LIU Ren-shuai, FANG Hao. Histone deacetylase 6: structure, functions and development of selective inhibitorsJ. Acta Pharmaceutica Sinica, 2015,50(1): 7-14.
Citation: LIU Ren-shuai, FANG Hao. Histone deacetylase 6: structure, functions and development of selective inhibitorsJ. Acta Pharmaceutica Sinica, 2015,50(1): 7-14.

Histone deacetylase 6: structure, functions and development of selective inhibitors

  • Histone deacetylase 6 (HDAC6) is an unique subtype of histone deacetylases with two tandem deacetylase domains and substrate specificity for non-histone proteins. It is involved in many important physiological and pathological processes and has become a promising therapeutic target in recent decades. Different kinds of potent HDAC6-selective inhibitors have been reported around the world. This paper reviews the progress in the study of structure and functions of HDAC6 as well as the development of HDAC6-selective inhibitors.
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