Research on Chemical Intermediates

, Volume 38, Issue 2, pp 559–569

Cytotoxicity, antioxidant, and antimicrobial activities of novel 2-quinolone derivatives derived from coumarin

Authors

    • Biotechnology Division, Applied Science DepartmentUniversity of Technology
    • Department of Chemical and Processing Engineering, Faculty of Engineering and Built EnvironmentUniversiti of Kebangsaan Malaysia
  • Redha I. H. Al-Bayati
    • Department of ChemistryCollege of Sciences, Al-Mustansiriyah University
  • Kawkab Y. Saour
    • Department of PharmacologyCollege of Pharmacy, Baghdad University
  • Mahdi F. Radi
    • Department of ChemistryCollege of Sciences, Al-Mustansiriyah University
Article

DOI: 10.1007/s11164-011-0371-2

Cite this article as:
Al-Amiery, A.A., Al-Bayati, R.I.H., Saour, K.Y. et al. Res Chem Intermed (2012) 38: 559. doi:10.1007/s11164-011-0371-2

Abstract

Coumarins are important and useful compounds with diverse pharmacological properties. New coumarin derivatives namely N-aminoquinoline-2-one 1, 1-((4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)methyleneamino)quinolin-2(1H)-one 2 and 1,1′-(1E,1′E)-(1,4-phenylenebis(methan-1-yl-1-ylidene))bis(azan-1-yl-1-ylidene)diquinolin-2(1H)-one 3, were synthesized and characterized by UV–Vis, FT-IR, and NMR spectra in addition of elemental analysis. The synthesized compounds (2 and 3) show considerable anticancer activity against HEp-2 cell line. Synthesized compounds (2 and 3) were tested against selected types of microbial organisms and showed significant activities. The free-radical scavenging activity of synthesized compounds (2 and 3) have been determined by their interaction with the stable free-radical 1,1-diphenyl-2-picrilhydrazyl (DPPH) and all the compounds have shown encouraging antioxidant activities.

Keywords

AnticancerAntioxidantAntimicrobialHEp-2 cell lineQuinolone

Copyright information

© Springer Science+Business Media B.V. 2011