Author/Authors :
Michael S. South، نويسنده , , Thomas A. Dice، نويسنده , , Thomas J. Girard، نويسنده , , Rhonda M. Lachance، نويسنده , , Anna M. Stevens، نويسنده , , Roderick A. Stegeman، نويسنده , , William C. Stallings، نويسنده , , Ravi G. Kurumbail، نويسنده , , John J. Parlow، نويسنده ,
Abstract :
A solution-phase synthesis of an α-ketothiazole library of the general form -Phe- -AA- -Arg-α-ketothiazole is described. The five-step synthesis is accomplished using a combination of polymeric reagents and polymer-assisted solution-phase purification protocols, including reactant-sequestering resins, reagent-sequestering resins, and tagged reagents. The multi-step synthesis affords the desired α-ketothiazole products in excellent purities and yields. A variety of -amino acid inputs were used to probe the S2 pocket of the tissue factor (TF) VIIa enzyme to influence both potency and selectivity. An X-ray crystal structure of compound 10e bound to the TF/VIIa complex was obtained that explains the observed selectivity. The α-ketothiazoles were found to be potent, reversible-covalent inhibitors of tissue factor VIIa, with some analogues demonstrating selectivity versus thrombin.