Structure–activity relationships of anthranilamide-based factor Xa inhibitors containing piperidinone and pyridinone P4 moieties
摘要:
Introduction of the phenyl piperidinone and phenyl pyridinone P4 moieties in the anthranilamide scaffold led to potent, selective, and orally bioavailable inhibitors of factor Xa. Anthranilamide 28 displayed comparable efficacy to apixaban in the rabbit arteriovenous-shunt (AV) thrombosis model. (c) 2008 Elsevier Ltd. All rights reserved.
LACTAM-CONTAINING COMPOUNDS AND DERIVATIVES THEREOF AS FACTOR XA INHIBITORS
申请人:Bristol-Myers Squibb Company
公开号:US20170050964A1
公开(公告)日:2017-02-23
The present application describes lactam-containing compounds and derivatives thereof of Formula I:
P
4
—P-M-M
4
I
or pharmaceutically acceptable salt forms thereof, wherein ring P, if present is a 5-7 membered carbocycle or heterocycle and ring M is a 5-7 membered carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.
Lactam-containing compounds and derivatives thereof as factor xa inhibitors
申请人:Pinto J.P. Donald
公开号:US20050267097A1
公开(公告)日:2005-12-01
The present application describes lactam-containing compounds and derivatives thereof of Formula I:
P
4
—P-M-M
4
I
or pharmaceutically acceptable salt forms thereof, wherein ring P, if present is a 5-7 membered carbocycle or heterocycle and ring M is a 5-7 membered carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.
Lactam-containing compounds and derivatives thereof as factor XA inhibitors
申请人:Bristol-Myers Squibb Company
公开号:EP2105436A1
公开(公告)日:2009-09-30
The present application describes lactam-containing compounds and derivatives thereof of Formula I: P4-P-M-M-4 or pharmaceutically acceptable salt forms thereof, wherein ring P, if present is a 5-7 membered carbocycle or heterocycle and ring M is a 5-7 membered carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.
本申请描述了式 I 的含内酰胺化合物及其衍生物:P4-P-M-M-4或其药学上可接受的盐形式,其中环P(如果存在)是5-7个成员的碳环或杂环,环M是5-7个成员的碳环或杂环。本发明的化合物可用作胰蛋白酶样丝氨酸蛋白酶,特别是 Xa 因子的抑制剂。