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Discovery of Potent and Selective Halogen-Substituted Imidazole-Thiosemicarbazides for Inhibition of Toxoplasma gondii Growth In Vitro via Structure-Based Design.

Agata PanethLidia WęglińskaAdrian BekierEdyta StefaniszynMonika WujecNazar TrotskoAnna HawryłMiroslaw HawryłKatarzyna Dzitko
Published in: Molecules (Basel, Switzerland) (2019)
Employing a simple synthetic protocol, a series of highly effective halogen-substituted imidazole-thiosemicarbazides with anti-Toxoplasma gondii effects against the RH tachyzoites, much better than sulfadiazine, were obtained (IC50s 10.30-113.45 µg/mL vs. ~2721.45 µg/mL). The most potent of them, 12, 13, and 15, blocked the in vitro proliferation of T. gondii more potently than trimethoprim (IC50 12.13 µg/mL), as well. The results of lipophilicity studies collectively suggest that logP would be a rate-limiting factor for the anti-Toxoplasma activity of this class of compounds.
Keyphrases
  • toxoplasma gondii
  • molecular docking
  • randomized controlled trial
  • small molecule
  • anti inflammatory
  • signaling pathway
  • case control