化学
排泄
肾葡萄糖重吸收
辛烷值
泌尿系统
选择性
药理学
2型糖尿病
糖尿病
内分泌学
生物化学
催化作用
有机化学
医学
作者
Yao Li,Zongjun Shi,Lei Chen,Suxin Zheng,Sheng Li,Bo Xu,Zhenhong Liu,Jianyu Liu,Chongyang Deng,Fei Ye
标识
DOI:10.1021/acs.jmedchem.6b01818
摘要
A new class of potent and highly selective SGLT2 inhibitors is disclosed. Compound 31 (HSK0935) demonstrated excellent hSGLT2 inhibition of 1.3 nM and a high hSGLT1/hSGLT2 selectivity of 843-fold. It showed robust urinary glucose excretion in Sprague-Dawley (SD) rats and affected more urinary glucose excretion in Rhesus monkeys. Finally, an efficient synthetic route has been developed featuring a ring-closing cascade reaction to incorporate a double ketal 1-methoxy-6,8-dioxabicyclo[3.2.1]octane ring system.
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