5- AND 6- SUBSTITUTED BENZIMIDAZOLE THIOPHENE COMPOUNDS
申请人:Rheault Tara Renae
公开号:US20100056525A1
公开(公告)日:2010-03-04
The present invention provides 5- and 6-substituted benzimidazole thiophene compounds pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents.
5- AND 6-SUBSTITUTED BENZIMIDAZOLE THIOPHENE COMPOUNDS
申请人:SmithKline Beecham Corporation
公开号:EP2079733A2
公开(公告)日:2009-07-22
[EN] 5- AND 6- SUBSTITUTED BENZIMIDAZOLE THIOPHENE COMPOUNDS<br/>[FR] BENZIDIMIDAZOLE THIOPHÈNES SUBSTITUÉS EN 5 ET 6 POUR PLK
申请人:SMITHKLINE BEECHAM CORP
公开号:WO2008070354A2
公开(公告)日:2008-06-12
[EN] The present invention provides 5- and 6-substituted benzimidazole thiophene compounds pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents. [FR] La présente invention concerne des composés benzimidazole thiophène substitués en 5 et 6 et des compositions pharmaceutiques les contenant, des procédés pour les préparer et leur utilisation en tant qu'agents pharmaceutiques.
Heteroaryl-linked 5-(1H-benzimidazol-1-yl)-2-thiophenecarboxamides: Potent inhibitors of polo-like kinase 1 (PLK1) with improved drug-like properties
作者:Tara R. Rheault、Kelly H. Donaldson、Jennifer G. Badiang-Alberti、Ronda G. Davis-Ward、C. Webb Andrews、Ramesh Bambal、Jeffrey R. Jackson、Mui Cheung
DOI:10.1016/j.bmcl.2010.06.009
日期:2010.8
Potent inhibitors of PLK1 with acceptable solubility, mouse iv clearance, and reduced CYP450 inhibition were identified. Drug-like properties were improved using a heteroaryl ring as a functional handle for manipulation of inhibitors' physiochemical and DMPK properties. (C) 2010 Elsevier Ltd. All rights reserved.