Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/11651
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dc.contributor.authorMilić, Draganen
dc.contributor.authorKop T.en
dc.contributor.authorCsanadi J.en
dc.contributor.authorJuranic Z.en
dc.contributor.authorZizak Z.en
dc.contributor.authorGasic M.en
dc.contributor.authorSolaja B.en
dc.date.accessioned2020-03-03T14:45:14Z-
dc.date.available2020-03-03T14:45:14Z-
dc.date.issued2009-11-04en
dc.identifier.issn0039128Xen
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/11651-
dc.description.abstractA simple approach to a stable steroidal estrone derived A,B-spiro system is reported. Treatment of estrone derived A-ring diepoxyalcohol with the Ac2O-TMSOTf system at the ambient temperature led to acetylation, while at the reflux temperature the acid-catalysed rearrangement took place affording the spiro-compound. Results of extensive in vitro and in vivo anticancer tests on the diepoxide, as well as preliminary data on the antiproliferative activity of the spiro-product against three cancer cell lines, are also presented. © 2009 Elsevier Inc. All rights reserved.en
dc.relation.ispartofSteroidsen
dc.titleEstrone derived steroidal diepoxide: Biologically active compound and precursor of a stable steroidal A,B-spiro systemen
dc.typeJournal/Magazine Articleen
dc.identifier.doi10.1016/j.steroids.2009.06.002en
dc.identifier.pmid74en
dc.identifier.scopus2-s2.0-70049110807en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/70049110807en
dc.relation.lastpage895en
dc.relation.firstpage890en
dc.relation.issue12en
dc.relation.volume74en
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptPoljoprivredni fakultet, Departman za ekonomiku poljoprivrede i sociologiju sela-
crisitem.author.parentorgPoljoprivredni fakultet-
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