| Literature DB >> 34173883 |
Patricia R S Wenceslau1, Renata L G de Paula1, Vitor S Duarte1, Giulio D C D'Oliveira2, Laura M M Guimarães1, Caridad N Pérez2, Leonardo L Borges1,3, José L R Martins4, James O Fajemiroye4,5, Chris H J Franco6, Pal Perjesi4,7, Hamilton B Napolitano8,9.
Abstract
Chalcones (E)-1,3-diphenyl-2-propene-1-ones, a class of biosynthetic precursor molecules of flavonoids, have a wide variety of biological applications. Besides the natural products, many synthetic derivatives and analogs became an object of continued interest in academia and industry. In this work, a synthesis and an extensive structural study were performed on a sulfonamide chalcone 1-Benzenesulfonyl-3-(4-bromobenzylidene)-2-(2-chlorophenyl)-2,3-dihydro-1H-quinolin-4-one with potential antineoplastic application. In addition, in silico experiments have shown that the sulfonamide chalcone fits well in the ligand-binding site of EGFR with seven μ-alkyl binding energy interactions on the ligand-binding site. Finally, the kinetic stability and the pharmacophoric analysis for EGFR indicated the necessary spatial characteristics for potential activity of sulfonamide chalcone as an antagonist.Entities:
Keywords: In silico experiments; M06-2X/6–311++G(d,p); Sulfonamide chalcone; X-ray diffraction
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Year: 2021 PMID: 34173883 DOI: 10.1007/s00894-021-04818-w
Source DB: PubMed Journal: J Mol Model ISSN: 0948-5023 Impact factor: 1.810