Some novel 3-phenyl-2-[(E)-2-phenylethenyl]-3,4-dihydroquinazolin-4-one derivatives possessing para-sulfonamides groups on the phenyl ring of the 2-phenylethenyl moiety have been synthesized and their COX-2 inhibitory activity evaluated. The stuctures of the synthesized compounds were confirmed on the basis of FT-IR, 1H-NMR, 13C-NMR and mass spectral data. The COX-2 inhibition screening assay revealed that 4-[(E)-2-{3-(4-methoxyphenyl)-4-oxo-3,4-dihydroquinazolin-2-yl}ethenyl]benzene-l-sulfonamide had a maximum COX-2 inhibition (47.1%), at a concentration of 20 μM. © 2012 by the authors; licensee MDPI, Basel, Switzerland.
CITATION STYLE
Hayun, Hudiyono, S., Hanafi, M., & Yanuar, A. (2012). Synthesis and COX-2 inhibitory activity of 4-[(,E)-2-(4-Oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)ethenyl]benzene-l-sulfonamide and its analogs. Pharmaceuticals, 5(12), 1282–1290. https://doi.org/10.3390/ph5121282
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