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Effect of catechol derivatives on cell growth and lipoxygenase activity

  • Julie Simpson
  • , Rebecca Forrester
  • , Michael J. Tisdale
  • , David C. Billington
  • , Daniel L. Rathbone*
  • *Corresponding author for this work
  • Aston University

Research output: Contribution to journalArticlepeer-review

Abstract

Derivatives of salicylic acid have been synthesized as potential lipoxygenase inhibitors. Agents containing a phenolic dihydroxy moiety showed potent (IC 5010 -6-10 -7 M) inhibition of the growth of murine colonic tumour cells in vitro, and were effective inhibitors of 5-, 12- and 15-lipoxygenase in intact cells. The catechols were also potent inhibitors of rabbit reticulocyte 15-lipoxygenase (IC 50 ∼1 μM). © 2003 Elsevier Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)2435-2439
Number of pages5
JournalBioorganic and Medicinal Chemistry Letters
Volume13
Issue number15
DOIs
Publication statusPublished - 4 Aug 2003

Keywords

  • salicylic acid
  • lipoxygenase inhibitors
  • phenolic dihydroxy moiety
  • murine colonic tumour cells
  • inhibitors
  • catechols

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