Design, synthesis, inhibiting HDACs ability and antitumor activity of pyrimidin-4(3H)-one hydroxamate derivatives-Reference-Cited by-同舟云学术

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Design, synthesis, inhibiting HDACs ability and antitumor activity of pyrimidin-4(3H)-one hydroxamate derivatives

Published:2016-06-14 Issue:4 Volume:32 Page:576-580
ISSN:1005-9040
Container-title:Chemical Research in Chinese Universities
language:en
Short-container-title:Chem. Res. Chin. Univ.

Author:

Lu Haibin,Jin Xiangqun,Jin Yang,Huang Bangrui,Wang Cheng,Wang Chunhe,Ma Fangyuan,Chen Yuting,Li Jiarui,Cong Yu,Wang Wenlong,Song Yuming,Mu Xupeng

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s40242-016-6105-7.pdf

Reference20 articles.

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2. Kristensen L. S., Nielsen H. M., Hansen L. L., Eur. J. Pharmacol., 2009, 625, 131

3. Hoshino I., Matsubara H., Surg. Today, 2010, 40(9), 809

4. Marks P., Rifkind R. A., Richon V. M., Breslow R., Miller T., Kelly W. K., Nat. Rev. Cancer, 2001, 1(3), 194

5. Bolden J. E., Peart M. J., Johnstone R. W., Nat. Rev. Drug Discov., 2006, 5(9), 769

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. Design, synthesis and biological evaluation of novel selective thiol-based histone deacetylase(HDAC) VI inhibitors bearing indeno[1,2-c]pyrazole or benzoindazole scaffold;Chemical Research in Chinese Universities;2018-01-02

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