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Article 2024 · 3 citations

Synthesis, Characterization, Theoretical Studies and in Vitro Embriyotoxic, Genotoxic and Anticancer Effects of Novel Phenyl(1,4,6-Triphenyl-2-Thioxo-1,2,3,4-Tetrahydropyrimidin-5-yl)Methanone

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

Abstract

In this study, phenyl (1,4,6-triphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methanone was obtained by using the Biginelli reaction method. The structure of this compound was analyzed using elemental analysis, IR, 1H, and 13C NMR. The quantum chemical calculations (QCC) of this compound were performed density functional theory (DFT) method, 6-31 G (d, p) base set, and B3LYP functions with the Gaussian09W software package. Literature shows that pyrimidine-derived compounds have very active biological properties. For this reason, the biologically active properties of the synthesized compound were also examined. To determine embryotoxic, genotoxic, and cytotoxic effects of compound, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT), lactate dehydrogenase (LDH) release, micronucleus (MN) and 8-OH-dG assays were carried out. On the other hand, pharmacokinetic and toxicity properties (ADMET) were predicted in silico via SwissADME and Protox-II web tools. In silico estimates of this compound used in the study showed that the compound has the covetable physicochemical properties for bioavailability. In conclusion, the obtained results of our study clearly showed that this compound exerted strong toxicity potential.

Keywords
Pyrimidin embryotoxicity genotoxicity cytotoxicity theoretical chemistry DFT PYRIMIDINE-DERIVATIVES BIOLOGICAL EVALUATION BRAIN PENETRATION MOLECULAR-SURFACE DRUG ABSORPTION DESIGN SOLUBILITY COMBINATORIAL PREDICTION RESISTANCE
WoS Categories
Chemistry, Organic
Sustainable Development Goals
Citation
Journal
POLYCYCLIC AROMATIC COMPOUNDS
Year
2024
Volume
44
Issue
9
Pages
6284-6301
ISSN
1040-6638
eISSN
1563-5333
DOI
10.1080/10406638.2023.2276243
WoS UID
WOS:001093481400001
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