Benzotriazole-oxadiazole hybrid compounds: Synthesis, anticancer activity, molecular docking and ADME profiling studies
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Erişim
info:eu-repo/semantics/embargoedAccessTarih
2022Yazar
Mermer, ArifBülbül, Muhammet Volkan
Kalender, Semiha Mervenur
Keskin, İlknur
Tüzün, Burak
Eyüpoğlu, Ozan Emre
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Tüm öğe kaydını gösterKünye
Mermer, A., Bülbül, M. V., Kalender, S. M., Keskin, İ., Tüzün, B. ve Eyüpoğlu, O. E. (2022). Benzotriazole-oxadiazole hybrid compounds: Synthesis, anticancer activity, molecular docking and ADME profiling studies. Journal of Molecular Liquids, 359. https://doi.org/10.1016/j.molliq.2022.119264Özet
Herein the designed novel benzotriazole-oxadiazole hybrid compounds were synthesized using both conventional method and ultrasound sonication (US) as an environmentally friendly method. It was observed that the US method provided an increase in reaction yields by reducing the reaction time approximately 3-fold. The synthesized compounds were investigated against PANC-1 cell line. All obtained compounds were characterized by FT-IR, 1H NMR, 13C NMR and MS spectroscopic techniques. The compounds 4b and 4d exhibited very promising anticancer activity results with IC50 values of 117.5 ± 0.084 μM and 87.82 ± 4.319 μM, respectively. Further, molecular docking studies to suggest how the synthesized compounds interact with the kinase domain of human DDR1 in complex of pancreatic Cancer proteins (PDB ID: 6HP9), and the crystal structure of PDEd of pancreatic Cancer proteins (PDB ID: 5E80). It was concluded from the docking studies that the compound 4d demonstrated the highest binding score values for active site of both proteins. Afterwards, ADME calculations were performed to examine the drug properties of benzotriazole-oxadiazole hybrid compounds.
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Q1Kaynak
Journal of Molecular LiquidsCilt
359Bağlantı
https://doi.org/10.1016/j.molliq.2022.1192640167-7322
https://hdl.handle.net/20.500.12511/9454
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