Literature DB >> 34173883

Insights on a new sulfonamide chalcone with potential antineoplastic application.

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

Mesh:

Substances:

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


  44 in total

1.  Antifungal chalcones from Maclura tinctoria.

Authors:  H N ElSohly; A S Joshi; A C Nimrod; L A Walker; A M Clark
Journal:  Planta Med       Date:  2001-02       Impact factor: 3.352

Review 2.  A review of anti-infective and anti-inflammatory chalcones.

Authors:  Zdzisława Nowakowska
Journal:  Eur J Med Chem       Date:  2006-11-15       Impact factor: 6.514

3.  Chalcone derivatives from the fern Cyclosorus parasiticus and their anti-proliferative activity.

Authors:  Han Wei; Xuenong Zhang; Guanghua Wu; Xian Yang; Songwei Pan; Yanyan Wang; Jinlan Ruan
Journal:  Food Chem Toxicol       Date:  2013-07-26       Impact factor: 6.023

4.  Anti-breast cancer activity of heteroaryl chalcone derivatives.

Authors:  V Raja Solomon; Hoyun Lee
Journal:  Biomed Pharmacother       Date:  2011-12-31       Impact factor: 6.529

5.  Anti-tumor effects by a synthetic chalcone compound is mediated by c-Myc-mediated reactive oxygen species production.

Authors:  Tae-Hee Kim; Woo Duck Seo; Hyung Won Ryu; Haeng Ran Seo; Yeung Bae Jin; Minyoung Lee; Young-Hoon Ji; Ki Hun Park; Yun-Sil Lee
Journal:  Chem Biol Interact       Date:  2010-07-08       Impact factor: 5.192

6.  Synthesis and anti-parasitic activity of a novel quinolinone-chalcone series.

Authors:  Marina Roussaki; Belinda Hall; Sofia Costa Lima; Anabela Cordeiro da Silva; Shane Wilkinson; Anastasia Detsi
Journal:  Bioorg Med Chem Lett       Date:  2013-09-25       Impact factor: 2.823

7.  β-Ionone derived chalcones as potent antiproliferative agents.

Authors:  Vishal Sharma; Ashun Chaudhary; Saroj Arora; Ajit K Saxena; Mohan Paul S Ishar
Journal:  Eur J Med Chem       Date:  2013-08-19       Impact factor: 6.514

8.  Novel 1-(7-ethoxy-1-benzofuran-2-yl) substituted chalcone derivatives: Synthesis, characterization and anticancer activity.

Authors:  Demet Coskun; Merve Erkisa; Engin Ulukaya; Mehmet Fatih Coskun; Ferda Ari
Journal:  Eur J Med Chem       Date:  2017-05-05       Impact factor: 6.514

9.  Synthesis of novel quinoline-2-one based chalcones of potential anti-tumor activity.

Authors:  Rodrigo Abonia; Daniel Insuasty; Juan Castillo; Braulio Insuasty; Jairo Quiroga; Manuel Nogueras; Justo Cobo
Journal:  Eur J Med Chem       Date:  2012-09-06       Impact factor: 6.514

10.  Inhibitory effect of naringenin chalcone on inflammatory changes in the interaction between adipocytes and macrophages.

Authors:  Shizuka Hirai; Young-Il Kim; Tsuyoshi Goto; Min-Sook Kang; Mineka Yoshimura; Akio Obata; Rina Yu; Teruo Kawada
Journal:  Life Sci       Date:  2007-09-12       Impact factor: 5.037

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