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Cytotoxic activities of the pyrimidine-based acetamide and isophthalimide derivatives: an in vitro and in silico studies

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dc.creator MUHAMMED, Muhammed Tılahun
dc.creator AKKOÇ, Senem
dc.creator KÖKBUDAK, ZÜLBİYE
dc.date 2023-01-01T00:00:00Z
dc.date.accessioned 2025-02-25T10:23:25Z
dc.date.available 2025-02-25T10:23:25Z
dc.identifier 662e897d-0484-4715-ac45-2ef230929bb0
dc.identifier 10.1080/08927022.2023.2202766
dc.identifier https://avesis.sdu.edu.tr/publication/details/662e897d-0484-4715-ac45-2ef230929bb0/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/99982
dc.description In here, a series of pyrimidin-(1(2H)-yl)acetamide and pyrimidin-(1(2H)-yl)isophthalimide derivatives were synthesised according to literature. The cytotoxic activity properties of these molecules were screened against human cancer cell lines as in vitro. The results demonstrated that these molecules had moderate effects on cancer cell lines for 48 h. The binding potential of the relatively active compound, ZF1, towards CDK1 (cyclin-dependent kinase 1) was investigated through molecular docking. The stability of the enzyme-ZF1 complex procured from the molecular docking was assessed through molecular dynamics (MD) simulation. Then, the electrochemical properties of the synthesised compounds were computed through density functional theory (DFT) studies. Computational pharmacokinetic analysis was also performed. The computational studies revealed that ZF1 could bind to CDK1 but its binding potential was less than the standard drug. The MD simulation exhibited that the compound could be stable inside the binding region during the simulation period. ZP3 is predicted to have the highest chemical stability among the synthesised compounds. Furthermore, the computational pharmacokinetic study revealed that ZP1, ZP2, and ZP3 had drug-like properties.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Cytotoxic activities of the pyrimidine-based acetamide and isophthalimide derivatives: an in vitro and in silico studies
dc.type info:eu-repo/semantics/article


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