IL163996A0 - N3 alkylated benzimidazole derivatives as mek inhibitors - Google Patents
N3 alkylated benzimidazole derivatives as mek inhibitorsInfo
- Publication number
- IL163996A0 IL163996A0 IL16399603A IL16399603A IL163996A0 IL 163996 A0 IL163996 A0 IL 163996A0 IL 16399603 A IL16399603 A IL 16399603A IL 16399603 A IL16399603 A IL 16399603A IL 163996 A0 IL163996 A0 IL 163996A0
- Authority
- IL
- Israel
- Prior art keywords
- benzimidazole derivatives
- mek inhibitors
- alkylated benzimidazole
- alkylated
- mek
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
- C07D403/06—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 only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US36416402P | 2002-03-13 | 2002-03-13 | |
PCT/US2003/007565 WO2003077855A2 (fr) | 2002-03-13 | 2003-03-13 | Derives de benzimidazole n3 alkyles servant d'inhibiteurs de mek |
Publications (1)
Publication Number | Publication Date |
---|---|
IL163996A0 true IL163996A0 (en) | 2005-12-18 |
Family
ID=28041882
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL16399603A IL163996A0 (en) | 2002-03-13 | 2003-03-13 | N3 alkylated benzimidazole derivatives as mek inhibitors |
Country Status (18)
Country | Link |
---|---|
US (2) | US20030216460A1 (fr) |
EP (1) | EP1482944A4 (fr) |
JP (1) | JP2005526076A (fr) |
KR (1) | KR20040098013A (fr) |
CN (1) | CN1652792A (fr) |
AR (1) | AR038972A1 (fr) |
AU (1) | AU2003220202A1 (fr) |
CA (1) | CA2478534A1 (fr) |
CO (1) | CO5611145A2 (fr) |
DO (1) | DOP2003000614A (fr) |
IL (1) | IL163996A0 (fr) |
MX (1) | MXPA04008894A (fr) |
PA (1) | PA8569201A1 (fr) |
PL (1) | PL378635A1 (fr) |
RU (1) | RU2300528C2 (fr) |
TW (1) | TW200406203A (fr) |
UA (1) | UA76837C2 (fr) |
WO (1) | WO2003077855A2 (fr) |
Families Citing this family (72)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT3000810T (pt) * | 2002-03-13 | 2017-10-25 | Array Biopharma Inc | Derivados de benzimidazole alquilado n3 como inibidores de mek |
US7235537B2 (en) * | 2002-03-13 | 2007-06-26 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as MEK inhibitors |
DE602004023207D1 (de) * | 2003-07-24 | 2009-10-29 | Warner Lambert Co | Benzimidazol-derivate als mek-hemmer |
US7538120B2 (en) * | 2003-09-03 | 2009-05-26 | Array Biopharma Inc. | Method of treating inflammatory diseases |
US7144907B2 (en) * | 2003-09-03 | 2006-12-05 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
NZ545864A (en) | 2003-09-22 | 2009-12-24 | S Bio Pte Ltd | Benzimidazole derivates: preparation and pharmaceutical applications |
JP4768628B2 (ja) * | 2003-11-19 | 2011-09-07 | アレイ バイオファーマ、インコーポレイテッド | Mekの二環系阻害剤及びその使用方法 |
US7732616B2 (en) * | 2003-11-19 | 2010-06-08 | Array Biopharma Inc. | Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof |
US7517994B2 (en) * | 2003-11-19 | 2009-04-14 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
AU2004293026B2 (en) | 2003-11-21 | 2012-01-19 | Array Biopharma Inc. | AKT protein kinase inhibitors |
EP1699477A2 (fr) * | 2003-12-11 | 2006-09-13 | Theravance, Inc. | Compositions a utiliser dans le traitement de maladies proliferatives cellulaires caracterisees par la presence d'une tyrosine kinase receptrice mutante |
KR101318012B1 (ko) | 2004-10-20 | 2013-10-14 | 메르크 세로노 에스.에이. | 3-아릴아미노 피리딘 유도체 |
WO2006058752A1 (fr) * | 2004-12-01 | 2006-06-08 | Laboratoires Serono S.A. | Dérivés de [1,2,4]triazolo[4,3-a]pyridine pour le traitement de maladies hyperproliférantes |
SG177981A1 (en) | 2005-05-18 | 2012-02-28 | Array Biopharma Inc | 4-(phenylamino)-6-oxo-1, 6-dihydropyridazine-3-carboxamide derivatives as mek inhibitors for the treatment of hyperproliferative diseases |
