Synthesis and antitumor evaluation of a novel series of triaminotriazine derivatives

Bioorg Med Chem. 2007 Feb 15;15(4):1815-27. doi: 10.1016/j.bmc.2006.11.028. Epub 2006 Nov 19.

Abstract

A series of triaminotriazine derivatives (compounds 5a-f, 6a-x, and 7a-g) was designed, synthesized, and evaluated for their inhibition activities to colorectal cancer (CRC) cell lines (HCT-116 and HT-29). Most of the synthesized compounds demonstrated moderate anti-proliferatory effects on both HCT-116 and HT-29 cell lines at the concentration of 10 microM. The inhibitory activities against HCT-116 and HT-29 cell lines were discussed to develop the structure-activity relationships of this new series. Compounds 6l and 6o exhibited prominent inhibition activities toward HCT-116, with IC50s of 0.76 and 0.92 microM, respectively. The in vivo antitumor studies and pharmacokinetics of compound 6l showed that it might be a promising new hit for further development of antitumor agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / pathology
  • Drug Design
  • Drug Screening Assays, Antitumor
  • Humans
  • Inhibitory Concentration 50
  • Structure-Activity Relationship
  • Triazines / chemical synthesis*
  • Triazines / pharmacology*

Substances

  • Antineoplastic Agents
  • Triazines