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Privileged scaffolds for blocking protein-protein interactions: 1,4-Disubstituted naphthalene antagonists of transcription factor complex HOX-PBX/DNA

  • SUNY Buffalo
  • Roswell Park Cancer Institute

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Structure-based-design studies, with the crystal structure of the HOXB1-PBX1/DNA transcription factor complex, were used to identify 1,4-disubstituted naphthalenes as potential antagonists. An initial library of 32 analogs was synthesized, two of which were found to be more potent than the reported activity for a 12 amino acid peptide antagonist. Antagonists were also identified of the related BRN1/DNA and BRN2/DNA transcription factor complexes indicating that a 1,4-disubsituted naphthalene may be a privileged scaffold for preparing screening libraries targeting this family of transcription factor complexes.

Original languageEnglish
Pages (from-to)3875-3879
Number of pages5
JournalBioorganic and Medicinal Chemistry Letters
Volume14
Issue number15
DOIs
StatePublished - Aug 2 2004

Keywords

  • BRN
  • HOX
  • PBX
  • Protein-protein interaction antagonists
  • Transcription factor complex antagonists

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