Quantitative Structure–Activity Relationship Studies on Hydroxamic Acids Acting as Histone Deacetylase Inhibitors
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-38111-9_8
Reference68 articles.
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3. Bieliauskas AV, Weerasinghe SVW, Pflum MKH (2007) Structural requirements of HDAC inhibitors: SAHA analogs functionalized adjacent to the hydroxamic acid. Bioorg Med Chem Let 17:2216–2219
4. Bouchain G, Leit S, Frechette S et al (2003) Development of potential antitumor agents. Synthesis and biological evaluation of a new set of sulfonamide derivatives as histone deacetylase inhibitors. J Med Chem 46:820–830
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Cited by 2 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. Quantitative structure–activity relationship analysis and virtual screening studies for identifying HDAC2 inhibitors from known HDAC bioactive chemical libraries;SAR and QSAR in Environmental Research;2017-02-28
2. QSAR Studies on Hydroxamic Acids: A Fascinating Family of Chemicals with a Wide Spectrum of Activities;Chemical Reviews;2015-05-29
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