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DC Field | Value | Language |
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dc.contributor.author | Duong T. Anh | - |
dc.contributor.author | Pham-The Hai | - |
dc.contributor.author | Le D. Huy | - |
dc.contributor.author | Hoang B. Ngoc | - |
dc.contributor.author | Trinh T. M. Ngoc | - |
dc.contributor.author | Do T. M. Dung | - |
dc.contributor.author | Eun J. Park | - |
dc.contributor.author | In K. Song | - |
dc.contributor.author | Jong S. Kang | - |
dc.contributor.author | Joo-Hee Kwon | - |
dc.contributor.author | Truong T. Tung | - |
dc.contributor.author | Sang-Bae Han | - |
dc.contributor.author | Nguyen-Hai Nam | - |
dc.date.accessioned | 2021-09-10T04:46:53Z | - |
dc.date.available | 2021-09-10T04:46:53Z | - |
dc.date.issued | 2021 | - |
dc.identifier.uri | https://pubs.acs.org/doi/abs/10.1021/acsomega.0c05870 | - |
dc.identifier.uri | https://dlib.phenikaa-uni.edu.vn/handle/PNK/2748 | - |
dc.description.abstract | Two 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 inhib | vi |
dc.language.iso | eng | vi |
dc.publisher | American Chemical Society | vi |
dc.title | Novel 4-Oxoquinazoline-Based N-Hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis, and Biological Evaluation | vi |
dc.type | Bài trích | vi |
eperson.identifier.doi | https://doi.org/10.1021/acsomega.0c05870 | - |
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