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Bioorg Khim ; 29(2): 214-21, 2003.
Artículo en Ruso | MEDLINE | ID: mdl-12708323

RESUMEN

New derivatives of bacteriochlorophyll a bearing an extra glutarimide exocycle were synthesized, and their reactivity was studied. Acetyl group in 3-acetyl-2,7,12,18-tetramethyl-8-ethyl-13,15- dicarboxy-17-carboxyethyl-7,8,17,18-tetrahydroporphyrin (bacteriochlorin p) was chemically modified into alpha-hydroxyethyl and vinyl groups. A simple method of preparation of vinylbacteriopurpurin esters under the catalysis by p-toluenesulfonic acid was proposed. The resulting compounds exhibit a high adsorption in the visible and near IR areas of electronic spectra, a reasonable stability, and amphiphilic properties and, therefore, may be regarded as promising photosensitizers for the photodynamic cancer therapy.


Asunto(s)
Fármacos Fotosensibilizantes/química , Porfirinas/química , Bacterioclorofila A/química , Bioquímica/métodos , Espectroscopía de Resonancia Magnética , Estructura Molecular , Neoplasias/terapia , Fármacos Fotosensibilizantes/síntesis química , Fármacos Fotosensibilizantes/farmacología , Espectrofotometría Infrarroja
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