Synthesis, anti-proliferative and genotoxicity studies of 6-chloro-5-(2-substituted-ethyl)-1,3-dihydro-2H-indol-2-ones and 6-chloro-5-(2-chloroethyl)-3-(alkyl/ary-2-ylidene)indolin-2-ones

Eur J Med Chem. 2016 Oct 4:121:221-231. doi: 10.1016/j.ejmech.2016.05.028. Epub 2016 May 13.

Abstract

A series of 6-chloro-5-(2-substituted-ethyl)-1,3-dihydro-2H-indol-2-ones (3a-h) and 6-chloro-5-(2-chloroethyl)-3-(alkyl/aryl-2-ylidene)indolin-2-ones (5i-x) were synthesized. Compounds 3a-e, 5i-l and 5q-r were selected by NIH, USA for in vitro anti-proliferative screening. Based on the impressive growth inhibitory (GI %) effect by the compounds 3a-b and 3e which showed growth inhibition in the range 1.22-76.30%, 2.85-76.03% and 10.98-82.05% respectively at 10(-5) concentration, these compounds were further analyzed for anti-proliferative activity at 5 dose concentration and genotoxicity.

Keywords: 2H-Indol-2-ones; Anti-proliferative activity; Cell line; Genotoxicity.

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Dose-Response Relationship, Drug
  • Humans
  • Indoles / chemistry*
  • Indoles / pharmacology
  • Mutagens / chemistry
  • Mutagens / pharmacology

Substances

  • Antineoplastic Agents
  • Indoles
  • Mutagens
  • indolin-2-one