Synthesis of 2-hydrazolyl-4-thiazolidinones based on multicomponent reactions and biological evaluation against Trypanosoma Cruzi

Chem Biol Drug Des. 2011 Mar;77(3):166-72. doi: 10.1111/j.1747-0285.2010.01071.x. Epub 2011 Jan 19.

Abstract

A series of 18 novel 2-hydrazolyl-4-thiazolidinones-5-carboxylic acids, amides and 5,6-α,β-unsaturated esters were synthesized, and their in vitro activity on cruzipain and T. cruzi epimastigotes was determined. Some agents show activity at 37 μm concentration in the enzyme assay. Computational tools and docking were used to correlate the biological response with the physicochemical parameters of the compounds and their cruzipain inhibitory effects.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetamides / chemical synthesis
  • Acetamides / chemistry
  • Acetamides / toxicity
  • Animals
  • Antiprotozoal Agents / chemical synthesis*
  • Antiprotozoal Agents / chemistry
  • Antiprotozoal Agents / toxicity
  • Binding Sites
  • Catalytic Domain
  • Chlorocebus aethiops
  • Computer Simulation
  • Cysteine Endopeptidases / chemistry
  • Cysteine Endopeptidases / metabolism
  • Protozoan Proteins
  • Quantitative Structure-Activity Relationship
  • Thiazolidines / chemistry*
  • Trypanosoma cruzi / drug effects*
  • Trypanosoma cruzi / enzymology
  • Vero Cells

Substances

  • Acetamides
  • Antiprotozoal Agents
  • Protozoan Proteins
  • Thiazolidines
  • acetamide
  • Cysteine Endopeptidases
  • cruzipain