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Pharmacophore model of the quercetin binding site of the SIRT6 protein

…, D Donnelly, M Migliore, P Johnson, C Fishwick…

文献索引:Ravichandran; Singh; Donnelly; Migliore; Johnson; Fishwick; Luke; Martin; Maudsley; Fugmann; Moaddel Journal of Molecular Graphics and Modelling, 2014 , vol. 49, p. 38 - 46

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被引用次数: 11

摘要

Abstract SIRT6 is a histone deacetylase that has been proposed as a potential therapeutic target for metabolic disorders and the prevention of age-associated diseases. We have previously reported on the identification of quercetin and vitexin as SIRT6 inhibitors, and studied structurally related flavonoids including luteolin, kaempferol, apigenin and naringenin. It was determined that the SIRT6 protein remained active after immobilization ...