CA2612419C (fr) | 2005-06-23 | 2017-06-13 | Array Biopharma Inc. | Procede d'elaboration de composes benzimidazole |
US8101799B2 (en) | 2005-07-21 | 2012-01-24 | Ardea Biosciences | Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK |
PL1934174T3 (pl) * | 2005-10-07 | 2011-09-30 | Exelixis Inc | Azetydyny jako inhibitory w leczeniu chorób proliferacyjnych |
WO2007071951A1 (fr) * | 2005-12-21 | 2007-06-28 | Astrazeneca Ab | Sel de tosylate du 6-(4-bromo-2-chlorophenylamino)-7-fluoro-n-(2-hydroxyethoxy)-3-methyl-3h-benzimidazole-5-carboxamide, inhibiteur de mek pouvant etre employe dans le traitement du cancer |
GB0601962D0 (en) | 2006-01-31 | 2006-03-15 | Ucb Sa | Therapeutic agents |
DE602007011628D1 (de) | 2006-07-06 | 2011-02-10 | Array Biopharma Inc | Dihydrofuropyrimidine als akt-proteinkinaseinhibitoren |
US8063050B2 (en) | 2006-07-06 | 2011-11-22 | Array Biopharma Inc. | Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
UA99597C2 (ru) | 2006-07-06 | 2012-09-10 | Еррей Біофарма Інк. | Пиримидилциклопентаны как ингибиторы акт протеинкиназ |
WO2008006039A1 (fr) | 2006-07-06 | 2008-01-10 | Array Biopharma Inc. | Dihydrothiéno pyrimidines comme inhibiteurs de la protéine kinase akt |
ZA200901009B (en) * | 2006-08-21 | 2010-05-26 | Genentech Inc | Aza-benzothiophenyl compounds and methods of use |
ATE531720T1 (de) * | 2006-08-21 | 2011-11-15 | Genentech Inc | Aza-benzofuranylverbindungen und anwendungsverfahren dafür |
US7893085B2 (en) * | 2006-08-21 | 2011-02-22 | Genentech, Inc | Aza-benzothiophenyl compounds and methods of use |
CN101605540A (zh) | 2006-12-14 | 2009-12-16 | 埃克塞利希斯股份有限公司 | 使用mek抑制剂的方法 |
JO2985B1 (ar) | 2006-12-20 | 2016-09-05 | Takeda Pharmaceuticals Co | مثبطات كينازmapk/erk |
US8258152B2 (en) | 2007-06-12 | 2012-09-04 | Genentech, Inc. | N-substituted azaindoles and methods of use |
CA2692502C (fr) | 2007-07-05 | 2016-03-01 | Array Biopharma Inc. | Cyclopentanes de pyrimidyle comme inhibiteurs de proteines kinases akt |
US9409886B2 (en) | 2007-07-05 | 2016-08-09 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
US8846683B2 (en) | 2007-07-05 | 2014-09-30 | Array Biopharma, Inc. | Pyrimidyl cyclopentanes as Akt protein kinase inhibitors |
EP2173723B3 (fr) * | 2007-07-05 | 2014-11-19 | Array Biopharma Inc. | Pyrimidyl cyclopentanes utilsés comme inhibiteurs de la protéine kinase akt |
GB0714384D0 (en) | 2007-07-23 | 2007-09-05 | Ucb Pharma Sa | theraputic agents |
CA2705452C (fr) | 2007-11-12 | 2016-05-31 | Takeda Pharmaceutical Company Limited | Inhibiteurs de la mapk/erk kinase |
PE20091158A1 (es) | 2007-12-19 | 2009-08-28 | Genentech Inc | 5-anilinoimidazopiridinas y metodos de uso |
DK2231662T3 (da) | 2007-12-19 | 2011-08-29 | Genentech Inc | 8-Anilinoimidazopyridiner og deres anvendelse som anticancer- og/eller antiinflammatoriske midler |
AU2008340247B2 (en) * | 2007-12-21 | 2012-11-15 | Genentech, Inc. | Azaindolizines and methods of use |
WO2009089459A1 (fr) | 2008-01-09 | 2009-07-16 | Array Biopharma Inc. | Pyrimidylcyclopentanes hydroxylés utilisés comme inhibiteurs de protéine kinase akt |
KR101624752B1 (ko) * | 2008-01-09 | 2016-05-26 | 어레이 바이오파마 인크. | Akt 단백질 키나제 저해물질로써의 수산화된 피리미딜 시클로펜탄 |
EP2240494B1 (fr) | 2008-01-21 | 2016-03-30 | UCB Biopharma SPRL | Dérivés de thiénopyridine utilisés comme inhibiteurs de mek |
GB0811304D0 (en) | 2008-06-19 | 2008-07-30 | Ucb Pharma Sa | Therapeutic agents |
US8492427B2 (en) | 2008-07-01 | 2013-07-23 | Genentech, Inc. | Isoindolones derivatives as MEK kinase inhibitors and methods of use |
EP2310373A1 (fr) | 2008-07-01 | 2011-04-20 | Genentech, Inc. | Hétérocycles bicycliques en tant qu'inhibiteurs de mek kinase |
