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dc.creatorOmar, Kouatli
dc.creatorGeronikaki, Athina
dc.creatorZoumpoulakis, Panagiotis
dc.creatorCamoutsis, Charalabos
dc.creatorSoković, Marina
dc.creatorĆirić, Ana
dc.creatorGlamočlija, Jasmina
dc.date.accessioned2020-01-31T09:36:20Z
dc.date.available2020-01-31T09:36:20Z
dc.date.issued2010
dc.identifier.issn0968-0896
dc.identifier.urihttps://radar.ibiss.bg.ac.rs/handle/123456789/3588
dc.description.abstractAs part of ongoing studies in developing new antimicrobials, a class of structurally novel 4-thiazolidinone derivatives incorporating three known bioactive nuclei such as thiazole, thiazolidinone and adamantane was synthesized by the multi-step reaction protocol, already reported in the literature. NMR and Molecular Modeling techniques were employed for structure elucidation and Z/E potential isomerism configuration of the analogues. Evaluation of antibacterial and antifungal activity showed that almost all compounds exhibited better results than reference drugs thus they could be promising candidates for novel drugs.en
dc.publisherElsevier BVen
dc.rightsrestrictedAccess
dc.sourceBioorganic & Medicinal Chemistryen
dc.subject4-Thiazolidinone
dc.subjectAntibacterial
dc.subjectAntifungal
dc.subjectZ/E isomerism
dc.titleNovel 4-thiazolidinone derivatives as potential antifungal and antibacterial drugsen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractЦамоутсис, Цхаралабос; Ћирић, Aна; Соковић, Марина; Героникаки, Aтхина; Гламочлија, Јасмина; Омар, Коуатли; Зоумпоулакис, Панагиотис;
dc.rights.holder© 2009 Elsevier Ltd.
dc.citation.issue1
dc.citation.volume18
dc.identifier.doi10.1016/j.bmc.2009.10.041
dc.identifier.pmid19914077
dc.identifier.scopus2-s2.0-72149105339
dc.identifier.wos000272892100046
dc.citation.spage426
dc.citation.epage432
dc.type.versionpublishedVersion
dc.citation.rankM21


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