Incorporation of water-solubilizing groups in pyrazolopyrimidine mTOR inhibitors: discovery of highly potent and selective analogs with improved human microsomal stability. Academic Article uri icon

Overview

abstract

  • A series of highly potent and selective pyrazolopyrimidine mTOR inhibitors which contain water-solubilizing groups attached to the 6-arylureidophenyl moiety have been prepared. Such derivatives displayed superior potency to those in which these appendages were attached to alternative sites. In comparison to unfunctionalized arylureido compounds, these analogs demonstrated enhanced cellular potency and significantly improved stability towards human microsomes, resulting in an mTOR inhibitor with impressive efficacy in a xenograft model with an intermittent dosing regimen.

publication date

  • October 25, 2009

Research

keywords

  • Antineoplastic Agents
  • Intracellular Signaling Peptides and Proteins
  • Microsomes, Liver
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Kinase Inhibitors
  • Protein Serine-Threonine Kinases
  • Protein-Serine-Threonine Kinases
  • Pyrazoles
  • Pyrimidines

Identity

Scopus Document Identifier

  • 71849089048

Digital Object Identifier (DOI)

  • 10.1016/j.bmcl.2009.10.096

PubMed ID

  • 19896845

Additional Document Info

volume

  • 19

issue

  • 24