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Glycosylated dihydrochalcones as potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitors.

作者信息

Dudash Joseph, Zhang Xiaoyan, Zeck Roxanne E, Johnson Sigmond G, Cox Geoffrey G, Conway Bruce R, Rybczynski Philip J, Demarest Keith T

机构信息

Johnson & Johnson Pharmaceutical Research and Development, L.L.C., 1000 Rt. 202, PO Box 300, Raritan, NJ 08869, USA.

出版信息

Bioorg Med Chem Lett. 2004 Oct 18;14(20):5121-5. doi: 10.1016/j.bmcl.2004.07.082.

DOI:10.1016/j.bmcl.2004.07.082
PMID:15380212
Abstract

A series of glucose conjugates was synthesized and tested for inhibition of SGLT1 and SGLT2. The core structure was derived from compound 1a. Modification of the benzofuran moiety and 4'-substituent of the phenyl ring in compound 1a improved selectivity at SGLT2. Select compounds were compared to 1a in metabolic stability and in vivo efficacy studies.

摘要

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