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Characterization of Two Taxol Photoaffinity Analogues Bearing Azide and Benzophenone-Related Photoreactive Substituents in the A-Ring Side Chain

  • Charles S. Swindell*
  • , Julia M. Heerding
  • , Nancy E. Krauss
  • , Susan Band Horwitz
  • , Srinivasa Rao
  • , Israel Ringel
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

Taxol is a structurally novel and clinically effective antitumor drug, which, unlike other antimitotic agents, induces the assembly of tubulin into microtubules. To characterize the binding site(s) of taxol on the microtubule, taxol-based photoaffinity reagents 1 and 2 bearing photoreactive groups on the A-ring side chain were prepared and evaluated. Taxol analogue 1 exhibits better microtubule assembly activity, greater cytotoxicity toward J774.2 cells, and more specific and efficient photolabeling of the β-subunit of tubulin than does analogue 2. Therefore, it would appear that 1 is the better candidate for further studies aimed at the characterization of the taxol binding site on the microtubule.

Original languageEnglish
Pages (from-to)1446-1449
Number of pages4
JournalJournal of Medicinal Chemistry
Volume37
Issue number10
DOIs
StatePublished - 1 May 1994

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