ATE293599T1 - Indolderivate als faktor xa inhibitoren - Google Patents
Indolderivate als faktor xa inhibitorenInfo
- Publication number
- ATE293599T1 ATE293599T1 AT98965244T AT98965244T ATE293599T1 AT E293599 T1 ATE293599 T1 AT E293599T1 AT 98965244 T AT98965244 T AT 98965244T AT 98965244 T AT98965244 T AT 98965244T AT E293599 T1 ATE293599 T1 AT E293599T1
- Authority
- AT
- Austria
- Prior art keywords
- inhibitors
- factor
- indole derivatives
- indole
- derivatives
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP97122901 | 1997-12-24 | ||
PCT/EP1998/008030 WO1999033800A1 (en) | 1997-12-24 | 1998-12-10 | Indole derivatives as inhibitors or factor xa |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE293599T1 true ATE293599T1 (de) | 2005-05-15 |
Family
ID=8227884
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT98965244T ATE293599T1 (de) | 1997-12-24 | 1998-12-10 | Indolderivate als faktor xa inhibitoren |
Country Status (29)
Country | Link |
---|---|
US (1) | US6337344B1 (de) |
EP (1) | EP1042287B1 (de) |
JP (1) | JP4589529B2 (de) |
KR (1) | KR100608472B1 (de) |
CN (1) | CN1220681C (de) |
AR (1) | AR018031A1 (de) |
AT (1) | ATE293599T1 (de) |
AU (1) | AU743881B2 (de) |
BR (1) | BR9814340B1 (de) |
CA (1) | CA2316172C (de) |
CZ (1) | CZ298827B6 (de) |
DE (1) | DE69829879T2 (de) |
DK (1) | DK1042287T3 (de) |
ES (1) | ES2241194T3 (de) |
HK (1) | HK1033795A1 (de) |
HU (1) | HU227568B1 (de) |
ID (1) | ID27044A (de) |
IL (1) | IL136954A0 (de) |
MY (1) | MY120064A (de) |
NO (1) | NO316912B1 (de) |
NZ (1) | NZ505370A (de) |
PL (1) | PL195682B1 (de) |
PT (1) | PT1042287E (de) |
RU (1) | RU2225397C2 (de) |
SI (1) | SI1042287T1 (de) |
TR (1) | TR200001954T2 (de) |
TW (1) | TWI241294B (de) |
WO (1) | WO1999033800A1 (de) |
ZA (1) | ZA9811759B (de) |
Families Citing this family (71)
Publication number | Priority date | Publication date | Assignee | Title |
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GB9716657D0 (en) | 1997-08-07 | 1997-10-15 | Zeneca Ltd | Chemical compounds |
DE69829879T2 (de) * | 1997-12-24 | 2006-03-02 | Sanofi-Aventis Deutschland Gmbh | Indolderivate als faktor xa inhibitoren |
GB9803226D0 (en) | 1998-02-17 | 1998-04-08 | Zeneca Ltd | Chemical compounds |
DE19917504A1 (de) * | 1999-04-17 | 2000-10-19 | Dresden Arzneimittel | Verwendung von Hydroxyindolen, die Inhibitoren der Phosphodiesterase 4 sind, zur Therapie chronisch obstruktiver Lungenerkrankungen |
WO2000040571A1 (en) | 1999-01-02 | 2000-07-13 | Aventis Pharma Deutschland Gmbh | Novel malonic acid derivatives, processes for their preparation, their use and pharmaceutical compositions containing them (inhibition of factor xa activity) |
IL144095A0 (en) | 1999-01-02 | 2002-05-23 | Aventis Pharma Gmbh | Arylalkanoyl derivatives, processes for their preparation, their use and pharmaceutical compositions containing them |
GB9902461D0 (en) * | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
