Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/22486
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dc.contributor.authorPetronijević, Jelena-
dc.contributor.authorJoksimović N.-
dc.contributor.authorKostic, Marina-
dc.contributor.authorDivac, Vera-
dc.contributor.authorJanković, Nenad-
dc.date.accessioned2025-08-05T12:17:29Z-
dc.date.available2025-08-05T12:17:29Z-
dc.date.issued2018-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/22486-
dc.description.abstractIn order to investigate new potential therapeutically active agents, we investigated the biological properties of two small libraries of quinoxalinones and 3,4-dihydro-2(1H)-quinoxalinones (Fig. 1). The results obtained showed that compounds 5, 9–11 have good cytotoxic activity against HeLa cells where the lowest IC50 ǀalue ;ϭϬ.ϰϲ ± Ϭ.ϴϮ μM/ŵLͿ ǁas measured for compound 10. Additionally, the most active compounds (5, 9–11) showed much better selectivity for MRC-5 cells (up to 17.4) compared to cisplatin. In vitro evaluation of the iŶhiďitioŶ of the eŶzLJŵe α-glucosidase showed that compounds 10 and 11 exert significant iŶhiďitioŶ of the eŶzLJŵe at ϱϮ.ϱϰ ± Ϭ.Ϭϵ aŶd ϰϬ.Ϭϵ ± Ϭ.ϰϵ μM, ƌespeĐtiǀelLJ.en_US
dc.language.isoenen_US
dc.rightsCC0 1.0 Universal*
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/*
dc.subjectquinoxalinonesen_US
dc.subject3,4-dihydro-2(1H)-quinoxalinonesen_US
dc.subjectbiological activityen_US
dc.titleBiological evaluation of the 3,4-dihydro-2(1H)-quinoxalinones and 3,4-dihydro-1,4-benzoxazin-2-onesen_US
dc.typeconferenceObjecten_US
dc.description.versionPublisheden_US
dc.type.versionPublishedVersionen_US
dc.source.conference55th Meeting of the Serbian Chemical Society, 2018, Novi Sad, Serbiaen_US
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