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dc.creatorOpsenica, Dejan M.
dc.creatorAngelovski, G
dc.creatorPocsfalvi, G
dc.creatorJuranić, Z.
dc.creatorŽižak, Željko S.
dc.creatorKyle, D
dc.creatorMilhous, WK
dc.creatorŠolaja, Bogdan A.
dc.date.accessioned2018-11-22T00:06:14Z
dc.date.available2018-11-22T00:06:14Z
dc.date.issued2003
dc.identifier.issn0968-0896
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/559
dc.description.abstractSeveral cis and trans bis-steroidal 1,2,4,5-tetraoxanes possessing amide terminus were synthesised and evaluated as antimalarials and antiproliferatives. The compounds exhibited submicromolar antimalarial activity against Plasmodium falciparum D6 and W2 strains. The existence of HN-C(O) moiety was found necessary for pronounced antimalarial and antiproliferative activity. In antiproliferative screen, the trans tetraoxane 6 was found to exhibit a pronounced cytotoxicity on 14 cancer cell lines. In addition, tetraoxanes 11 and 12 exhibited significant cytotoxic activity too; microscopic examination of treated HeLa cells showed morphological appearance reminiscent for apoptosis (condensed and/or fragmented nuclei). (C) 2003 Elsevier Science Ltd. All rights reserved.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.rightsrestrictedAccess
dc.sourceBioorganic and Medicinal Chemistry
dc.titleAntimalarial and antiproliferative evaluation of bis-steroidal tetraoxanesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractМилхоус, WК; Кyле, Д; Поцсфалви, Г; Шолаја, Богдан A.; Јураниц, З; Зизак, З; Aнгеловски, Г; Опсеница, Р;
dc.citation.volume11
dc.citation.issue13
dc.citation.spage2761
dc.citation.epage2768
dc.identifier.wos000183590100011
dc.identifier.doi10.1016/S0968-0896(03)00224-4
dc.citation.other11(13): 2761-2768
dc.citation.rankM21
dc.identifier.pmid12788350
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-0037871977


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