Synthesis, Anticancer Activities and Molecular Docking Studies of a Novel Class of 2-Phenyl-5,6,7,8-tetrahydroimidazo [1,2- b ]pyridazine Derivatives Bearing Sulfonamides.
Otmane BourzikatAbdelmoula El AbbouchiHamza GhammazNabil El BrahmiElmostfa El FahimeArnaud ParisRichard DaniellouFranck SuzenetGérald GuillaumetSaïd El KazzouliPublished in: Molecules (Basel, Switzerland) (2022)
In the present study, new 2-phenyl-5,6,7,8-tetrahydroimidazo [1,2- b ]pyridazines bearing sulfonamides were synthesized, characterized and evaluated for their anticancer activities. The structures of these derivatives were elucidated by 1 H NMR, 13 C NMR, infrared and high-resolution mass spectrometry for further validation of the target compound structures. The anticancer activities of the new molecules were evaluated against five human cancer cell lines, including A-549, Hs-683, MCF-7, SK-MEL-28 and B16-F10 cell lines using 5-fluorouracil and etoposide as the reference drugs. Among the tested compounds, 4e and 4f exhibited excellent activities in the same range of the positive controls, 5-fluorouracil and etoposide, against MCF-7 and SK-MEL-28 cancer cell lines, with IC 50 values ranging from 1 to 10 μM. The molecular docking studies of 4e and 4f showed a strong binding with some kinases, which are linked to MCF-7 and SK-MEL-28 cancer cell lines.