Akbas, EsvetCelikezen, Fatih CaglarTurkez, HasanOzdemir, OzlemRuzgar, AdemErgan, ErdemSahin, Ertan2025-05-102025-05-1020172331-200910.1080/23312009.2017.1344115https://doi.org/10.1080/23312009.2017.1344115https://hdl.handle.net/20.500.14720/12009The 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, H-1, and C-13 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.eninfo:eu-repo/semantics/openAccessPyrazoleThiosemicarbazideCytotoxicArticle31N/AN/AWOS:000404846100001