Synthesis, evaluation and molecular modelling of piceatannol analogues as arginase inhibitors - Archive ouverte HAL
Article Dans Une Revue RSC Medicinal Chemistry Année : 2020

Synthesis, evaluation and molecular modelling of piceatannol analogues as arginase inhibitors

Résumé

Arginase is involved in a wide range of pathologies including cardiovascular diseases and infectious diseases whilst it is also a promising target to improve cancer immunotherapy. To date, only a limited number of inhibitors of arginase have been reported. Natural polyphenols, among them piceatannol, are moderate inhibitors of arginase. Herein, we report our efforts to investigate catechol binding by quantum chemistry and generate analogues of piceatannol. In this work, we synthesized a novel series of amino-polyphenols which were then evaluated as arginase inhibitors. Their structure–activity relationships were elucidated by deep quantum chemistry modelling. 4-((3,4-Dihydroxybenzyl)amino)benzene-1,2-diol 3t displays a mixed inhibition activity on bovine and human arginase I with IC50 (Ki) values of 76 (82) μM and 89 μM, respectively.

Domaines

Chimie organique

Dates et versions

hal-02900460 , version 1 (16-07-2020)

Identifiants

Citer

J. Muller, B. Cardey, A. Zedet, C. Desingle, M. Grzybowski, et al.. Synthesis, evaluation and molecular modelling of piceatannol analogues as arginase inhibitors. RSC Medicinal Chemistry, 2020, 11 (5), pp.559-568. ⟨10.1039/D0MD00011F⟩. ⟨hal-02900460⟩
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