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Chem Biodivers ; 19(10): e202200562, 2022 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-35965252

RESUMO

Leaves of Combretum quadrangulare Kurz showed potent α-glucosidase inhibition. Two new cycloartane-type triterpenes, combretic acids D and E were isolated from the bioactive fraction. The chemical structures were determined using NMR and MS methods. Combretic acid D represents for the first cycloartane having a dihydrofuran ring in the side chain. Combretic acids D and E showed significant α-glucosidase inhibition, with IC50 values of 13.9 and 30.7 µM, respectively. Combretic acid D was determined to be a non-competitive type in the kinetic study. The docking study in combination with dynamic simulations of this compound provided the molecular understanding of α-glucosidase inhibition.


Assuntos
Combretum , Triterpenos , Humanos , Combretum/química , alfa-Glucosidases , Estrutura Molecular , Triterpenos/química , Povo Asiático , Simulação de Acoplamento Molecular , Inibidores de Glicosídeo Hidrolases/farmacologia
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