Heterocyclic compounds as inhibitors of factor VIIa

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C514S311000, C514S314000, C514S352000, C514S381000, C514S383000, C514S394000, C514S397000, C514S406000, C546S139000, C546S148000, C546S152000, C546S268100, C546S304000, C548S254000, C548S262200, C548S302700, C548S335100

Reexamination Certificate

active

07576098

ABSTRACT:
The present invention relates generally to compounds that inhibit serine proteases. In particular it is directed to novel heterocyclic compounds, or a stereoisomer or pharmaceutically acceptable salt, solvate, or prodrug form thereof, which are useful as selective inhibitors of serine protease enzymes of the coagulation cascade; for example thrombin, factor VIIa, factor Xa, factor XIa, factor IXa, and/or plasma kallikrein. In particular, it relates to compounds that are factor VIIa inhibitors. This invention also relates to pharmaceutical compositions comprising these compounds and methods of using the same.

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