1. Academic Validation
  2. Characterization of two taxol photoaffinity analogues bearing azide and benzophenone-related photoreactive substituents in the A-ring side chain

Characterization of two taxol photoaffinity analogues bearing azide and benzophenone-related photoreactive substituents in the A-ring side chain

  • J Med Chem. 1994 May 13;37(10):1446-9. doi: 10.1021/jm00036a009.
C S Swindell 1 J M Heerding N E Krauss S B Horwitz S Rao I Ringel
Affiliations

Affiliation

  • 1 Department of Chemistry, Bryn Mawr College, Pennsylvania 19010.
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 beta-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.

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