 2002-01-28 2006-10-20 Aventis Pharma Sa Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
HUP0200849A2 (hu) * 2002-03-06 2004-08-30 Sanofi-Synthelabo N-aminoacetil-2-ciano-pirrolidin-származékok, e vegyületeket tartalmazó gyógyszerkészítmények és eljárás előállításukra
EP1375508A1 (en) * 2002-06-27 2004-01-02 Aventis Pharma Deutschland GmbH N6-substituted adenosine analogues and their use as pharmaceutical agents
US7163937B2 (en) 2003-08-21 2007-01-16 Bristol-Myers Squibb Company Cyclic derivatives as modulators of chemokine receptor activity
FR2862969A1 (fr) * 2003-11-28 2005-06-03 Oreal Procede de preparation de derives paraphenylenediamine a groupement pyrrolidinyle, substitue par un radical azote, et composes intermediaires
EP1574508A1 (de) 2004-01-30 2005-09-14 Lonza AG Verfahren zur Herstellung von Acetalen und Ketalen von 3-Amino-5-(hydroxymethyl)-cyclopentan-1,2-diolen, sowie deren Derivaten und Salzen
PE20060272A1 (es) 2004-05-24 2006-05-22 Glaxo Group Ltd (2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a
JP2006022045A (ja) * 2004-07-08 2006-01-26 Kaneka Corp 光学活性1−t−ブトキシカルボニル−3−アミノピロリジン塩の単離精製方法
GB0514809D0 (en) 2005-07-19 2005-08-24 Glaxo Group Ltd Compounds
US7629351B2 (en) 2006-07-28 2009-12-08 Bristol-Myers Squibb Company N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-2-oxo-3-(6-(trifluoromethyl)quinazolin-4-ylamino) pyrrolidin-1-yl)cyclohexyl)acetamide and other modulators of chemokine receptor activity, crystalline forms and process
US7671062B2 (en) 2006-07-28 2010-03-02 Bristol-Myers Squibb Company Modulators of chemokine receptor activity, crystalline forms and process
US7687508B2 (en) 2006-07-28 2010-03-30 Bristol-Myers Squibb Company Cyclic derivatives as modulators of chemokine receptor activity
DE102007002260A1 (de) 2007-01-16 2008-07-31 Sanofi-Aventis Verwendung von substituierten Pyranonsäurederivaten zur Herstellung von Medikamenten zur Behandlung des Metabolischen Syndroms
US8383812B2 (en) 2009-10-13 2013-02-26 Bristol-Myers Squibb Company N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-3-(7-tert-butylpyrazolo[1,5-A][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin-1-yl)cyclohexyl)acetamide, a dual modulator of chemokine receptor activity, crystalline forms and processes
BR112018014525A2 (pt) * 2016-01-14 2018-12-11 Handok Inc compostos que antagonizam receptor de adenosina a3, método para preparação dos mesmos e aplicação médica dos mesmos
CN110627765B (zh) * 2019-10-14 2021-08-20 浙江乐普药业股份有限公司 一种替卡格雷关键中间体的制备方法
CN112047919B (zh) * 2020-09-16 2021-06-18 常州制药厂有限公司 一种替卡格雷中间体及其制备方法
KR102308854B1 (ko) * 2021-02-26 2021-10-05 퓨쳐메디신 주식회사 카보사이클릭 뉴클레오사이드 유도체를 포함하는 코로나바이러스감염증-19 예방 및 치료용 약학적 조성물

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2095960T3 (es) * 1990-09-25 1997-03-01 Rhone Poulenc Rorer Int Compuestos que tienen propiedades antihipertensivas y antiisquemicas.
US5561134A (en) * 1990-09-25 1996-10-01 Rhone-Poulenc Rorer Pharmaceuticals Inc. Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties
WO1995018817A1 (fr) * 1994-01-07 1995-07-13 Laboratoires Upsa Nouveaux derives de l'adenosine, leurs procedes de preparation, compositions pharmaceutiques les contenant
US5554746A (en) * 1994-05-16 1996-09-10 Isis Pharmaceuticals, Inc. Lactam nucleic acids

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