6-5, 6-6, or 6-7 Heterobicycles as factor xa inhibitors

摘要

The present application describes 6-5, 6-6, or 6-7 heterobicycles of Formula I or pharmaceutically acceptable salt forms thereof: wherein ring P is a 6-membered heteroaromatic and ring M is a 5-, 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.