Structural determinants of putrescine uptake inhibition produced by cationic diamidines in the model of trypanosomatid Crithidia fasciculata

Biol Chem. 1996 Dec;377(12):833-6. doi: 10.1515/bchm3.1996.377.12.833.

Abstract

The effect of a heterologous series of cationic diamidines has been tested on cell growth and polyamine uptake on the model of insect Trypanosomatid Crithidia fasciculata. The maximum inhibitory effect on both parameters was found for pentamidine and dibromopropamidine, which exhibit a longer distance between amino and imino substituents. A minimum inhibitory effect was found with amicarbalide. A good relationship was obtained when the distance between amino moieties was plotted versus the inhibitory effect on putrescine uptake, suggesting a role of this structural property on polyamine transport in Crithidia fasciculata. In addition, a similar correlation was obtained for another Trypanosomatid parasite, Leishmania infantum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzamidines / chemistry
  • Benzamidines / pharmacology*
  • Carbanilides / pharmacology
  • Crithidia / drug effects
  • Crithidia / growth & development*
  • Indoles / pharmacology
  • Leishmania
  • Pentamidine / pharmacology
  • Putrescine / pharmacokinetics*
  • Stilbamidines / pharmacology
  • Structure-Activity Relationship
  • Trypanocidal Agents / pharmacology*

Substances

  • Benzamidines
  • Carbanilides
  • Indoles
  • Stilbamidines
  • Trypanocidal Agents
  • phenamidine
  • hydroxystilbamidine
  • DAPI
  • Pentamidine
  • amicarbalide diisethionate
  • propamidine
  • stilbamidine
  • Putrescine