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The design, synthesis and activity of non-ATP competitive inhibitors of pp60c-src tyrosine kinase. Part 1: Hydroxynaphthalene derivatives

  • SUNY Buffalo
  • Scripps Research Institute

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

A series of hydroxynaphthalene pp60c-src non-peptide inhibitors was designed, using the crystal structure of the insulin receptor tyrosine kinase as a qualitative model, to target the peptide substrate binding site. Representative inhibitors were shown to bind non-competitively with respect to ATP.

Original languageEnglish
Pages (from-to)477-481
Number of pages5
JournalBioorganic and Medicinal Chemistry Letters
Volume10
Issue number5
DOIs
StatePublished - Mar 6 2000

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