Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/54621
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dc.contributor.authorTrần, Phương Thảo-
dc.contributor.authorHoàng, Văn Hải-
dc.date.accessioned2021-06-09T02:52:17Z-
dc.date.available2021-06-09T02:52:17Z-
dc.date.issued2018-
dc.identifier.issn0866-7861-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/54621-
dc.description.abstractA new series of N-(4-methoxy-3-aminoalkyloxy-phenyl)thiourea were synthesized and their glutaminyl cyclase (QC) inhibitivity was fluorometrically evaluated The compounds were obtained via 6 or 7 steps by well-known reactions. Of these synthesized compounds, four (22-25) showed potential inhibitory activity on glutaminyl cyclase (QC) (ICX values of 9,026.8 nM).vi_VN
dc.language.isovivi_VN
dc.relation.ispartofseriesTạp chí Dược học;Số 509 .- Tr.33-36,87-
dc.subjectN-(4-Methoxy-3-aminoalkyloxy-phenyl)thioureavi_VN
dc.subjectThioureavi_VN
dc.subjectInhibitionvi_VN
dc.subjectGlutaminyl cyclasevi_VN
dc.titleTổng hợp và thử tác dụng ức chế enzym glutaminyl cyclase của một số dẫn chất N-(4-methoxy-3-aminoalkyloxy- phenyl) thiourea móivi_VN
dc.typeArticlevi_VN
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