Synthesis of 1-(2-chloro-2-phenylethyl)-6-methylthio-1H-pyrazolo[3,4-d]pyrimidines 4-amino substituted and their biological evaluation

Eur J Med Chem. 2004 Feb;39(2):153-60. doi: 10.1016/j.ejmech.2003.11.007.

Abstract

A new series of 4-amino-6-methylthio-1H-pyrazolo[3,4-d]pyrimidines (2a-m) bearing the 2-chloro-2-phenylethyl chain at the N1 position, has been synthesized. The affinity of these compounds for A1 adenosine receptor (A1AR) was measured. The compounds showed poor affinity. A more interesting result was obtained by 2a, 2d, 2g, which demonstrated inhibitory activity on cell proliferation of the A-431 cell line stimulated by epithelial growth factor (EGF) and on EGF receptor tyrosine kinase (EGFR-TK) phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine A1 Receptor Antagonists
  • Cell Division / drug effects
  • Cell Line, Tumor
  • Drug Screening Assays, Antitumor / methods
  • Epidermal Growth Factor / antagonists & inhibitors
  • Epidermal Growth Factor / pharmacology
  • ErbB Receptors / antagonists & inhibitors
  • Humans
  • Molecular Structure
  • Phosphorylation
  • Pyrimidines / chemical synthesis*
  • Pyrimidines / pharmacology*
  • Receptor, Adenosine A1 / metabolism

Substances

  • Adenosine A1 Receptor Antagonists
  • Pyrimidines
  • Receptor, Adenosine A1
  • Epidermal Growth Factor
  • ErbB Receptors