Design, synthesis, and biological evaluation of HDAC6 inhibitors targeting L1 loop and serine 531 residue-Reference-Cited by-同舟云学术

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Design, synthesis, and biological evaluation of HDAC6 inhibitors targeting L1 loop and serine 531 residue

Published:2024-02 Issue: Volume:265 Page:116057
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Jha Sonam,Kim Ji Hyun,Kim Mikyung,Nguyen Ai-Han,Ali Khan Hashim,Gupta Sunil K.,Park Sun You,Ha Eunyoung,Seo Young Ho

Funder

Ministry of Education

National Research Foundation of Korea

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference43 articles.

1. Histone post-translational modifications — cause and consequence of genome function;Millán-Zambrano;Nat. Rev. Genet.,2022

2. Metabolic regulation of histone post-translational modifications;Fan;ACS Chem. Biol.,2015

3. Histone acetyltransferases and deacetylases: molecular and clinical implications to gastrointestinal carcinogenesis;Sun;Acta Biochim. Biophys. Sin.,2012

4. Histone deacetylase 6 plays a role as a distinct regulator of diverse cellular processes;Li;FEBS J.,2013

5. Design, synthesis and biological evaluation of 3, 4-disubstituted-imidazolidine-2, 5-dione derivatives as HDAC6 selective inhibitors;Liang;Eur. J. Med. Chem.,2021

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. HDAC6 mediates tumorigenesis during mitosis and the development of targeted deactivating agents;Bioorganic Chemistry;2024-09

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