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Öğe Benzenesulfonamide based 1,3,4-oxadiazole derivatives: synthesis, pharmacokinetic property prediction, bovine carbonic anhydrase activity and molecular docking studies(Taylor & Francis Ltd, 2024) Alpinar, E.; Kaya, M. O.; Gulec, O.; Demirci, T.; Kaya, Y.; Arslan, M.Sulphur-containing compounds are highly significant as they can possess a variety of biological activities that make them useful for pharmacological purposes and for the mechanism by which drugs such as antibiotics bind to and disrupt bacterial cell walls. In this study, novel thioalkyl substituted-1,3,4 oxadiazole-bearing sulfonamide compounds have been successfully synthesized and characterized by (HNMR)-H-1, (CNMR)-C-13, IR and elemental analysis. The effects of different thioalkyl groups on the 1,3,4 oxadiazole group, the IC(5)0 value for Bovine Carbonic Anhydrase (BCA) found by in vitro, density functional theory (DFT) calculations, pharmacokinetics prediction and molecular docking are aimed to reveal the interactions on BCA. Firstly, pharmacokinetic predictions of thioalkyl substituted 1,3,4-oxadiazole compounds were generated to predict their potential hazards. Secondly, the predicted molecular docking data and 2D interaction were analyzed based on the best configuration from DFT optimization. Finally, the inhibition against BCA was analyzed in vitro and compared with the theoretical data. The compound (5o) has the best value such as IC50 = 51.80 mu M, HOMO-LUMO (Delta E 4.488 Ev), Delta G -7.69 kcal/mol, Full fitness -2152.72 FF and predicted toxicity results showed no significant results except hepatotoxicity. [GRAPHICAL ABSTRACT]Öğe Novel tetrazole and 1,3,4-oxadiazole derivatives synthesis, molecular docking, Adme, potential activator for rabbit muscle pyruvate kinase(Babes-Bolyai University, 2024) Kaya, M.O.; Demirci, T.; Karipçin, S.; Özdemir, O.; Kaya, Y.; Arslan, M.The activation of muscle pyruvate kinase (PK) increases the conversion of phosphoenolpyruvate (PEP) to pyruvate, which results in the production of ATP. This is critical for supplying the energy needed for muscle contraction. In this study, we synthesized 1,4-dihydropyridine/pyridine compounds bearing tetrazole and 1,3,4-oxadiazole groups by using Hantzsch method and characterized by FT-IR spectroscopy, elemental analysis, and 1 H and13C NMR and studied PK activation, ADME, and molecular docking. The studies revealed that all original synthesized compounds activated PK and AC50 (half-maximal activating concentration) values of the compounds were extremely effective (1.30 µM to 14.65 µM). © 2024, Babes-Bolyai University. All rights reserved.Öğe Performance analysis of hybrid Quantum Dots Sensitized Solar Cells consisting of CdS/CdX (X = Se, Te, SeTe) QD and Bromophenol Blue dye(Elsevier B.V., 2021) Elibol, E.; Demirci, T.In this study, the effects of hybrid associate consisting of CdX (X = Te, Se, SeTe) Quantum Dots (QD) and Bromophenol Blue (BPB) organic dye on hybrid Quantum Dots Sensitized Solar Cells (QDSSCs) design were investigated. In the study QDs were synthesized in the 604–623 nm emission range in order to be compatible with the absorbance range of the BPB, and mercaptopropionic acid (MPA) was used as the surface ligand in every QDs. Fluorescence measurements were made to detect the acceptor-donor and understand the energy transfer mechanism in the QD:BPB associate. It was observed that the quenching amount of QDs in the QD: BPB hybrid associate varied according to the QD type used, and the highest emission quenching was observed in the CdSeTe: BPB associate. In order to suppress charge recombination in designed QD:BPB hybrid QDSSCs, CdS QDs were coated on TiO2 surface with SILAR method and ZnS layer was coated to passivize the photoactive surface. In the study, it was determined that the QD:BPB hybrid associate increased the power conversation efficiency (PCE) of QDSCC among all three QDs tested, and this increase was found to be in the range of 9–12.5%. As a result, Jsc for TiO2/CdS/CdSeTe/BPB/ZnS QDSSCs was measured as 10.3 mA/cm2, Voc was 0.791 V, and it was calculated that PCE increased to 4.78 ± 0.1%. © 2021 Elsevier B.V.