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Histone deacetylase 6: structure, functions and development of selective inhibitors / 药学学报
Acta Pharmaceutica Sinica ; (12): 7-14, 2015.
Artículo en Chino | WPRIM | ID: wpr-251825
ABSTRACT
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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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Especificidad por Sustrato / Química / Inhibidores de Histona Desacetilasas / Histona Desacetilasas Límite: Humanos Idioma: Chino Revista: Acta Pharmaceutica Sinica Año: 2015 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Especificidad por Sustrato / Química / Inhibidores de Histona Desacetilasas / Histona Desacetilasas Límite: Humanos Idioma: Chino Revista: Acta Pharmaceutica Sinica Año: 2015 Tipo del documento: Artículo