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dc.contributor.authorDo, Thi Mai Dung-
dc.contributor.authorEun, Jae Park-
dc.contributor.authorDuong, Tien Anh-
dc.contributor.authorPham, The Hai-
dc.contributor.authorLe, Quang Bao-
dc.date.accessioned2022-05-05T07:26:13Z-
dc.date.available2022-05-05T07:26:13Z-
dc.date.issued2022-
dc.identifier.urihttps://www.eurekaselect.com/article/120263-
dc.identifier.urihttps://dlib.phenikaa-uni.edu.vn/handle/PNK/5726-
dc.description.abstractHerein, we have designed and synthesized a series of the novel (E)-N'-((1-(4-chlorobenzyl)- 1H-indol-3-yl)methylene)-2-(4-oxoquinazolin-3(4H)-yl)acetohydrazides (5) as potent small molecules activating procaspase- 3. The compounds were designed by the amalgamation of structural features of PAC-1 (the first procaspase-3 activator) and oncrasin-1, one potential anticancer agentvi
dc.language.isoenvi
dc.publisherBentham Science Publishersvi
dc.subjectAcetohydrazides-
dc.subjectQuinazolin-4(3H)-one
dc.titleDesign, Synthesis and Evaluation of Novel (E)-N'-((1-(4-chlorobenzyl)-1H-indol-3- yl)methylene)-2-(4-oxoquinazolin-3(4H)-yl)acetohydrazides as Antitumor Agentsvi
dc.typeBài tríchvi
eperson.identifier.doihttp://dx.doi.org/10.2174/1871520622666220118154914-
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