GB9902455D0 (en) * | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
GB9902459D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
GB9902453D0 (en) * | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
GB9902452D0 (en) * | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
AR024158A1 (es) * | 1999-06-01 | 2002-09-04 | Smithkline Beecham Corp | Compuestos antibacterianos |
EP1095933A1 (de) | 1999-10-30 | 2001-05-02 | Aventis Pharma Deutschland GmbH | N-Guanidinoalkylamide, Verfahren zu ihrer Herstellung, ihre Verwendung und pharmazeutische Zusammensetzungen, die sie enthalten |
GB0000625D0 (en) | 2000-01-13 | 2000-03-01 | Zeneca Ltd | Chemical compounds |
EP1127884A1 (de) | 2000-02-26 | 2001-08-29 | Aventis Pharma Deutschland GmbH | Neue Malonsäure Derivaie, Verfahren zu ihrer Herstellung, ihre Verwendung als Inhibitor der Faktor XA Aktivtät und pharmazeutische Zusammensetzungen diese enthaltend |
GB0005366D0 (en) * | 2000-03-06 | 2000-04-26 | Xenova Ltd | Pharmaceutical compounds |
EP1272483A2 (de) * | 2000-03-24 | 2003-01-08 | Millenium Pharmaceuticals, Inc. | Oxindole als faktor xa inhibitoren |
AU2001271531A1 (en) * | 2000-06-27 | 2002-01-08 | Smith Kline Beecham Corporation | Fatty acid synthase inhibitors |
WO2002026712A2 (en) * | 2000-09-29 | 2002-04-04 | Millennium Pharmaceuticals, Inc. | Quaternary amines and related inhibitors of factor xa |
TNSN03146A1 (fr) | 2001-06-28 | 2005-12-23 | Pfizer Prod Inc | Indoles, benzofurannes et benzothiophenes a substituant triamide, utiles comme inhibiteurs de secretion de la proteine de transfert des triglycerides microsomaux et/ou de l'apolipo-proteine b (apo b). |
DE10147672A1 (de) * | 2001-09-27 | 2003-04-10 | Bayer Ag | Substituierte 2,5-Diamidoindole und ihre Verwendung |
EP1314733A1 (de) | 2001-11-22 | 2003-05-28 | Aventis Pharma Deutschland GmbH | Indol-2-carbonsäureamide als Faktor-Xa-Hemmer |
CA2477604A1 (en) | 2002-03-13 | 2003-09-25 | Signum Biosciences, Inc. | Modulation of protein methylation and phosphoprotein phosphate |
WO2004050637A2 (en) | 2002-12-03 | 2004-06-17 | Axys Pharmaceuticals, Inc. | 2-(2-hydroxybiphenyl-3-yl)-1h-benzoimidazole-5-carboxamidine derivatives as factor viia inhibitors |
EP1479677A1 (de) * | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Neue Indolderivate als Faktor Xa-Inhibitoren |
US7317027B2 (en) * | 2003-05-19 | 2008-01-08 | Sanofi-Aventis Deutschland Gmbh | Azaindole-derivatives as factor Xa inhibitors |
EP1479680A1 (de) * | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Azaindole-Derivative als Faktor Xa Hemmer |
WO2004108671A1 (en) * | 2003-06-06 | 2004-12-16 | Suven Life Sciences Limited | Substituted indoles with serotonin receptor affinity, process for their preparation and pharmaceutical compositions containing them |
SE0302035D0 (sv) * | 2003-07-09 | 2003-07-09 | Biolipox Ab | New compound |
US7348338B2 (en) * | 2003-07-17 | 2008-03-25 | Plexxikon, Inc. | PPAR active compounds |
UA88767C2 (uk) * | 2003-07-17 | 2009-11-25 | Плексікон, Інк. | Ppar активні сполуки |
