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dc.contributor.authorDuong T. Anh-
dc.contributor.authorPham-The Hai-
dc.contributor.authorLe D. Huy-
dc.contributor.authorHoang B. Ngoc-
dc.contributor.authorTrinh T. M. Ngoc-
dc.contributor.authorDo T. M. Dung-
dc.contributor.authorEun J. Park-
dc.contributor.authorIn K. Song-
dc.contributor.authorJong S. Kang-
dc.contributor.authorJoo-Hee Kwon-
dc.contributor.authorTruong T. Tung-
dc.contributor.authorSang-Bae Han-
dc.contributor.authorNguyen-Hai Nam-
dc.date.accessioned2021-09-10T04:46:53Z-
dc.date.available2021-09-10T04:46:53Z-
dc.date.issued2021-
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/acsomega.0c05870-
dc.identifier.urihttps://dlib.phenikaa-uni.edu.vn/handle/PNK/2748-
dc.description.abstractTwo series of novel 4-oxoquinazoline-based N-hydroxypropenamides (9a–m and 10a–m) were designed, synthesized, and evaluated for their inhibitory and cytotoxicity activities against histone deacetylase (HDAC). The compounds showed good to potent HDAC inhibvi
dc.language.isoengvi
dc.publisherAmerican Chemical Societyvi
dc.titleNovel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluationvi
dc.typeBài tríchvi
eperson.identifier.doihttps://doi.org/10.1021/acsomega.0c05870-
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