Synthesis and evaluation of antitumoral activity of ester and amide derivatives of 2-arylamino-6-trifluoromethyl-3-pyridinecarboxylic acids

Bioorg Med Chem. 2008 Mar 1;16(5):2367-78. doi: 10.1016/j.bmc.2007.11.069. Epub 2007 Nov 29.

Abstract

The synthesis and antitumoral activity of ester and amide derivatives of 2-arylamino-6-trifluoromethyl-3-pyridinecarboxylic acids 8-58 is described. Trifluoromethylpyridine derivatives 8-58 were evaluated for their anticancer activity toward human tumoral cell lines by the National Cancer Institute (NCI). Most of them possess encouraging anticancer activity, having GI(50) values in the low micromolar to nanomolar concentration range. The 3,4,5-trimethoxyphenylamide 44 was the most active, and it is now under review by NCI Biological Evaluation Committee for possible further studies.

MeSH terms

  • Amides / chemical synthesis*
  • Amides / chemistry
  • Amides / pharmacology*
  • Amination
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Esters / chemical synthesis*
  • Esters / chemistry
  • Esters / pharmacology*
  • Fluorine Compounds / chemistry
  • Humans
  • Methylation
  • Molecular Structure
  • Niacin / chemistry*
  • Sensitivity and Specificity
  • Structure-Activity Relationship

Substances

  • Amides
  • Antineoplastic Agents
  • Esters
  • Fluorine Compounds
  • Niacin