398514-79-9Relevant academic research and scientific papers
Water soluble, core-modified porphyrins. 3. Synthesis, photophysical properties, and in vitro studies of photosensitization, uptake, and localization with carboxylic acid-substituted derivatives
You, Youngjae,Gibson, Scott L.,Hilf, Russell,Davies, Sherry R.,Oseroff, Allan R.,Roy, Indrajit,Ohulchanskyy, Tymish Y.,Bergey, Earl J.,Detty, Michael R.
, p. 3734 - 3747 (2007/10/03)
Water soluble, core-modified porphyrins 1-5 bearing 1-4 carboxylic acid groups were prepared and evaluated in vitro as photosensitizers for photodynamic therapy. The 21,23-core-modified porphyrins 1-5 gave band I absorption maxima with λmax of
Water-soluble, core-modified porphyrins as novel, longer-wavelength-absorbing sensitizers for photodynamic therapy. II. Effects of core heteroatoms and meso-substituents on biological activity
Hilmey, David G.,Abe, Masako,Nelen, Marina I.,Stilts, Corey E.,Baker, Gary A.,Baker, Sheila N.,Bright, Frank V.,Davies, Sherry R.,Gollnick, Sandra O.,Oseroff, Allan R.,Gibson, Scott L.,Hilf, Russell,Detty, Michael R.
, p. 449 - 461 (2007/10/03)
Water-soluble, core-modified porphyrins were prepared and evaluated as sensitizers for photodynamic therapy (PDT). The addition of an aromatic aldehyde to 2,5-dilithiothiophene or -selenophene gave diol 3 as a nearly equimolar mixture of meso and d,1 dias
