
2-Phenyl-6,7-difluoro and 2-(4-fluorophenyl)quinazoline derivatives bearing salicylidenhydrazino fragments at position 4 were prepared based on 4,5-difluoroantranilic acid or anthranilamide. Molecular docking to casein kinase 2 was performed; compounds with high in silico activity to CK2 were revealed. Cytotoxic activity of the synthesized compounds was studied on cancer cell line MDA-MB-231 and normal cell line WI26 VA4.
SALICYLIDENHYDRAZINES, 2-arylquinazolines, salicylidenhydrazines, in silico activity, CYTOTOXIC ACTIVITY, 2-ARYLQUINAZOLINES, Chemistry, CASEIN KINASE 2 INHIBITOR, IN SILICO ACTIVITY, casein kinase 2 inhibitor, QD1-999, cytotoxic activity
SALICYLIDENHYDRAZINES, 2-arylquinazolines, salicylidenhydrazines, in silico activity, CYTOTOXIC ACTIVITY, 2-ARYLQUINAZOLINES, Chemistry, CASEIN KINASE 2 INHIBITOR, IN SILICO ACTIVITY, casein kinase 2 inhibitor, QD1-999, cytotoxic activity
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