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Investigation of structural, electronical and in vitro cytotoxic activity properties of some heterocyclic compounds

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dc.creator Ozalp, Ayhan
dc.creator TÜZÜN, BURAK
dc.creator AKKOÇ, SENEM
dc.creator KÖKBUDAK, ZÜLBİYE
dc.date 2021-12-01T00:00:00Z
dc.date.accessioned 2021-12-03T11:20:31Z
dc.date.available 2021-12-03T11:20:31Z
dc.identifier 3e1b297b-d060-4b55-9074-e4e4bcece0ac
dc.identifier 10.1016/j.molstruc.2021.131127
dc.identifier https://avesis.sdu.edu.tr/publication/details/3e1b297b-d060-4b55-9074-e4e4bcece0ac/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/91069
dc.description A series of heterocyclic compounds (15) were synthesized, characterized and tested towards two human cancer cell lines for learning their in vitro antiproliferative activities. Compound 3 demonstrated the most promising activity in breast cancer cell line with a half maximal inhibitory concentration (IC50) value of 23.73 mu M compared to other compounds (1, 2, 4, 5). Cytotoxic activity studies revealed that compounds 24 did not have antiproliferative activity towards liver cancer cell line. Computational methods were used to determine various quantum chemical parameters in order to identify correlations with the measured biological activity, which can assist in the molecular modeling of new heterocyclic systems. The biological activities of heterocyclic molecules against cancer cell proteins that are the crystal structure of the BRCT repeat region from the breast cancer-associated protein, ID: 1JNX, crystal structure of VEGFR kinase (liver cancer) protein, ID: 3WZE, and crystal structure of an allosteric Eya2 phosphatase inhibitor (lung cancer) protein, ID: 5ZMA, were compared. Finally, ADME/T analysis was performed for heterocyclic molecules and their future possibilities as a drug were investigated. (C) 2021 Elsevier B.V. All rights reserved.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Investigation of structural, electronical and in vitro cytotoxic activity properties of some heterocyclic compounds
dc.type info:eu-repo/semantics/article


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