Synthesis of the 3,5-diphenyl-1H-pyrazole and cytogenetic and oxidative alterations after exposure of cultured human whole blood cells

E. Akbas, F. Çelikezen, H. Turkez, O. Ozdemir, Adem Ruzgar, Erdem Ergan, E. Şahin
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引用次数: 3

Abstract

Abstract The 3,5-diphenyl-1H-pyrazole was obtained by condensation reaction of dibenzoylmethane and thiosemicarbazide in acetic acid under conventional heating and microwave irradiation method. The structure of the 3,5-diphenyl-1H-pyrazole confirmed by IR, 1H, and 13C NMR and X-ray diffraction and the geometry optimization was carried out using density functional theory (DFT) methods at B3LYP/6-31G, 6-31G(d), 6-31G(d, p), 6-311G(d, p), 6-311G(2d, 2p), 6-31+G(d, p), 6-311++G(d, p) levels. In addition, cytotoxic and oxidative effects were investigated in cultured human peripheral blood cells.
3,5-二苯基-1H-吡唑的合成及其暴露于培养的人全血细胞后的细胞遗传学和氧化变化
摘要以二苯甲酰基甲烷和缩氨基硫脲为原料,在常规加热和微波辐射的条件下,在乙酸中缩合得到3,5-二苯基-1H-吡唑。利用密度泛函理论(DFT)方法,在B3LYP/6-31G、6-31G(d,p)、6-311G(d,p)、6-311 G(2d,2p)、6-31+G(d、p)、6~311+G(d)、6~131+G(p)水平上,通过IR、1H、13C NMR和X射线衍射证实了3,5-二苯基-1H-吡唑的结构和几何结构优化。此外,研究了培养的人外周血细胞的细胞毒性和氧化作用。
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Cogent Chemistry
Cogent Chemistry CHEMISTRY, MULTIDISCIPLINARY-
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