ABSTRACT
DPC168, a benzylpiperidine-substituted aryl urea CCR3 antagonist evaluated in clinical trials, was a relatively potent inhibitor of the 2D6 isoform of cytochrome P-450 (CYP2D6). Replacement of the cyclohexyl central ring with saturated heterocycles provided potent CCR3 antagonists with improved selectivity against CYP2D6. The favorable preclinical profile of DPC168 was maintained in an acetylpiperidine derivative, BMS-570520.
Subject(s)
Benzyl Compounds/chemistry , Benzyl Compounds/pharmacology , Cytochrome P-450 CYP2D6 Inhibitors , Phenylurea Compounds/chemistry , Piperidines/chemistry , Piperidines/pharmacology , Receptors, Chemokine/antagonists & inhibitors , Animals , Benzyl Compounds/chemical synthesis , Biological Assay , Cells, Cultured , Humans , Mice , Pan troglodytes , Phenylurea Compounds/pharmacology , Piperidines/chemical synthesis , Receptors, CCR3 , Structure-Activity RelationshipABSTRACT
Factor Xa, a serine protease, is at the critical juncture between the intrinsic and extrinsic pathways of the coagulation cascade. Inhibition of factor Xa has the potential to provide effective treatment for both venous and arterial thrombosis. We recently described a series of meta-substituted phenylpyrazoles that are highly potent, selective, and orally bioavailable factor Xa inhibitors. In this paper we report our efforts to further optimize the selectivity profile of our factor Xa inhibitors with a series of ortho- and/or para-substituted phenylpyrazole derivatives. The most potent compounds display sub-nanomolar inhibition constants for factor Xa and show greater than 1000-fold selectivity against other serine proteases. These compounds are also effective in a rabbit model of arteriovenous shunt thrombosis. Optimization of this series led to the preclinical development of DPC602, a 2-(aminomethyl)phenylpyrazole analogue, as a highly potent, selective, and orally bioavailable factor Xa inhibitor.
