Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/1494
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dc.contributor.authorBligh, Annie Sim Wanen_US
dc.date.accessioned2021-10-11T03:58:04Z-
dc.date.available2021-10-11T03:58:04Z-
dc.date.issued2014-
dc.identifier.urihttps://repository.cihe.edu.hk/jspui/handle/cihe/1494-
dc.description.abstractA series of novel hexa-arm star shaped thiosemicarbazones with different substitutions at <i>para</i> positions emanating from cyclotriphosphazene core were prepared with excellent yields. The structure of all the synthesized compounds was confirmed by elemental analysis and spectroscopic methods (FT-IR, <sup>1</sup>H, <sup>13</sup>C, <sup>31</sup>P NMR, 2D HSQC and ESI-MS). The compounds were evaluated for their <i>in vitro</i> antiproliferative activity against breast cancer (MCF7) and ovarian cancer (PA-1) cell lines using MTT assay. The newly synthesized compounds exhibited moderate to good activity against the tested cell lines. Among them the halo substituted benzoic thiosemicarbazones were found to be more potent towards anticancer activity.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofInorganica Chimica Actaen_US
dc.titleSynthesis, characterization and antiproliferative activity of hexa arm star shaped thiosemicarbazones derived from cyclotriphosphazene coreen_US
dc.typejournal articleen_US
dc.identifier.doi10.1016/j.ica.2014.06.040-
dc.contributor.affiliationSchool of Health Sciencesen_US
dc.relation.issn0020-1693en_US
dc.description.volume421en_US
dc.description.startpage459en_US
dc.description.endpage464en_US
dc.cihe.affiliatedNo-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.openairetypejournal article-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.languageiso639-1en-
crisitem.author.deptSchool of Health Sciences-
crisitem.author.orcid0000-0002-4757-2159-
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