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Design, Synthesis, Cytotoxic Activity, and In Silico Studies of New Schiff Bases Including Pyrimidine Core

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dc.creator Sahin, Onur
dc.creator KÖKBUDAK, ZÜLBİYE
dc.creator TÜRKMENOĞLU, BURÇİN
dc.creator AKKOÇ, Senem
dc.creator KARATAŞ, HALİS
dc.creator Aydin, Meltem
dc.date 2023-02-10T00:00:00Z
dc.date.accessioned 2025-02-25T10:33:17Z
dc.date.available 2025-02-25T10:33:17Z
dc.identifier 845bf645-9239-464f-bfcd-233f2eb4cb13
dc.identifier 10.1002/slct.202204221
dc.identifier https://avesis.sdu.edu.tr/publication/details/845bf645-9239-464f-bfcd-233f2eb4cb13/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/100385
dc.description © 2023 Wiley-VCH GmbH.In here, two new Schiff base molecules (3 and 4) were synthesized from the condensation reaction of 1-amino-5-benzoyl-4-phenylpyrimidine-2(1H)-one (1) and 1-amino-5-(4-methylbenzoyl)-4-p-tolylpyrimidin-2(1H)-one (2) with 4-bromobenzaldehyde. These molecules were completely characterized by IR, NMR, and HR-MS. Moreover, molecule 4 was determined by single crystal x-ray diffraction (SC-XRD) patterns. The crystallographic analysis revealed that molecule 4 crystallizes in the monoclinic system, space group P21/c. The molecules were screened in colon, lung and liver cell lines. The results showed that molecule 4 had cytotoxic activity in all screened cancer cell lines. Molecular docking studies of molecules 3 and 4, which were synthesized experimentally and whose cytotoxic activities were examined, were carried out with in silico approaches. Binding parameter values and active binding sites were determined by interacting the compounds with EGFR (PDB ID : 1M17) and VEGFR-2 (PDB ID : 4ASD) crystal structures, respectively, in molecular docking. In addition, the theoretical pharmacokinetic properties of compounds 3 and 4 were evaluated using ADME analysis.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Design, Synthesis, Cytotoxic Activity, and In Silico Studies of New Schiff Bases Including Pyrimidine Core
dc.type info:eu-repo/semantics/article


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