US7186084B2 (en) * | 2003-11-19 | 2007-03-06 | General Electric Company | Hot gas path component with mesh and dimpled cooling |
EP1568698A1 (de) * | 2004-02-27 | 2005-08-31 | Aventis Pharma Deutschland GmbH | Pyrrolderivate als faktor-xa-inhibitoren |
US7705023B2 (en) | 2004-06-18 | 2010-04-27 | Biolipox Ab | Indoles useful in the treatment of inflammation |
EP1765775B1 (de) * | 2004-06-18 | 2009-04-29 | Biolipox AB | Zur behandlung von entzündungen geeignete indole |
MXPA06014536A (es) * | 2004-06-18 | 2007-06-05 | Biolipox Ab | Indoles utiles en el tratamiento de inflamacion. |
WO2006027135A1 (en) * | 2004-09-06 | 2006-03-16 | F. Hoffmann-La Roche Ag | 4-aminomethyl benzamidine derivatives and their use as factor viiia inhibitors |
AU2005299693B2 (en) | 2004-10-26 | 2012-07-05 | Janssen Pharmaceutica, N.V. | Factor Xa compounds |
GB0428173D0 (en) * | 2004-12-23 | 2005-01-26 | Astrazeneca Ab | Compounds |
FR2880625B1 (fr) * | 2005-01-07 | 2007-03-09 | Sanofi Aventis Sa | Derives de n-(heteroaryl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique |
US20100197687A1 (en) * | 2005-01-19 | 2010-08-05 | Benjamin Pelcman | Indoles Useful in the Treatment of Inflammation |
US20090048285A1 (en) * | 2005-01-19 | 2009-02-19 | Benjamin Pelcman | Pyrrolopyridines Useful in the Treatment of Inflammation |
EP1838669A1 (de) * | 2005-01-19 | 2007-10-03 | Biolipox AB | Entzündungshemmende indol-derivate |
US20090069384A1 (en) * | 2005-01-19 | 2009-03-12 | Biolipox Ab | Thienopyrroles useful in the treatment of inflammation |
CA2594878A1 (en) * | 2005-01-19 | 2006-07-27 | Biolipox Ab | Indoles useful in the treatment of inflammation |
MX2007008759A (es) | 2005-01-19 | 2007-09-11 | Biolipox Ab | Indoles utiles en el tratamiento de la inflamacion. |
CA2601777A1 (en) * | 2005-02-03 | 2006-08-10 | Signum Biosciences, Inc. | Compositions and methods for enhancing cognitive function |
US7923041B2 (en) | 2005-02-03 | 2011-04-12 | Signum Biosciences, Inc. | Compositions and methods for enhancing cognitive function |
EP1747779A1 (de) | 2005-07-28 | 2007-01-31 | Laboratorios Del Dr. Esteve, S.A. | Tetrahydro-b-carbolinsulfonamid-Derivate als 5-HT6 Liganden |
NZ567162A (en) * | 2005-09-07 | 2011-06-30 | Plexxikon Inc | 1, 3-disubstituted indole derivatives for use as PPAR modulators |
US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
GB2431927B (en) | 2005-11-04 | 2010-03-17 | Amira Pharmaceuticals Inc | 5-Lipoxygenase-activating protein (FLAP) inhibitors |
JP5322935B2 (ja) | 2006-07-31 | 2013-10-23 | アクティベサイト ファーマシューティカルズ インコーポレイティッド | 血漿カリクレインの阻害薬 |
AU2007297013B2 (en) * | 2006-09-13 | 2012-05-31 | Sanofi-Aventis | Isoserine derivatives for use as coagulation factor IXa inhibitors |
ES2452343T3 (es) * | 2006-09-29 | 2014-04-01 | Glaxosmithkline Llc | Compuestos de indol sustituidos |
CN101535253A (zh) | 2006-11-09 | 2009-09-16 | 弗·哈夫曼-拉罗切有限公司 | 吲哚和苯并呋喃2-甲酰胺衍生物 |
