Anti-protozoal activity of diamine derivatives

Biomed Pharmacother. 2011 Feb;65(1):60-2. doi: 10.1016/j.biopha.2010.10.006. Epub 2010 Nov 4.

Abstract

Ten N-monoalkylated diamines were synthesized and evaluated for in vitro activities against Trichomonas vaginalis and Giardia lamblia. Several compounds displayed a good inhibition of parasite growth, with MIC less or equal to 20μg/mL. N-hexadecil-1,4-butanediamine was found to be the most active compound in vitro against T. vaginalis with MIC of 2.5μg/mL, twice more active in comparison to the reference drug metronidazole (MTZ). Seven of the studied compounds showed a better anti-G. lamblia activity than MTZ.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiprotozoal Agents / pharmacology*
  • Diamines / pharmacology*
  • Giardia lamblia / drug effects
  • Structure-Activity Relationship
  • Trichomonas vaginalis / drug effects

Substances

  • Antiprotozoal Agents
  • Diamines