发明名称 Glucopyranosyloxypyrazole derivatives and use thereof in medicines
摘要 The present invention provides glucopyranosyloxypyrazole derivative of the formula (I) wherein R represents a hydrogen atom, alkyl group having 1 to 6 carbon atoms, acyl group having 2 to 7 carbon atoms, alkoxycarbonyl group having 2 to 7 carbon atoms, hydroxymethyl O substituted with acyl group having 2 to 7 carbon atoms, or O substituted with alkoxycarbonyl group having 2 to 7 carbon atoms, one of Q and T represents a group represented by the formula (A), wherein P represents a hydrogen atom, acyl group having 2 to 7 carbon atoms substituted with alkoxy group having 1 to 6 carbon atoms, with alkoxycarbonyl group having 2 to 7 carbon atoms, alkoxycarbonyl group having 2 to 7 carbon atoms substituted with alkoxy group having 1 to 6 carbon atoms; and second is alkyl group having 1 to 6 carbon atoms, eventually substituted with 1 to 3 halogen atoms; R2 represents a hydrogen atom, alkyl group having 1 to 6 carbon atoms, optionally substituted with 1 to 3 halogen atoms, alkoxy group having 1 to 6 carbon atoms, alkylthio group having 1 to 6 carbon atoms or a halogen; or pharmaceutically acceptable salts thereof. A pharmaceutical composition comprising this derivative. Said derivative or pharmaceutical composition for the use as a human SGL T2 inhibitor, an agent for the prevention or treatment of a disease associated with hyperglycemia such as diabetes and obesity. A pharmaceutical combinations comprising this derivative.
申请公布号 SK287786(B6) 申请公布日期 2011.09.05
申请号 SK20030000809 申请日期 2001.12.25
申请人 KISSEI PHARMACEUTICAL CO., LTD. 发明人 FUJIKURA HIDEKI;FUSHIMI NOBUHIKO;NISHIMURA TOSHIHIRO;NAKABAYASHI TAKESHI;ISAJI MASAYUKI
分类号 C07H17/02;A61K31/7056;A61P3/04;A61P3/06;A61P3/10;A61P7/10;A61P9/04;A61P9/10;A61P9/12;A61P19/06;A61P43/00 主分类号 C07H17/02
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