US8524917B2 (en) | 2007-01-11 | 2013-09-03 | Allergan, Inc. | 6-substituted indole-3-carboxylic acid amide compounds having sphingosine-1-phosphate (S1P) receptor antagonist biological activity |
PE20090159A1 (es) * | 2007-03-08 | 2009-02-21 | Plexxikon Inc | COMPUESTOS DERIVADOS DE ACIDO INDOL-PROPIONICO COMO MODULADORES PPARs |
NZ582056A (en) * | 2007-08-10 | 2012-08-31 | Lundbeck & Co As H | Bicyclic heteroaryl compounds for treating conditions related to p2x7 receptor activation |
AU2009239430B2 (en) | 2008-04-21 | 2015-01-22 | Signum Biosciences, Inc. | Compounds, compositions and methods for making the same |
CN101654427B (zh) * | 2008-08-19 | 2012-12-05 | 信谊药厂 | 抗凝化合物、组合物及其用途 |
WO2011044134A1 (en) | 2009-10-05 | 2011-04-14 | Albany Molecular Research, Inc. | Epiminocycloalkyl(b)indole derivatives as serotonin sub-type 6 (5-ht6) modulators and uses thereof |
US9206123B2 (en) | 2009-12-18 | 2015-12-08 | Activesite Pharmaceuticals, Inc. | Prodrugs of inhibitors of plasma kallikrein |
SG10201408429UA (en) | 2009-12-18 | 2015-02-27 | Activesite Pharmaceuticals Inc | Prodrugs of inhibitors of plasma kallikrein |
EP2668191A4 (de) | 2011-01-19 | 2014-08-20 | Albany Molecular Res Inc | Benzofuro-[3,2-c-]pyridine und verwandte analoga als serotonin-untertyp-6 (5-ht6)-modulatoren zur behandlung von adipositas, stoffwechselsyndrom, kognition und schizophrenie |
US9353113B2 (en) | 2011-03-18 | 2016-05-31 | Ono Pharmaceutical Co., Ltd. | Tetrahydrocarboline derivative |
US8691861B2 (en) | 2011-04-13 | 2014-04-08 | Activesite Pharmaceuticals, Inc. | Prodrugs of inhibitors of plasma kallikrein |
WO2017123826A1 (en) | 2016-01-14 | 2017-07-20 | Beth Israel Deaconess Medical Center, Inc. | Mast-cell modulators and uses thereof |
ES2910787T3 (es) | 2016-05-12 | 2022-05-13 | Univ Michigan Regents | Inhibidores de ASH1L y métodos de tratamiento con los mismos |
CN111655257A (zh) * | 2017-11-10 | 2020-09-11 | 密歇根大学董事会 | Ash1l抑制剂及用其进行治疗的方法 |
WO2023068700A1 (ko) * | 2021-10-20 | 2023-04-27 | 동국대학교 와이즈캠퍼스 산학협력단 | 두룸아마이드 a를 포함하는 혈소판 응집 예방, 개선 또는 치료용 조성물 |
Family Cites Families (11)
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US4529724A (en) * | 1983-10-11 | 1985-07-16 | Mcneilab, Inc. | 6H-indolo[2,1-c][1,4]benzodiazepines and 12-oxo derivatives useful as antihypertensives |
DD235866B1 (de) | 1985-03-29 | 1988-12-28 | Univ Leipzig | Verfahren zur herstellung von n alpha (2-naphthyl)-sulfonylaminoacylierten amidinophenylalanisamiden |
AU707653B2 (en) | 1994-04-26 | 1999-07-15 | Selectide Corporation | Factor Xa inhibitors |
US5612363A (en) * | 1995-06-02 | 1997-03-18 | Berlex Laboratories, Inc. | N,N-di(aryl) cyclic urea derivatives as anti-coagulants |
DE19530996A1 (de) | 1995-08-23 | 1997-02-27 | Boehringer Mannheim Gmbh | Cyclische Guanidine, Verfahren zu ihrer Herstellung und Arzneimittel |
US5849759A (en) * | 1995-12-08 | 1998-12-15 | Berlex Laboratories, Inc. | Naphthyl-substituted benzimidazole derivatives as anti-coagulants |
