2-Aryl benzimidazoles featuring alkyl-linked pendant alcohols and amines as inhibitors of checkpoint kinase Chk2
摘要:
A series of benzimidazole compounds containing pendant alcohol and amine moieties was found to be active against checkpoint kinase Chk2. These compounds were prepared to examine a potential hydrogen bond interaction with an active site residue and to investigate replacement of a biaryl linker with an aliphatic system in an effort to improve solubility. (c) 2007 Elsevier Ltd. All rights reserved.
ARYL-SUBSTITUTED BENZIMIDAZOLE AND IMIDAZOPYRIDINE ETHERS AS ANTI-CANCER AGENTS
申请人:JANSSEN PHARMACEUTICA N.V.
公开号:EP1824832A1
公开(公告)日:2007-08-29
US7250427B2
申请人:——
公开号:US7250427B2
公开(公告)日:2007-07-31
[EN] ARYL-SUBSTITUTED BENZIMIDAZOLE AND IMIDAZOPYRIDINE ETHERS AS ANTI-CANCER AGENTS<br/>[FR] ETHERS BENZIMIDAZOLE A SUBSTITUTION ARYLE ET IMIDAZOPYRIDINE, COMME ANTICANCEREUX
申请人:JANSSEN PHARMACEUTICA NV
公开号:WO2006004791A1
公开(公告)日:2006-01-12
Aryl substituted benzimidazole and imidazo[4,5]Aryl substituted benzimidazole and imidazo[4,5]Aryl substituted benzimidazole and imidazo[4,5]pyridine ethers are described as inhibitors of Cds1 and useful as adjuvants to chemotherapy or radiation therapy in the treatment of cancer.