Structure-based design, synthesis and evaluation of conformationally constrained cysteine protease inhibitors

Abstract

The inhibition of cysteine proteases is being studied as a strategy to combat parasitic diseases such as Chagas' disease, leishmaniasis, and malaria. Cruzain is the major cysteine protease of Trypanosoma cruzi, the etiologic agent of Chagas' disease. A crystal structure of cruzain, covalently inactivated by fluoromethyl ketone inhibitor 1 (Cbz-Phe-Ala-FMK), was used as a template to design potential inhibitors. Conformationally constrained γ-lactams containing electrophilic aldehyde ( 12, 17, 18, 25, 26, and 29) or vinyl sulfone ( 43, 44, and 46) units were synthesized. Constrained lactam 26 had IC 50 values of ca. 20 nM against the Leishmania major protease and ca. 50 nM versus falcipain, an important cysteine protease isolated from Plasmodium falciparum. However, all of the conformationally constrained inhibitors were weak inhibitors of cruzain, compared to unconstrained peptide aldehyde (e.g. 5) and vinyl sulfone inhibitors (e.g. 48, which proved to be an excellent inhibitor of cruzain with an apparent second order inhibition rate constant ( k inact/ K i) of 634,000 s −1M −1). A significant reduction in activity was also observed with acyclic inhibitors 30 and 51 containing α-methyl phenylalanine residues at the P 2 position. These data indicate that the pyrrolidinone ring, especially the quarternary center at P 2, interferes with the normal substrate binding mode with cruzain, but not with falcipain or the leishmania protease.