Purpurinimides as photosensitizers: effect of the presence and position of the substituents in the in vivo photodynamic efficacy

Bioorg Med Chem Lett. 2000 Jul 3;10(13):1463-6. doi: 10.1016/s0960-894x(00)00274-2.

Abstract

This study presents a novel approach for the regioselective synthesis of a series of alkyl ether analogues of purpurin-18-N-alkylimide. In the purpurinimide series, this is the first example which demonstrates that the presence and position of the substituents in the macrocycle makes a remarkable difference in the in vivo PDT efficacy.

Publication types

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

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / therapeutic use
  • Cyanobacteria / chemistry
  • Drug Design
  • Drug Screening Assays, Antitumor
  • Magnetic Resonance Spectroscopy
  • Mice
  • Molecular Structure
  • Neoplasm Transplantation
  • Neoplasms, Experimental / drug therapy*
  • Neoplasms, Experimental / metabolism
  • Photochemotherapy*
  • Photosensitizing Agents / chemistry*
  • Photosensitizing Agents / pharmacokinetics
  • Photosensitizing Agents / therapeutic use*
  • Porphyrins / chemical synthesis*
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Photosensitizing Agents
  • Porphyrins