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Discovery of histone deacetylase 3 (HDAC3)-specific PROTACs()

Histone deacetylases (HDACs) are validated drug targets for cancer treatment. Increased HDAC isozyme selectivity and novel strategies to inhibit HDAC activity could lead to safer and more effective drug candidates. Nonetheless, it is quite challenging to develop isozyme-specific HDACi due to the hig...

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Publicado en:Chem Commun (Camb)
Autores principales: Xiao, Yufeng, Wang, Jia, Zhao, Lisa Y., Chen, Xinyi, Zheng, Guangrong, Zhang, Xuan, Liao, Daiqing
Formato: Artigo
Lenguaje:Inglês
Publicado: 2020
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7654701/
https://ncbi.nlm.nih.gov/pubmed/32840532
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/d0cc03243c
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