Heteroaryl-O-glucosides as novel sodium glucose co-transporter 2 inhibitors. Part 1
摘要:
A series of benzo-fused heteroaryl-O-glucosides was synthesized and evaluated in SGLT1 and 2 cell-based functional assays. Indole-O-glucoside 10a and benzimidazole-O-glucoside 18 exhibited potent in vitro SGLT2 inhibitory activity. (c) 2005 Elsevier Ltd. All rights reserved.
Heteroaryl-O-glucosides as novel sodium glucose co-transporter 2 inhibitors. Part 1
摘要:
A series of benzo-fused heteroaryl-O-glucosides was synthesized and evaluated in SGLT1 and 2 cell-based functional assays. Indole-O-glucoside 10a and benzimidazole-O-glucoside 18 exhibited potent in vitro SGLT2 inhibitory activity. (c) 2005 Elsevier Ltd. All rights reserved.
Substituted benzimidazole-, benztriazole-, and benzimidazolone-O-glucosides
申请人:Urbanski Maud
公开号:US20050032712A1
公开(公告)日:2005-02-10
This invention relates to to substituted benzimidazole-O-glucosides, benztriazole-O-glucosides, and benzimidazolone-O-glucosides, compositions containing them, and methods of using them, for example, for the treatment or prophylaxis of diabetes and Syndrome X.
本发明涉及取代的苯并咪唑-O-葡萄糖苷、苯并三唑-O-葡萄糖苷和苯并咪唑酮-O-葡萄糖苷、含有它们的组合物以及使用它们的方法,例如用于治疗或预防糖尿病和 X 综合征。
SUBSTITUTED BENZIMIDAZOLE-, BENZTRIAZOLE-, AND BENZIMIDAZOLONE-O-GLUCOSIDES