The present application describes imidazo-heterobicycles of formulas I and III:
1
or pharmaceutically acceptable salt or prodrug forms thereof. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.
本申请描述了I和III公式的
咪唑杂环:1或其药学上可接受的盐或前药形式。本发明的化合物可用作胰
蛋白酶样
丝氨酸蛋白酶的
抑制剂,具体地是Xa因子的
抑制剂。