Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29348
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dc.contributor.authorStasevych, Maryna-
dc.contributor.authorZvarych, Viktor-
dc.contributor.authorLunin, Volodymyr-
dc.contributor.authorDeniz, Nahide Gülşah-
dc.contributor.authorGökmen, Zeliha-
dc.contributor.authorUlukaya, Engin-
dc.contributor.authorPoroikov, V.-
dc.contributor.authorGloriozova, Tatyana-
dc.contributor.authorNovikov, Volodymyr-
dc.date.accessioned2022-11-03T10:54:30Z-
dc.date.available2022-11-03T10:54:30Z-
dc.date.issued2017-04-24-
dc.identifier.citationStasevych, M. vd. (2017). ''Computer-aided prediction and cytotoxicity evaluation of dithiocarbamates of 9,10-anthracenedione as new anticancer agents''. SAR and QSAR in Environmental Research, 28(5), 355-366.en_US
dc.identifier.issn1062-936X-
dc.identifier.issn1029-046X-
dc.identifier.urihttps://doi.org/10.1080/1062936X.2017.1323796-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/1062936X.2017.1323796-
dc.identifier.urihttp://hdl.handle.net/11452/29348-
dc.description.abstractAnticancer activity as an associated action for a series of dithiocarbamates of 9,10-anthracenedione was predicted using the PASS computer program and analysed with PharmaExpert software. The predicted cytotoxic activity of the dithiocarbamate derivatives of 9,10-anthracenedione was evaluated in vitro on cancer cells of the human lung (A549), prostate (PC3), colon (HT29) and human breast (MCF7) using the sulforhodamine B (SRB) cell viability assay. Among these compounds, 9,10-dioxo-9,10-dihydroanthracen-1-yl pyrrolidin-1-carbodithioate and 9,10-dioxo-9,10-dihydroanthracen-2-yl pyrrolidin-1-carbodithioate were identified as the most potent anticancer agents with cytotoxic activity against the MCF-7 human breast cell line with GI(50) values of 1.40 M and 1.52 M, whereas the GI(50) value for the reference anticancer drug mitoxantrone was 3.93 M. Thus, anticancer activity predicted by PASS with a probability Pa > 30% was confirmed by the experiment. Relatively small Pa values estimated by PASS indicated the novelty of the considered derivatives comparing to the compounds from the PASS training set.en_US
dc.description.sponsorshipMinistry of Education and Science of Ukraine, Scientific Research Project - 0116U004138en_US
dc.description.sponsorshipİstanbul Üniversitesi - NP-45621tr_TR
dc.description.sponsorshipRussian State Academies of Sciences Fundamental Research Programen_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChemistryen_US
dc.subjectComputer scienceen_US
dc.subjectEnvironmental sciences & ecologyen_US
dc.subjectMathematical & computational biologyen_US
dc.subjectToxicologyen_US
dc.subjectAnticancer activityen_US
dc.subjectCell line cytotoxicity predictoren_US
dc.subjectcomputer-aided predictionen_US
dc.subjectDithiocarbamates of 9, 10-anthracenedioneen_US
dc.subjectPASSen_US
dc.subjectPharmaExperten_US
dc.subjectDerivativesen_US
dc.subjectChemistryen_US
dc.subject.meshA549 cellsen_US
dc.subject.meshAnthraquinonesen_US
dc.subject.meshAntineoplastic agentsen_US
dc.subject.meshCell Survivalen_US
dc.subject.meshDrug screening assays, antitumoren_US
dc.subject.meshHT29 cellsen_US
dc.subject.meshHumansen_US
dc.subject.meshMCF-7 cellsen_US
dc.subject.meshQuantitative structure-activity relationshipen_US
dc.subject.meshRhodaminesen_US
dc.subject.meshSoftwareen_US
dc.subject.meshThiocarbamatesen_US
dc.subject.meshTumor cells, cultureden_US
dc.titleComputer-aided prediction and cytotoxicity evaluation of dithiocarbamates of 9,10-anthracenedione as new anticancer agentsen_US
dc.typeArticleen_US
dc.identifier.wos000402994100001tr_TR
dc.identifier.scopus2-s2.0-85019597292tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyet Fakültesi/Biyoloji Bölümü.tr_TR
dc.contributor.orcid0000-0002-8410-1786tr_TR
dc.identifier.startpage355tr_TR
dc.identifier.endpage366tr_TR
dc.identifier.volume28tr_TR
dc.identifier.issue5tr_TR
dc.relation.journalSAR and QSAR in Environmental Researchen_US
dc.contributor.buuauthorAkgün, Oğuzhan-
dc.contributor.researcheridA-5608-2019tr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed28524703tr_TR
dc.subject.wosChemistry, multidisciplinaryen_US
dc.subject.wosComputer science, interdisciplinary applicationsen_US
dc.subject.wosEnvironmental sciencesen_US
dc.subject.wosMathematical & computational biologyen_US
dc.subject.wosToxicologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.contributor.scopusid57194269996tr_TR
dc.subject.scopusProtein Tyrosine Kinase; Sodium Nitrite; Triazolesen_US
dc.subject.emtree9,10-anthraquinoneen_US
dc.subject.emtreeAnthraquinone derivativeen_US
dc.subject.emtreeAantineoplastic agenten_US
dc.subject.emtreeLissamine rhodamine Ben_US
dc.subject.emtreeRhodamineen_US
dc.subject.emtreeThiocarbamic acid derivativeen_US
dc.subject.emtreeA-549 cell lineen_US
dc.subject.emtreeCell survivalen_US
dc.subject.emtreeChemistryen_US
dc.subject.emtreeDrug effectsen_US
dc.subject.emtreeDrug screeningen_US
dc.subject.emtreeHT-29 cell lineen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMCF-7 cell lineen_US
dc.subject.emtreeQquantitative structure activity relationen_US
dc.subject.emtreeSoftwareen_US
dc.subject.emtreeT tumor cell cultureen_US
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