NAD+激酶
疾病
药理学
药物发现
计算生物学
医学
生物信息学
生物
生物化学
酶
内科学
作者
Ziyan Zhou,Tianfang Ma,Qihua Zhu,Yungen Xu,Xiaoming Zha
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2018-04-01
卷期号:10 (8): 907-934
被引量:29
标识
DOI:10.4155/fmc-2017-0207
摘要
Sirtuins (SIRT) are coenzyme NAD+-dependent histone deacetylases for the transfer of modified acetyl groups. Sirtuins are widely involved in various physiological processes and therefore associated with cardiovascular disease, diabetes, Parkinson's disease, cancer and beyond. Consequently, the development of modulators for sirtuins has considerable clinical value. To date, a variety of SIRT1/2 inhibitors have been reported and none has been approved for the market. This review summarizes the recent progress in the discovery and development of SIRT1/2 inhibitors including their inhibitory potency, structure-activity relationship and binding mode analysis as well as discusses the perspective for the future development of SIRT1/2 inhibitors.
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