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DC Field | Value | Language |
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dc.contributor.author | Lauro, Figueroa-VaIverde | - |
dc.contributor.author | Maria, Lopez-Ramos | - |
dc.contributor.author | Francisco, Diaz-Cedillo | - |
dc.contributor.author | Marcela, Rosas-Nexticapa | - |
dc.contributor.author | Virginia, Mateu-Armand | - |
dc.contributor.author | E., Alejandra Garcimarero-Espino | - |
dc.contributor.author | Yazmin, Ortiz-Ake | - |
dc.date.accessioned | 2020-06-19T06:42:27Z | - |
dc.date.available | 2020-06-19T06:42:27Z | - |
dc.date.issued | 2020 | - |
dc.identifier.issn | 2525-2321 | - |
dc.identifier.uri | http://dspace.ctu.edu.vn/jspui/handle/123456789/25571 | - |
dc.description.abstract | Several 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.iso | en | vi_VN |
dc.relation.ispartofseries | Vietnam Journal of Chemistry;Số 58(01) .- Tr.10-19 | - |
dc.subject | Azetidine | vi_VN |
dc.subject | Derivatives | vi_VN |
dc.subject | Etherification and addition | vi_VN |
dc.subject | Biological activity | vi_VN |
dc.title | Design and synthesis of new azetidine-steroid derivative with inotropic activity in a heart failure model | vi_VN |
dc.type | Article | vi_VN |
Appears in Collections: | Vietnam Journal of Chemistry |
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_file_ Restricted Access | 3.11 MB | Adobe PDF | ||
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