2014年8月21日木曜日

Benzisothiazole- and Indolizine-β-d-glucopyranoside Inhibitors of SGLT2



Abstract

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A series of benzisothiazole- and indolizine-β-d-glucopyranoside inhibitors of human SGLT2 are described. The synthesis of the C-linked heterocyclic glucosides took advantage of a palladium-catalyzed cross-coupling reaction between a glucal boronate and the corresponding bromo heterocycle. The compounds have been evaluated for their human SGLT2 inhibition potential using cell-based functional transporter assays, and their structure−activity relationships have been described. Benzisothiazole-C-glucoside 16d was found to be an inhibitor of SGLT2 with an IC50 of 10 nM.

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  1. Isomangiferin, a natural product, has antiviral effect due to their capability of inhibiting virus replication within cells. Isomangiferin

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