CA2244851A1 (en) * | 1996-02-22 | 1997-08-28 | Petrus Fredericus Wilhelmus Stouten | M-amidino phenyl analogs as factor xa inhibitors |
US6200969B1 (en) * | 1996-09-12 | 2001-03-13 | Idun Pharmaceuticals, Inc. | Inhibition of apoptosis using interleukin-1β-converting enzyme (ICE)/CED-3 family inhibitors |
US6184244B1 (en) * | 1996-12-16 | 2001-02-06 | Idun Pharmaceuticals, Inc. | C-terminal modified (N-substituted)-2-indolyl dipeptides as inhibitors of the ICE/ced-3 family of cysteine proteases |
US5886191A (en) * | 1997-08-18 | 1999-03-23 | Dupont Pharmaceuticals Company | Amidinoindoles, amidinoazoles, and analogs thereof |
DE69829879T2 (de) * | 1997-12-24 | 2006-03-02 | Sanofi-Aventis Deutschland Gmbh | Indolderivate als faktor xa inhibitoren |
-
1998
- 1998-12-10 DE DE69829879T patent/DE69829879T2/de not_active Expired - Lifetime
- 1998-12-10 ES ES98965244T patent/ES2241194T3/es not_active Expired - Lifetime
- 1998-12-10 WO PCT/EP1998/008030 patent/WO1999033800A1/en active IP Right Grant
- 1998-12-10 DK DK98965244T patent/DK1042287T3/da active
- 1998-12-10 SI SI9830771T patent/SI1042287T1/xx unknown
- 1998-12-10 BR BRPI9814340-9A patent/BR9814340B1/pt not_active IP Right Cessation
- 1998-12-10 KR KR1020007007084A patent/KR100608472B1/ko not_active IP Right Cessation
- 1998-12-10 ID IDW20001225A patent/ID27044A/id unknown
- 1998-12-10 PL PL98341400A patent/PL195682B1/pl not_active IP Right Cessation
- 1998-12-10 PT PT98965244T patent/PT1042287E/pt unknown
- 1998-12-10 JP JP2000526484A patent/JP4589529B2/ja not_active Expired - Fee Related
- 1998-12-10 TR TR2000/01954T patent/TR200001954T2/xx unknown
- 1998-12-10 CN CNB988126532A patent/CN1220681C/zh not_active Expired - Fee Related
- 1998-12-10 CZ CZ20002310A patent/CZ298827B6/cs not_active IP Right Cessation
- 1998-12-10 NZ NZ505370A patent/NZ505370A/en not_active IP Right Cessation
- 1998-12-10 CA CA002316172A patent/CA2316172C/en not_active Expired - Fee Related
- 1998-12-10 HU HU0100723A patent/HU227568B1/hu not_active IP Right Cessation
- 1998-12-10 AU AU20528/99A patent/AU743881B2/en not_active Ceased
- 1998-12-10 IL IL13695498A patent/IL136954A0/xx not_active IP Right Cessation
- 1998-12-10 AT AT98965244T patent/ATE293599T1/de active
- 1998-12-10 US US09/582,344 patent/US6337344B1/en not_active Expired - Lifetime
- 1998-12-10 RU RU2000119774/04A patent/RU2225397C2/ru not_active IP Right Cessation
- 1998-12-10 EP EP98965244A patent/EP1042287B1/de not_active Expired - Lifetime
- 1998-12-22 AR ARP980106607A patent/AR018031A1/es active IP Right Grant
- 1998-12-22 ZA ZA9811759A patent/ZA9811759B/xx unknown
- 1998-12-23 MY MYPI98005870A patent/MY120064A/en unknown
-
1999
- 1999-02-23 TW TW087121374A patent/TWI241294B/zh not_active IP Right Cessation
-
2000
- 2000-06-14 NO NO20003057A patent/NO316912B1/no not_active IP Right Cessation
-
2001
- 2001-06-21 HK HK01104324A patent/HK1033795A1/xx not_active IP Right Cessation
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