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Chem Pharm Bull (Tokyo) ; 57(9): 1004-7, 2009 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-19721266

RESUMEN

Based upon the biphenyl 1-(2-naphthyl)-1H-pyrazole-5-carboxylamides reported in our previous communications, we designed and discovered 2-(6-chloro-3-methylsulfonyl)-naphthyl as an optimal factor Xa S1 binding element. Employing a key Diels-Alder reaction of 1,4-dihydro-2,3-benzoxathiin-3-oxide with maleic anhydride and a key Cu(I)-mediated methylsulfonylation, we prepared two biphenyl 1-(2-(6-chloro-3-methylsulfonyl)-naphthyl)-1H-pyrazole-5-carboxylamides as highly potent factor Xa inhibitors with K(i) values of 0.065 nM and 0.045 nM respectively, and demonstrated the synergistically enhanced binding interaction in the factor Xa S1 site.


Asunto(s)
Amidas/síntesis química , Inhibidores del Factor Xa , Inhibidores de Serina Proteinasa/síntesis química , Amidas/química , Amidas/farmacología , Sitios de Unión , Diseño de Fármacos , Factor Xa/metabolismo , Unión Proteica , Inhibidores de Serina Proteinasa/química , Inhibidores de Serina Proteinasa/farmacología
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