Abstract
The design, synthesis and SAR of amido-(propyl and allyl)-hydroxybenzamidine coagulation factor Xa inhibitors is described. These achiral inhibitors are selective for fXa vis a vis structurally related serine proteases and are readily prepared in 6–7 linear steps. The most potent member 9j (fXa Ki=0.75 nM) is selective (>1000-fold) and an effective anticoagulant in mammalian plasma.
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