High yield preparation of purpurin-18 from Spirulina maxima

[1]  A. Oseroff,et al.  Compared to purpurinimides, the pyropheophorbide containing an iodobenzyl group showed enhanced PDT efficacy and tumor imaging (124I-PET) ability. , 2009, Bioconjugate chemistry.

[2]  Lalit N. Goswami,et al.  Characterization of porphyrins, chlorins, and bacteriochlorins formed via allomerization of bacteriochlorophyll a. Synthesis of highly stable bacteriopurpurinimides and their metal complexes. , 2006, The Journal of organic chemistry.

[3]  S. Bhattacharya,et al.  Evaluation of three Spirulina species grown under similar conditions for their growth and biochemicals , 2005 .

[4]  Roger Guilard,et al.  The porphyrin handbook , 2002 .

[5]  T. Dougherty,et al.  Synthesis, photophysical properties, tumor uptake, and preliminary in vivo photosensitizing efficacy of a homologous series of 3-(1'-alkyloxy)ethyl-3-devinylpurpurin-18-N-alkylimides with variable lipophilicity. , 2001, Journal of medicinal chemistry.

[6]  T. Dougherty,et al.  Photosensitizers related to purpurin-18-N-alkylimides: a comparative in vivo tumoricidal ability of ester versus amide functionalities. , 2000, Bioorganic & medicinal chemistry letters.

[7]  E. W. Baker,et al.  Chlorophyll-a degradation during cellular senescence and death , 1998 .

[8]  Annabeth L. Propst,et al.  Designing for Quality: An introduction to the best of Taguchi and Western methods of statistical experimental design , 1990 .

[9]  Nobuto Yamamoto,et al.  PHOTODYNAMIC SENSITIZERS FROM CHLOROPHYLL:PURPURIN–18 AND CHLORINp6 , 1988, Photochemistry and photobiology.