79612-79-6Relevant articles and documents
SYNTHESIS AND PROPERTIES OF AMIDES OF 2-SUBSTITUTED 3-ARYL- AND 3-PYRIDYLAMINOACRYLIC ACIDS
Mikhalev, A. I.,Ukhov, S. V.,Konshin, M. E.
, p. 551 - 555 (1994)
The reaction of aryl- or pyridylamines with ethyl orthoformate and malonanilic acid gave amides of 2-(N-arylcarbamoyl)-, 2-cyano-, 2-ethoxycarbonyl-3-aryloaminoacrylic acids and their corresponding 3-pyridyl analogs.IR and PMR spectroscopy indicates that
HCV NS3 PROTEASE INHIBITORS
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Page/Page column 63; 64, (2013/06/05)
The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.
SIX-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS
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Page/Page column 101, (2008/06/13)
The present invention provides compounds of Formula (I), or a stereoisomer, tautomer, pharmaceutically acceptable salt or solvate form thereof, wherein the variables A, B, R3 and R11 are as defined herein. The compounds of Formula (I) are useful as selective inhibitors of serine protease enzymes of the coagulation cascade and/or contact activation system; for example thrombin, factor Xa, factor XIa, factor IXa, factor VIIa and/or plasma kallikrein. In particular, it relates to compounds that are selective factor XIa inhibitors or dual inhibitors of fXIa and plasma kallikrein. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating thromboembolic and/or inflammatory disorders using the same.