Synthesis of sulfaphenazole derivatives and their use as inhibitors and tools for comparing the active sites of human liver cytochromes P450 of the 2C subfamily

…, S Dijols, C Marques-Soares, C Minoletti…

Index: Ha-Duong; Dijols; Marques-Soares; Minoletti; Dansette; Mansuy Journal of Medicinal Chemistry, 2001 , vol. 44, # 22 p. 3622 - 3631

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Citation Number: 33

Abstract

Twenty-three new derivatives of sulfaphenazole (SPA) were synthesized to further explore the topology of the active sites of human liver cytochromes P450 of the 2C subfamily and to find new selective inhibitors of these cytochromes. These compounds are derived from SPA by replacement of the NH2 and H (of the SO2NH function) substituents of SPA with various R1 and R2 groups, respectively. Their inhibitory effects were studied on recombinant CYP ...