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Benzoporphyrin Derivatives BPD

Benzoporphyrin derivatives were first synthesized by Callot et by reacting protoporphyrin IX with strongly [Pg.170]

Richter AM, Waterfield E, Jain AK, et al. Photosensitising potency of structural analogues of benzoporphyrin derivative (BPD) in a mouse tumour model. Br J Cancer 1991 63 87-93. [Pg.139]

N-methyl-4-pyridinium)-porphyrinato zine (II) triehloride 5-[4-Azidophenyl]-10,15,20-tri-(JV-methyl-4-pyridinium)porphyr-inato zinc (II) trichloride Benzoporphyrin derivative (BPD) 8.0... [Pg.246]

Benzoporphyrin derivative, monoacid, ring A adduct BPD, VERTEPORFIN, VISUDYNE... [Pg.954]

Fig. 2 Examples of photosensitizers presently approved for clinical applications or in clinical studies. mTHPC, tetra (meso-hydroxy) phenyl chlorin BPD-MA, benzoporphyrin derivative Photofrin is a mixture of several compounds where dimers or trimers of the indicated structure are assumed to be of major importance PpIX, protoporphyrin IX - accumulating upon treatment with 5-aminolevulinic acid or its ester derivatives, NPe6, HPPH, Hexyl pyropheophorbide TPPS2a, disulfonated (adjacent) tetraphenylporphin AlPcS2a, disulfonated (adjacent) aluminum phthalocyanine. Areas with ionic side groups are indicated in shadow... Fig. 2 Examples of photosensitizers presently approved for clinical applications or in clinical studies. mTHPC, tetra (meso-hydroxy) phenyl chlorin BPD-MA, benzoporphyrin derivative Photofrin is a mixture of several compounds where dimers or trimers of the indicated structure are assumed to be of major importance PpIX, protoporphyrin IX - accumulating upon treatment with 5-aminolevulinic acid or its ester derivatives, NPe6, HPPH, Hexyl pyropheophorbide TPPS2a, disulfonated (adjacent) tetraphenylporphin AlPcS2a, disulfonated (adjacent) aluminum phthalocyanine. Areas with ionic side groups are indicated in shadow...
Richter AM, Cerruti-Sola S, Sternberg ED, Dolphin D, Levy JG. Biodistribution of tritiated benzoporphyrin derivative (3H-BPD-MA), a new potent photosensitizer, in normal and tumor-bearing mice. J Photochem Photobiol B 1990 5 231-244. [Pg.139]

Benzoporphyrin derivative monoacid ring A (BPD-MA) Verteporfin Visudyne QLT Inc. Novartis Opthalmic 690... [Pg.10]

H. Lui, L. Hruza, D. McLean, M. Grossman, G. Hruza, K. Gelmon, N. Kollias, J. Wimberly, M. Gagel, R.R. Anderson (1995). Photodynamic therapy of malignant skin tumors with BPD verteporfin (benzoporphyrin derivative). Laser Surg. Med., 7 (Suppl), 44. [Pg.208]

Note Abbreviations are as follows DPPC, diplamitoyl-phosphatidylcholine DMPC, dimiristoyl-phosphatidylcholine POPC, monooleyl-monopalmitoyl-phosphatidylcholine OOPS, dioleyl-phosphatidylserine LDL, low-density lipoproteins Hp, hematoporphyrin ZnPc, Zn(II)-phthaloq anine SnETj, Sn(IV)-etiopurpurin and BPD, benzoporphyrin derivative. [Pg.2838]

Note Photosensitizers are as follows Photofrin , polyhematoporphyrin ethers ALA, aminolevulinic acid mTHPc, meta-tetetrahydroxyphenylchlo-rin SnET2, tin etiopurpurin, Lutetium Texaphyrin, a pendadentate aromatic metalloporphyrin BPD-MA, benzoporphyrin derivative mono acid HPPH, 2-[l-hexyloxyethyl]-devinylpyropheophorbide-a PC4, a silicon phthalocyanine AMD, age-related macular degeneration. [Pg.2846]

Richter, A.M., Waterfield, E., Jain, A.K., Canaan, A.J., Allison, B.A., and Levy, J.G., Liposomal delivery of a photosensitizer, benzoporphyrin derivative monoacid ring A (BPD) to tumor tissue... [Pg.2858]

See other pages where Benzoporphyrin Derivatives BPD is mentioned: [Pg.17]    [Pg.283]    [Pg.255]    [Pg.59]    [Pg.67]    [Pg.157]    [Pg.170]    [Pg.170]    [Pg.245]    [Pg.246]    [Pg.248]    [Pg.139]    [Pg.2826]    [Pg.17]    [Pg.283]    [Pg.255]    [Pg.59]    [Pg.67]    [Pg.157]    [Pg.170]    [Pg.170]    [Pg.245]    [Pg.246]    [Pg.248]    [Pg.139]    [Pg.2826]    [Pg.265]    [Pg.269]    [Pg.221]    [Pg.130]    [Pg.192]    [Pg.199]    [Pg.67]    [Pg.78]    [Pg.85]    [Pg.179]    [Pg.192]    [Pg.582]    [Pg.171]    [Pg.228]    [Pg.2793]    [Pg.2807]   


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