姜黄素
化学
抑制性突触后电位
体外
酶
对接(动物)
淀粉酶
生物化学
立体化学
内分泌学
生物
医学
护理部
作者
Govindharasu Banuppriya,Rajendran Sribalan,Sulthan Alavudeen Rizwan Fathima,Vediappen Padmini
标识
DOI:10.1002/cbdv.201800105
摘要
Two different series of novel β-ketoamide curcumin analogs enriched in biological activities have been synthesized. The synthesized compounds were screened for their in vitro anti-diabetic and AGEs inhibitory activities and exhibited potent to good anti-diabetic and AGEs inhibitory activities. The molecular docking study was also performed with the α-amylase enzyme.
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