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Design, Synthesis and Biological Evaluation of Novel Coumarin-Based Hydroxamate Derivatives as Histone Deacetylase (Hdac) Inhibitors with Antitumor Activities

A series of novel coumarin-based hydroxamate derivatives were designed and synthesized as histone deacetylase inhibitors (HDACis). Selective compounds showed a potent HDAC inhibition with nM IC(50) values, with the best compound (10e) being nearly 90 times more active than vorinostat (SAHA) against...

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Bibliografski detalji
Izdano u:Molecules
Glavni autori: Yang, Feifei, Zhao, Na, Song, Jiali, Zhu, Kongkai, Jiang, Cheng-shi, Shan, Peipei, Zhang, Hua
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2019
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6680717/
https://ncbi.nlm.nih.gov/pubmed/31311163
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules24142569
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