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Design, synthesis, and in vitro biological activity of benzimidazole based factor Xa inhibitors.

Bioorganic & medicinal chemistry letters (2000-06-15)
Z Zhao, D O Arnaiz, B Griedel, S Sakata, J L Dallas, M Whitlow, L Trinh, J Post, A Liang, M M Morrissey, K J Shaw
ABSTRACT

Inhibitors based on the benzimidazole scaffold showed subnanomolar potency against Factor Xa with 500-1000-fold selectivity against thrombin and 50-100-fold selectivity against trypsin. The 2-substituent on the benzimidazole ring had a strong impact on the FXa inhibitory activity. Crystallography studies suggest that the 2-substituent may have a conformational effect favoring the extended binding conformation.

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Sigma-Aldrich
4-Amino-3-nitrophenol, 98%