The present application describes 5-6 or 5-7 heterobicyclics of Formula I:
1
or pharmaceutically acceptable salt forms thereof, wherein ring P is a 5-membered heteroaromatic and ring M is a 6 or 7-membered non-aromatic 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:1的5-6或5-7
杂环化合物,或其药学上可接受的盐形式,其中环P是5-成员的杂芳族环,环M是6或7-成员的非芳族碳环或杂环。本发明化合物可用作凝血酶样
丝氨酸蛋白酶的
抑制剂,特别是Xa因子的
抑制剂。