Molecules (Aug 2021)

Synthesis, In Silico and In Vitro Evaluation of Antimicrobial and Toxicity Features of New 4-[(4-Chlorophenyl)sulfonyl]benzoic Acid Derivatives

  • Theodora-Venera Apostol,
  • Mariana Carmen Chifiriuc,
  • Constantin Draghici,
  • Laura-Ileana Socea,
  • Luminita Gabriela Marutescu,
  • Octavian Tudorel Olaru,
  • George Mihai Nitulescu,
  • Elena Mihaela Pahontu,
  • Gabriel Saramet,
  • Stefania-Felicia Barbuceanu

DOI
https://doi.org/10.3390/molecules26165107
Journal volume & issue
Vol. 26, no. 16
p. 5107

Abstract

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The multi-step synthesis, physico-chemical characterization, and biological activity of novel valine-derived compounds, i.e., N-acyl-α-amino acids, 1,3-oxazol-5(4H)-ones, N-acyl-α-amino ketones, and 1,3-oxazoles derivatives, bearing a 4-[(4-chlorophenyl)sulfonyl]phenyl moiety are reported here. The structures of the newly synthesized compounds were confirmed by spectral (UV-Vis, FT-IR, MS, 1H- and 13C-NMR) data and elemental analysis results, and their purity was determined by RP-HPLC. The new compounds were assessed for their antimicrobial activity and toxicity to aquatic crustacean Daphnia magna. Also, in silico studies regarding their potential mechanism of action and toxicity were performed. The antimicrobial evaluation revealed that the 2-{4-[(4-chlorophenyl)sulfonyl]benzamido}-3-methylbutanoic acid and the corresponding 1,3-oxazol-5(4H)-one exhibited antimicrobial activity against Gram-positive bacterial strains and the new 1,3-oxazole containing a phenyl group at 5-position against the C. albicans strain.

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