HDAC6型
组蛋白脱乙酰基酶
药效团
药物发现
计算生物学
专家意见
医学
虚拟筛选
药理学
生物信息学
生物
组蛋白
生物化学
基因
重症监护医学
作者
Sida Shen,Alan P. Kozikowski
标识
DOI:10.1080/13543776.2019.1708901
摘要
: Histone deacetylase 6 (HDAC6) is unique in comparison with other zinc-dependent HDAC family members. An increasing amount of evidence from clinical and preclinical research demonstrates the potential of HDAC6 inhibition as an effective therapeutic approach for the treatment of cancer, autoimmune diseases, as well as neurological disorders. The recently disclosed crystal structures of HDAC6-ligand complexes offer further means for achieving pharmacophore refinement, thus further accelerating the pace of HDAC6 inhibitor discovery in the last few years.
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