表观遗传学
背景(考古学)
酰肼
药品
计算生物学
药物发现
组蛋白脱乙酰基酶
疾病
药理学
化学
生物信息学
组蛋白
生物
医学
生物化学
基因
内科学
古生物学
有机化学
作者
Suvankar Banerjee,Sandip Kumar Baidya,Nilanjan Adhikari,Tarun Jha,Balaram Ghosh
标识
DOI:10.2174/1568026623666230405124207
摘要
Abstract: Epigenetic modulations by HDACs are associated with multiple disease conditions. In this context, HDACs play vital roles in the progression of diseases including several cancers, neu-rodegenerative diseases, inflammatory diseases, and metabolic disorders. Though several HDAC inhibitors have been established as drug candidates, their usage has been restricted because of broad-spectrum inhibition, highly toxic character, and off-target adverse effects. Therefore, specific HDAC selectivity is essential to get rid of such adverse effects. Hydrazide-based compounds have already been proven to exert higher inhibitory efficacy and specific HDAC selectivity. In this arti-cle, the detailed structure-activity relationship (SAR) of the existing hydrazide-based HDAC inhibi-tors has been elucidated to gather crucial information that can be utilized further for the develop-ment of promising drug candidates for combating diverse diseases in the future.
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