Benzimidazolone as potent chymase inhibitor: Modulation of reactive metabolite formation in the hydrophobic (P1) region
摘要:
A new class of chymase inhibitor featuring a benzimidazolone core with an acid side chain and a P-1 hydrophobic moiety is described. Incubation of the lead compound with GSH resulted in the formation of a GSH conjugate on the benzothiophene P-1 moiety. Replacement of the benzothiophene with different heterocyclic systems such as indoles and benzoisothiazole is feasible. Among the P-1 replacements, benzoisothiazole prevents the formation of GSH conjugate and an in silico analysis of oxidative potentials agreed with the experimental outcome. (C) 2011 Elsevier Ltd. All rights reserved.
Disclosed are small molecule inhibitors which are useful in treating various diseases and conditions involving chymase.
公开了一种小分子抑制剂,其在治疗涉及chymase的各种疾病和病况方面是有用的。
WO2008/147697
申请人:——
公开号:——
公开(公告)日:——
BENZIMIDAZOLONE CHYMASE INHIBITORS
申请人:Boehringer Ingelheim International GmbH
公开号:EP2152674B1
公开(公告)日:2011-08-03
US9150556B2
申请人:——
公开号:US9150556B2
公开(公告)日:2015-10-06
[EN] BENZIMIDAZOLONE CHYMASE INHIBITORS<br/>[FR] INHIBITEURS DE BENZIMIDAZOLONE CHYMASE
申请人:BOEHRINGER INGELHEIM INT
公开号:WO2008147697A1
公开(公告)日:2008-12-04
[EN] Disclosed are small molecule inhibitors which are useful in treating various diseases and conditions involving chymase. [FR] L'invention concerne des inhibiteurs à petites molécules qui sont utiles dans le traitement de diverses maladies et affections impliquant la chymase.