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Design and synthesis of a tetrahydroisoquinoline-based hydroxamate derivative (ZYJ-34v), an oral active histone deacetylase inhibitor with potent antitumor activity

In our previous study we developed a novel series of tetrahydroisoquinoline-based hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors (Bioorg. Med. Chem., 2010, 18, 1761–1772., J. Med. Chem., 2011, 54, 2823–2838.), among which compound ZYJ-34c (1) was identified and validated as the...

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Autori principali: Zhang, Yingjie, Liu, Chunxi, Chou, C. James, Wang, Xuejian, Jia, Yuping, Xu, Wenfang
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3723752/
https://ncbi.nlm.nih.gov/pubmed/23581848
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cbdd.12144
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