New bis 4-bromobenzene sulphonate compound: Synthesis, characterizaton, DFT study, antibacterial and leishmanicidal activity


Süleymanoğlu N., Af C., Direkel Ş., Çelik F., Güler H. İ.

JOURNAL OF THE INDIAN CHEMICAL SOCIETY, vol.101, no.12, 2024 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 101 Issue: 12
  • Publication Date: 2024
  • Doi Number: 10.1016/j.jics.2024.101490
  • Journal Name: JOURNAL OF THE INDIAN CHEMICAL SOCIETY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Analytical Abstracts, Chemical Abstracts Core
  • Karadeniz Technical University Affiliated: Yes

Abstract

The new bis 4-bromobenzene sulphonate compound called as ((1E,1 ' E)-(1,4-phenylenebis(azanylylidene))bis (methanylylidene))bis(4,1-phenylene) bis(4-bromobenzenesulfonate) (I) was synthesized. Fourier transform infrared (FTIR), proton and carbon-13 nuclear magnetic resonance (1H and 13 C NMR) methods were used to confirm the molecular structure. All calculations were performed at DFT/B3LYP/6-311G(d,p) level. IR and NMR spectral data were compared with experimental ones and the details of molecular structure were investigated. The antimicrobial activity of the synthesized compound (I) was determined by Alamar blue microdilution method against seven different established standard bacteria and one parasite isolate. The compound I exhibited antibacterial activity at different concentrations. Compound I was found to have antimicrobial activity on all bacterial species and L. infantum parasite, albeit at different concentrations. Compound I has the most effective antibacterial activity on S. flexneri and the least effect on S. aureus and E. cloacea bacteria. In order for the synthesized compound to be used as a drug candidate, in vivo control studies in a series of experimental animal models and whether it has toxic effects on human cells should be tested. In silico analysis was conducted on four different proteins using the synthesized compound Ito investigate the essential interactions responsible for its antibacterial activity. The docking results of compound I supported its antibacterial activity, revealing high inhibition constants.