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Bioorg Med Chem Lett ; 12(12): 1671-4, 2002 Jun 17.
Article in English | MEDLINE | ID: mdl-12039587

ABSTRACT

Further optimization of the beta-aminoester class of factor Xa (fXa) inhibitors is described culminating in the identification of 9c (FXV673), a potent and selective factor Xa inhibitor with excellent in vivo anticoagulant activity. An X-ray structure of FXV673 bound to human fXa is also presented. Based on its selectivity, potent in vivo activity and favorable pre-clinical safety profile, FXV673 was selected for further development and is currently undergoing clinical trials.


Subject(s)
Anticoagulants/chemistry , Anticoagulants/pharmacology , Cyclic N-Oxides/chemistry , Cyclic N-Oxides/pharmacology , Factor Xa Inhibitors , Pyridines/chemistry , Pyridines/pharmacology , Serine Proteinase Inhibitors/chemistry , Serine Proteinase Inhibitors/pharmacology , Crystallography, X-Ray , Esters , Humans , Models, Molecular , Molecular Structure
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