Design, Synthesis and Biological Evaluation of a Library of Thiocarbazates and Their Activity as Cysteine Protease Inhibitors

Title: Design, Synthesis and Biological Evaluation of a Library of Thiocarbazates and Their Activity as Cysteine Protease Inhibitors

Volume: 13 Issue: 4

Author(s): Zhuqing Liu, Michael C. Myers, Parag P. Shah, Mary Pat Beavers, Phillip A. Benedetti, Scott L. Diamond, Amos B. Smith,III and Donna M. Huryn

Affiliation:

Keywords: Thiocarbazates, cathepsin B, cathepsin S, cathepsin L, cysteine protease inhibitor, library

Abstract: Recently, we identified a novel class of potent cathepsin L inhibitors, characterized by a thiocarbazate warhead. Given the potential of these compounds to inhibit other cysteine proteases, we designed and synthesized a library of thiocarbazates containing diversity elements at three positions. Biological characterization of this library for activity against a panel of proteases indicated a significant preference for members of the papain family of cysteine proteases over serine, metallo-, and certain classes of cysteine proteases, such as caspases. Several potent inhibitors of cathepsin L and S were identified. The SAR data were employed in docking studies in an effort to understand the structural elements required for cathepsin S inhibition. This study provides the basis for the design of highly potent and selective inhibitors of the papain family of cysteine proteases.

Cite this article as:

Liu Zhuqing, C. Myers Michael, P. Shah Parag, Pat Beavers Mary, A. Benedetti Phillip, L. Diamond Scott, B. Smith,III Amos and M. Huryn Donna, Design, Synthesis and Biological Evaluation of a Library of Thiocarbazates and Their Activity as Cysteine Protease Inhibitors, Combinatorial Chemistry & High Throughput Screening 2010; 13 (4) . https://dx.doi.org/10.2174/138620710791054303

DOI https://dx.doi.org/10.2174/138620710791054303	Print ISSN 1386-2073
Publisher Name Bentham Science Publisher	Online ISSN 1875-5402