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Article 2024 · 5 citations

Synthesis and Biological Evaluation of Novel Benzylidene Thiazolo Pyrimidin-3(5<i>H</i>)-One Derivatives

Akbas, Esvet, Othman, Khdir A., Celikezen, Fatih Caglar, Ejder, Nebahat Aydogan, Turkez, Hasan, Yapca, Omer Erkan, Mardinoglu, Adil

Abstract

Starting compound 1 was synthesized according to reference.(1) Benzylidene thiazole pyrimidin-3(5H)-ones were synthesized reactions of 1 with bromoacetic acid and various aryl-aldehydes in the same vessel via one-step, unlike studies in the literature. Quantum chemical parameters and full geometry optimizations for all compounds were computed using DFT based on B3LYP. Cytotoxic action potential of synthesized compounds was evaluated using trypan blue dye exclusion and MTT assays in different cell lines including adenocarcinoma alveolar basal epithelial-like adherent A549 cells, the colon adenocarcinoma HT-29 cells, prostate adenocarcinoma DU-145 cells, and diploid ARPE-19 retinal pigment epithelial cells. Embryotoxicity and genotoxicity assessments were performed on pluripotent human embryonal carcinoma NT2 and human lymphocyte cells, respectively. Compound A1 exhibited good anticancer activity on A549 and DU-145 cell lines, and the compounds including A3, 4, 6, and 9 induced cytotoxicity on A549 cells. The compounds A1-10 also showed a good biosafety profile at relatively lower concentrations.

Keywords
Pyrimidine theoretical chemistry MCR cytotoxicity anticarcinogenic effect genotoxicity PYRIMIDINE-DERIVATIVES ANTICANCER INHIBITION DFT ANTIOXIDANT DESIGN
WoS Categories
Chemistry, Organic
Sustainable Development Goals
Citation
Journal
POLYCYCLIC AROMATIC COMPOUNDS
Year
2024
Volume
44
Issue
5
Pages
3061-3078
ISSN
1040-6638
eISSN
1563-5333
DOI
10.1080/10406638.2023.2228961
WoS UID
WOS:001030887700001
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