2,4-Diamino-quinazolines as inhibitors of beta-catenin/Tcf-4 pathway: Potential treatment for colorectal cancer

Bioorg Med Chem Lett. 2009 Sep 1;19(17):4980-3. doi: 10.1016/j.bmcl.2009.07.070. Epub 2009 Jul 17.

Abstract

The synthesis and SAR of a series of 2,4-diamino-quinazoline derivatives as beta-catenin/Tcf-4 inhibitors are described. This series was developed by modifying the initial lead 1, which was identified by screening of our compound library and found to inhibit the beta-catenin/Tcf-4 pathway. Replacement of the biphenyl moiety in compound 1 with the N-phenylpiperidine-4-carboxamide chain as in 2, resulted in a number of new analogues, which are potent inhibitors of the beta-catenin/Tcf-4 pathway. Compound such as 16k exhibited good cellular potency, solubility, metabolic stability and oral bioavailability.

MeSH terms

  • Anilides / chemical synthesis
  • Anilides / chemistry*
  • Anilides / pharmacokinetics
  • Animals
  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacokinetics
  • Cell Line, Tumor
  • Colorectal Neoplasms / drug therapy*
  • Female
  • Humans
  • Mice
  • Mice, Nude
  • Quinazolines / chemical synthesis
  • Quinazolines / chemistry*
  • Quinazolines / pharmacokinetics
  • Structure-Activity Relationship
  • TCF Transcription Factors / antagonists & inhibitors*
  • TCF Transcription Factors / metabolism
  • Wnt Proteins / antagonists & inhibitors
  • Wnt Proteins / metabolism
  • Xenograft Model Antitumor Assays
  • beta Catenin / antagonists & inhibitors*
  • beta Catenin / metabolism

Substances

  • Anilides
  • Antineoplastic Agents
  • Quinazolines
  • TCF Transcription Factors
  • Wnt Proteins
  • beta Catenin