葛根素
葡萄糖苷
化学
胰岛素抵抗
糖尿病
2型糖尿病
体外
胰岛素
脂肪细胞
药理学
生物活性
化学合成
内科学
内分泌学
生物化学
医学
脂肪组织
病理
替代医学
作者
Eisuke Kato,Jun Kawabata
标识
DOI:10.1016/j.bmcl.2010.06.077
摘要
Chemical treatment of diabetes mellitus is widely studied and controlling of blood glucose level is the main course of therapy. In type 2 diabetes mellitus, insulin resistance is the major problem. An isoflavone C-glucoside, puerarin (1), is known to enhance glucose uptake into the insulin sensitive cell and is thought to be a candidate for treatment of diabetes mellitus. We synthesized 1 and several derivatives to apply for the structure-activity relationship study. The result against 3T3-L1 adipocyte indicated that the C-glucoside part of 1 is unconcerned in its activity when tested in vitro and the main structure responsible for its activity was the isoflavone moiety.
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