HDAC8 as an emerging target in drug discovery with special emphasis on medicinal chemistry

被引:6
|
作者
Rajaraman, Srinidhi [1 ]
Balakrishnan, Ranjani [1 ]
Deshmukh, Dhruv [1 ]
Ganorkar, Abhiram [1 ]
Biswas, Swati [1 ]
Pulya, Sravani [1 ]
Ghosh, Balaram [1 ]
机构
[1] Birla Inst Technol & Sci Pilani, Dept Pharm, Epigenet Res Lab, Hyderabad Campus, Hyderabad 500078, India
关键词
cancer; epigenetic modulator; HDAC8 selective inhibitor; histone deacetylase 8; structure-activity relationship; HISTONE DEACETYLASE 8; ZINC-BINDING GROUPS; BIOLOGICAL EVALUATION; BENZAMIDE CLASS; INHIBITORS; DESIGN; ACETYLATION; CANCER; CLONING; CELLS;
D O I
10.4155/fmc-2023-0054
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
HDAC8 catalyzes the deacetylation of both histones and nonhistone proteins. The abnormal expression of HDAC8 is associated with various pathological conditions causing cancer and other diseases like myopathies, Cornelia de Lange syndrome, renal fibrosis, and viral and parasitic infections. The substrates of HDAC8 are involved in diverse molecular mechanisms of cancer such as cell proliferation, invasion, metastasis and drug resistance. Based on the crystal structures and the key residues at the active site, HDAC8 inhibitors have been designed along the canonical pharmacophore. This article details the importance, recent advancements, and the structural and functional aspects of HDAC8 with special emphasis on the medicinal chemistry aspect of HDAC8 inhibitors that will help in developing novel epigenetic therapeutics.
引用
收藏
页码:885 / 908
页数:24
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