HUE027223T2 (en) | 2008-08-04 | 2016-08-29 | Merck Patent Gmbh | New Phenylamino Isonicotinamide Compounds |
WO2010051933A2 (fr) | 2008-11-10 | 2010-05-14 | Bayer Schering Pharma Aktiengesellschaft | Sulfonamido phénoxybenzamides substitués |
US9084781B2 (en) | 2008-12-10 | 2015-07-21 | Novartis Ag | MEK mutations conferring resistance to MEK inhibitors |
CA2777430A1 (fr) | 2009-10-21 | 2011-04-28 | Bayer Pharma Aktiengesellschaft | Benzosulfonamides substitues |
WO2011047796A1 (fr) | 2009-10-21 | 2011-04-28 | Bayer Schering Pharma Aktiengesellschaft | Dérivés d'halogénophénoxybenzamide substitués |
EP2491015A1 (fr) | 2009-10-21 | 2012-08-29 | Bayer Pharma Aktiengesellschaft | Benzosulfonamides substitués |
MX340392B (es) | 2010-02-25 | 2016-07-06 | Dana Farber Cancer Inst Inc | Mutaciones del protooncogen de serina/treonina-proteina cinasa b-raf (braf) que confieren resistencia a los inhibidores del protooncogen de serina/treonina-proteina cinasa b-raf. |
EA030276B1 (ru) | 2010-03-09 | 2018-07-31 | Дана-Фарбер Кэнсер Инститьют, Инк. | Способы идентификации страдающих раком пациентов и лечения рака у пациентов, у которых имеется или развивается резистентность к первой терапии рака |
US20130196990A1 (en) | 2010-10-06 | 2013-08-01 | Junya Qu | Benzimidazole Derivatives As PI3 Kinase Inhibitors |
JP2013542214A (ja) | 2010-10-29 | 2013-11-21 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 置換フェノキシピリジン類 |
TR201815685T4 (tr) | 2011-04-01 | 2018-11-21 | Genentech Inc | Kanser tedavisi için akt ve mek inhibe edici bileşiklerin kombinasyonları. |
CA2844699C (fr) | 2011-04-01 | 2019-05-07 | Genentech, Inc. | Combinaisons de composes inhibiteurs d'akt et d'abiraterone et procedes d'utilisation |
EP2714037B1 (fr) | 2011-05-25 | 2016-07-13 | Université Paris Descartes | Inhibiteurs de la voie erk pour le traitement de l'amyotrophie spinale |
WO2013082511A1 (fr) | 2011-12-02 | 2013-06-06 | Genentech, Inc. | Procédés pour surmonter la résistance tumorale aux antagonistes de vegf |
CN103204822B (zh) | 2012-01-17 | 2014-12-03 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的苯并噁唑化合物及其制备方法和用途 |
US20150141470A1 (en) | 2012-05-08 | 2015-05-21 | The Broad Institute, Inc. | Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy |
CN104394855A (zh) | 2012-05-31 | 2015-03-04 | 拜耳医药股份有限公司 | 用于测定肝细胞癌(hcc)患者的治疗的有效响应的生物标记 |
NZ706723A (en) | 2012-10-12 | 2018-07-27 | Exelixis Inc | Novel process for making compounds for use in the treatment of cancer |
HUE055072T2 (hu) | 2013-03-21 | 2021-10-28 | Array Biopharma Inc | B-Raf gátlót és második gátlószert tartalmazó kombinációs terápia |
WO2015038704A1 (fr) | 2013-09-11 | 2015-03-19 | The J. David Gladstone Institutes, A Testamentary Trust Established Under The Will Of J. David Gladstone | Compositions pour prépaprer des cardiomyocytes |
CN105384754B (zh) * | 2014-09-02 | 2018-04-20 | 上海科州药物研发有限公司 | 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途 |
US20190008859A1 (en) | 2015-08-21 | 2019-01-10 | Acerta Pharma B.V. | Therapeutic Combinations of a MEK Inhibitor and a BTK Inhibitor |
AR108257A1 (es) | 2016-05-02 | 2018-08-01 | Mei Pharma Inc | Formas polimórficas de 3-[2-butil-1-(2-dietilamino-etil)-1h-bencimidazol-5-il]-n-hidroxi-acrilamida y usos de las mismas |
US20230192625A1 (en) * | 2017-11-14 | 2023-06-22 | Shenzhen Targetrx, Inc. | Substituted benzimidazole compound and composition comprising same |
KR20210142154A (ko) | 2019-03-21 | 2021-11-24 | 옹쎄오 | 암 치료를 위한 키나제 억제제와 조합된 dbait 분자 |
CA3159348A1 (fr) | 2019-11-08 | 2021-05-14 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Methodes pour le traitement de cancers qui ont acquis une resistance aux inhibiteurs de kinase |
WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
TW202342018A (zh) | 2022-03-04 | 2023-11-01 | 美商奇奈特生物製藥公司 | Mek激酶抑制劑 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5502187A (en) * | 1992-04-03 | 1996-03-26 | The Upjohn Company | Pharmaceutically active bicyclic-heterocyclic amines |
US5525625A (en) * | 1995-01-24 | 1996-06-11 | Warner-Lambert Company | 2-(2-Amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran for treating proliferative disorders |
US6469009B1 (en) * | 1996-04-08 | 2002-10-22 | Ucb, S.A. | Pharmaceutical compositions for the treatment of rhinitis |
US6821963B2 (en) * | 1997-07-01 | 2004-11-23 | Warner-Lambert Company | 4-Bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as MEK inhibitors |
US6506798B1 (en) * | 1997-07-01 | 2003-01-14 | Warner-Lambert Company | 4-Arylamino, 4-aryloxy, and 4-arylthio diarylamines and derivatives thereof as selective MEK inhibitors |
EP1144371B1 (fr) * | 1999-01-13 | 2005-11-09 | Warner-Lambert Company Llc | Derives de benzenesulfonamide et leur utilisation comme inhibiteurs de mek |
JP4621355B2 (ja) * | 1999-01-13 | 2011-01-26 | ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー | ベンゾ複素環およびmek阻害剤としてのその使用 |
HUP0202319A3 (en) * | 1999-07-16 | 2004-12-28 | Warner Lambert Co | Use of mek inhibitors for the preparation of pharmaceutical compositions treating chronic pain |
-
2003
- 2003-03-13 AR ARP030100888A patent/AR038972A1/es not_active Application Discontinuation
- 2003-03-13 WO PCT/US2003/007565 patent/WO2003077855A2/fr active Application Filing
- 2003-03-13 IL IL16399603A patent/IL163996A0/xx unknown
- 2003-03-13 AU AU2003220202A patent/AU2003220202A1/en not_active Abandoned
- 2003-03-13 CN CNA038107678A patent/CN1652792A/zh active Pending
- 2003-03-13 DO DO2003000614A patent/DOP2003000614A/es unknown
- 2003-03-13 CA CA002478534A patent/CA2478534A1/fr not_active Abandoned
- 2003-03-13 PL PL378635A patent/PL378635A1/pl unknown
- 2003-03-13 KR KR10-2004-7014206A patent/KR20040098013A/ko not_active Application Discontinuation
- 2003-03-13 RU RU2004127925/04A patent/RU2300528C2/ru not_active IP Right Cessation
- 2003-03-13 TW TW092105719A patent/TW200406203A/zh unknown
- 2003-03-13 PA PA20038569201A patent/PA8569201A1/es unknown
- 2003-03-13 UA UA20040907721A patent/UA76837C2/uk unknown
- 2003-03-13 US US10/387,682 patent/US20030216460A1/en not_active Abandoned
- 2003-03-13 MX MXPA04008894A patent/MXPA04008894A/es not_active Application Discontinuation
- 2003-03-13 JP JP2003575909A patent/JP2005526076A/ja active Pending
- 2003-03-13 EP EP03716498A patent/EP1482944A4/fr not_active Withdrawn
-
2004
- 2004-09-10 CO CO04090140A patent/CO5611145A2/es not_active Application Discontinuation
-
2005
- 2005-10-25 US US11/258,398 patent/US20060106225A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20060106225A1 (en) | 2006-05-18 |
AU2003220202A1 (en) | 2003-09-29 |
UA76837C2 (uk) | 2006-09-15 |
KR20040098013A (ko) | 2004-11-18 |
TW200406203A (en) | 2004-05-01 |
WO2003077855A2 (fr) | 2003-09-25 |
CO5611145A2 (es) | 2006-02-28 |
EP1482944A4 (fr) | 2006-04-19 |
DOP2003000614A (es) | 2009-09-30 |
CN1652792A (zh) | 2005-08-10 |
CA2478534A1 (fr) | 2003-09-25 |
WO2003077855A3 (fr) | 2004-03-04 |
RU2300528C2 (ru) | 2007-06-10 |
PL378635A1 (pl) | 2006-05-15 |
RU2004127925A (ru) | 2005-05-27 |
JP2005526076A (ja) | 2005-09-02 |
PA8569201A1 (es) | 2004-05-21 |
AR038972A1 (es) | 2005-02-02 |
EP1482944A2 (fr) | 2004-12-08 |
MXPA04008894A (es) | 2005-06-20 |
US20030216460A1 (en) | 2003-11-20 |
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