Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/25571
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dc.contributor.authorLauro, Figueroa-VaIverde-
dc.contributor.authorMaria, Lopez-Ramos-
dc.contributor.authorFrancisco, Diaz-Cedillo-
dc.contributor.authorMarcela, Rosas-Nexticapa-
dc.contributor.authorVirginia, Mateu-Armand-
dc.contributor.authorE., Alejandra Garcimarero-Espino-
dc.contributor.authorYazmin, Ortiz-Ake-
dc.date.accessioned2020-06-19T06:42:27Z-
dc.date.available2020-06-19T06:42:27Z-
dc.date.issued2020-
dc.identifier.issn2525-2321-
dc.identifier.urihttp://dspace.ctu.edu.vn/jspui/handle/123456789/25571-
dc.description.abstractSeveral steroid derivatives have prepared as inotropic drugs; however, there are few reports on azetidine-steroid derivatives with inotropic activity. The aim of this study was to synthesize four azetidine-steroid derivatives (compounds 3 to 6) to evaluate their biological activity on left ventricular pressure. The first stage was achieved by preparation of azetidine-derivatives using reactions of etherification and addition. The second stage involves the evaluation of biological activity from azetidine derivatives on left ventricular pressure in a heart failure model using estrone as control. The results showed that only compound 3 increases left ventricular pressure compared with estrone, compounds 2 and 4 to 6. In conclusion, the positive inotropic effect exerted by compound 3 depends on the functional groups involved in their Chemical structure.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesVietnam Journal of Chemistry;Số 58(01) .- Tr.10-19-
dc.subjectAzetidinevi_VN
dc.subjectDerivativesvi_VN
dc.subjectEtherification and additionvi_VN
dc.subjectBiological activityvi_VN
dc.titleDesign and synthesis of new azetidine-steroid derivative with inotropic activity in a heart failure modelvi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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