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.

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Affinity Labels / chemical synthesis
  • Affinity Labels / metabolism
  • Affinity Labels / pharmacology*
  • Animals
  • Azides / chemical synthesis
  • Azides / metabolism
  • Azides / pharmacology*
  • CHO Cells
  • Cattle
  • Cell Division / drug effects
  • Cell Line
  • Cricetinae
  • Cricetulus
  • Mice
  • Microtubules / drug effects
  • Microtubules / metabolism
  • Paclitaxel / analogs & derivatives*
  • Paclitaxel / chemical synthesis
  • Paclitaxel / metabolism
  • Paclitaxel / pharmacology
  • Photochemistry
  • Taxoids*

Substances

  • Affinity Labels
  • Azides
  • Taxoids
  • 3'-(4-azidobenzamido)taxol
  • benzoyltaxol
  • Paclitaxel