SIRT2
锡尔图因
化学
酰化
乙酰化
小分子
共价键
药理学
生物化学
立体化学
基因
生物
催化作用
有机化学
作者
Xiaoxue Chen,Yefang Zou,Jie Wang,Zhengxuan Cao,Jingzi Liu,Li Yan,Yong‐Long Zhao,Bin He
标识
DOI:10.1016/j.bmc.2020.115353
摘要
A series of sirtuin inhibitor candidates were assembled based on an intermediate ester (1a) our accidently discovered. After screening and evaluation, several SIRT2 selective inhibitors were identified, which can inhibit all the deacetylation, defatty-acylation and debenzoylation of SIRT2. Among these inhibitors, compound 1e was the best SIRT2 selective inhibitors. The primary study on the inhibitory mechanism indicated that compound 1e may be a suicide inhibitor acting as an irreversible way. Given almost all reported sirtuin inhibitors are non-covalent, sirtuin covalent inhibitors are still need to be developed. These findings will facilitate for further development of SIRT2 selective and suicide inhibitors.
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