SYNTHESIS AND CYTOTOXIC EVALUATION OF SOME 2-{4-[(2-OXO-1,2-DIHYDRO-3H-INDOL-3-YLIDENE)METHYL] PHENOXY}-N-PHENYLACETAMIDE

Acta Pol Pharm. 2017 Jan;74(1):137-145.

Abstract

A series of 2-oxindole derivatives were synthesized and evaluated for cytotoxic activity against different human and murine cancer cell lines and cancer chemopreventive activity. Among the tested compounds VS-06, 08, 12 and 17 displayed cytotoxic activity in the range of 5.0 to 8.5 pM against human T-lymphocyte cells (CEM). Results showed that molecules with electron withdrawing substituent at 4 position of N-phenylacetamide group exhibited an increase in activity against the human tumor cell line CEM. The cancer chemo- preventive effect of VS-01 (IC₅₀ = 451 nM) displayed equipotent activity in comparison to standard oleanolic acid (IC₅₀ = 449 nM).

MeSH terms

  • Animals
  • Anticarcinogenic Agents / chemical synthesis*
  • Anticarcinogenic Agents / pharmacology
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Humans
  • Structure-Activity Relationship

Substances

  • Anticarcinogenic Agents
  • Antineoplastic Agents