Synthesis and photosensitizing efficacy of isomerically pure bacteriopurpurinimides

J Med Chem. 2004 Sep 23;47(20):4814-7. doi: 10.1021/jm049630s.

Abstract

The isomerically pure 3-deacetyl-3-(1-heptyloxy)ethylbacteriopurpurin-N-hexylimides exhibiting long-wavelength absorption near 800 nm were obtained from 3-acetylbacteriopurpurin-N-hexylimide in high stereospecificity by following Corey's synthetic approach. Both heptyl ether derivatives (R- and S-isomers) showed similar in vitro photosensitizing efficacy and limited skin phototoxicity and were found to localize in mitochondria. However, in preliminary in vivo screening, compared to the S-isomer, the corresponding R-isomer produced enhanced in vivo photodynamic therapy efficacy.

Publication types

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

MeSH terms

  • Animals
  • Biochemistry / methods
  • Chromatography, High Pressure Liquid / methods
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor / methods
  • Mice
  • Mice, Inbred C3H
  • Neoplasms, Experimental / drug therapy
  • Photochemotherapy / methods
  • Photosensitizing Agents / chemical synthesis
  • Photosensitizing Agents / chemistry*
  • Photosensitizing Agents / pharmacology*
  • Stereoisomerism
  • Structure-Activity Relationship
  • Tumor Cells, Cultured

Substances

  • Photosensitizing Agents