Molecules (Mar 2013)

Synthesis and Antiviral Activity of N-Phenylbenzamide Derivatives, a Novel Class of Enterovirus 71 Inhibitors

  • Zhuo-Rong Li,
  • Yu-Huan Li,
  • Jian-Dong Jiang,
  • Yan-Ping Li,
  • Rong-Mei Gao,
  • Wei-Ying He,
  • Lan-Hu Hao,
  • Hui-Qiang Wang,
  • Xing-Yue Ji

DOI
https://doi.org/10.3390/molecules18033630
Journal volume & issue
Vol. 18, no. 3
pp. 3630 – 3640

Abstract

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A series of novel N-phenylbenzamide derivatives were synthesized and their anti-EV 71 activities were assayed in vitro. Among the compounds tested, 3-amino-N-(4-bromophenyl)-4-methoxybenzamide (1e) was active against the EV 71 strains tested at low micromolar concentrations, with IC50 values ranging from 5.7 ± 0.8–12 ± 1.2 μM, and its cytotoxicity to Vero cells (TC50 = 620 ± 0.0 μM) was far lower than that of pirodavir (TC50 = 31 ± 2.2 μM). Based on these results, compound 1e is a promising lead compound for the development of anti-EV 71 drugs.

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