Molecules (Sep 2020)

Biological Activities and ADMET-Related Properties of Novel Set of Cinnamanilides

  • Jiri Kos,
  • Andrzej Bak,
  • Violetta Kozik,
  • Timotej Jankech,
  • Tomas Strharsky,
  • Aleksandra Swietlicka,
  • Hana Michnova,
  • Jan Hosek,
  • Adam Smolinski,
  • Michal Oravec,
  • Ferdinand Devinsky,
  • Milan Hutta,
  • Josef Jampilek

DOI
https://doi.org/10.3390/molecules25184121
Journal volume & issue
Vol. 25, no. 18
p. 4121

Abstract

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A series of nineteen novel ring-substituted N-arylcinnamanilides was synthesized and characterized. All investigated compounds were tested against Staphylococcus aureus as the reference strain, two clinical isolates of methicillin-resistant S. aureus (MRSA), and Mycobacterium tuberculosis. (2E)-N-[3-Fluoro-4-(trifluoromethyl)phenyl]-3-phenylprop-2-enamide showed even better activity (minimum inhibitory concentration (MIC) 25.9 and 12.9 µM) against MRSA isolates than the commonly used ampicillin (MIC 45.8 µM). The screening of the cell viability was performed using THP1-Blue™ NF-κB cells and, except for (2E)-N-(4-bromo-3-chlorophenyl)-3-phenylprop-2-enamide (IC50 6.5 µM), none of the discussed compounds showed any significant cytotoxic effect up to 20 μM. Moreover, all compounds were tested for their anti-inflammatory potential; several compounds attenuated the lipopolysaccharide-induced NF-κB activation and were more potent than the parental cinnamic acid. The lipophilicity values were specified experimentally as well. In addition, in silico approximation of the lipophilicity values was performed employing a set of free/commercial clogP estimators, corrected afterwards by the corresponding pKa calculated at physiological pH and subsequently cross-compared with the experimental parameters. The similarity-driven property space evaluation of structural analogs was carried out using the principal component analysis, Tanimoto metrics, and Kohonen mapping.

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