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Synthesis and antiviral evaluation of novel peptidomimetics as norovirus protease inhibitors.

ABSTRACT: A series of tripeptidyl transition state inhibitors with new P1 and warhead moieties were synthesized and evaluated in a GI-1 norovirus replicon system and against GII-4 and GI-1 norovirus proteases. Compound 19, containing a 6-membered ring at the P1 position and a reactive aldehyde warhead exhibited sub-micromolar replicon inhibition. Retaining the same peptidyl scaffold, several reactive warheads were tested for protease inhibition and norovirus replicon inhibition. Of the six that were synthesized and tested, compounds 42, 43, and 45 potently inhibited the protease in biochemical assay and GI-1 norovirus replicon in the nanomolar range.

SUBMITTER: Amblard F

PROVIDER: S-EPMC6425952 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

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Synthesis and antiviral evaluation of novel peptidomimetics as norovirus protease inhibitors.

Amblard Franck F Zhou Shaoman S Liu Peng P Yoon Jack J Cox Bryan B Muzzarelli Kendall K Kuiper Benjamin D BD Kovari Ladislau C LC Schinazi Raymond F RF

Bioorganic & medicinal chemistry letters 20180508 12

A series of tripeptidyl transition state inhibitors with new P1 and warhead moieties were synthesized and evaluated in a GI-1 norovirus replicon system and against GII-4 and GI-1 norovirus proteases. Compound 19, containing a 6-membered ring at the P1 position and a reactive aldehyde warhead exhibited sub-micromolar replicon inhibition. Retaining the same peptidyl scaffold, several reactive warheads were tested for protease inhibition and norovirus replicon inhibition. Of the six that were synth ...[more]

PMID: 29779977

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