Design, synthesis, and structure-activity relationships of a series of 4-benzyl-5-isopropyl-1H-pyrazol-3-yl β-D-glycopyranosides substituted with novel hydrophilic groups as highly potent inhibitors of sodium glucose co-transporter 1 (SGLT1).

Citation: Fushimi N, Teranishi H, Shimizu K, Yonekubo S, Ohno K, Miyagi T, Itoh F, Shibazaki T, Tomae M, Ishikawa-Takemura Y, Nakabayashi T, Kamada N, Yamauchi Y, Kobayashi S, Isaji M.: Design, synthesis, and structure-activity relationships of a series of 4-benzyl-5-isopropyl-1H-pyrazol-3-yl β-D-glycopyranosides substituted with novel hydrophilic groups as highly potent inhibitors of sodium glucose co-transporter 1 (SGLT1). Bioorg Med Chem, Volume 21 (3), 2013
Authors: Fushimi N, Miyagi T, Ohno K, Shimizu K, Teranishi H, Yonekubo S, Isaji M., Ishikawa-Takemura Y, Itoh F, Kamada N, Kobayashi S, Nakabayashi T, Shibazaki T, Tomae M, Yamauchi Y
Journal: Bioorg Med Chem
Year: 2013
DOI: 10.1016/j.bmc.2012.11.041
PubMed: 23273606
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