Synthesis and in vitro Cytotoxicity of 1-Benzoyl-3-methyl Thiourea Derivatives

Add time:07/17/2019    Source:sciencedirect.com

Thioureas are important sulfur and nitrogen containing compounds and they are useful substances in drug research. In an effort to improve potential anticancer activities, two novel 1-benzoyl-3-methyl thiourea derivatives were designed and synthesized with substitution at aromatic positions of C-3, and C-4 of 1-benzoyl-3-methyl thiourea. Their structures were confirmed using IR, MS and 1H-NMR. The in vitro cytotoxicity against HeLa cell lines were evaluated by the standard MTT assay. All of the compounds exhibited more potent cytotoxicity with IC50 values of 160–383 μg/mL stronger than hydroxyurea with IC50 value of 428 μg/mL.

We also recommend Trading Suppliers and Manufacturers of methyl 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetate (cas 1601-18-9). Pls Click Website Link as below: cas 1601-18-9 suppliers

Prev:Ligand photolysis and recombination of Fe(II)protoporphyrin IX complexes in Tetramethylene sulfoxide (cas 1600-44-8)
Next:Behavioral and electrophysiological analyses of the effects of 2-o-chlorobenzoyl-4- chloro-n-methyl-nα-glycylglycinanilide hydrate (45-0088-s) in the cns in cats and monkeys)