Discovery of potent small molecule inhibitors of histone lysine methyltransferase NSDs-Reference-Cited by-同舟云学术

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Discovery of potent small molecule inhibitors of histone lysine methyltransferase NSDs

Published:2024-03 Issue: Volume:268 Page:116264
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Piao Lianhua,Gao Ying,Xu Xiaoshuang,Su Yangyang,Wang Yanong Daniel,Zhou Jie,Gao Yang,Fang Jin,Li Qihui,Chang Shan,Kong Ren

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Reference46 articles.

1. Role for the nuclear receptor-binding SET domain protein 1 (NSD1) methyltransferase in coordinating lysine 36 methylation at histone 3 with RNA polymerase II function;Lucio-Eterovic;Proc. Natl. Acad. Sci. U. S. A.,2010

2. The Brd4 extraterminal domain confers transcription activation independent of pTEFb by recruiting multiple proteins, including NSD3;Rahman;Mol. Cell Biol.,2011

3. Understanding the language of Lys36 methylation at histone H3;Wagner;Nat. Rev. Mol. Cell Biol.,2012

4. Histone lysine methyltransferase Wolf-Hirschhorn syndrome candidate 1 is involved in human carcinogenesis through regulation of the Wnt pathway;Toyokawa;Neoplasia,2011

5. The histone methyltransferase and putative oncoprotein MMSET is overexpressed in a large variety of human tumors;Hudlebusch;Clin. Cancer Res.,2011

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. Discovery of a Highly Potent and Selective Inhibitor Targeting Protein Lysine Methyltransferase NSD2;Journal of Medicinal Chemistry;2024-09-04

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