Results 171 to 180 of about 3,607 (204)
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Synthesis and Properties of Pheophorbide-Quinone Compounds
Bulletin of the Chemical Society of Japan, 1992Abstract New pheophorbide-quinone derivatives with a different kind of quinone moieties were synthesized by mixed anhydride method. The structures of these compounds were confirmed by UV, IR, 1H NMR, fluorescence, and mass spectra. Effective fluorescence quenching of the pheophorbide chromophores in the synthesized molecules was observed
Victor V Borovkov +5 more
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Synthesis of the conjugate of ortho-isobornylphenol with pheophorbide (a)
Mendeleev Communications, 2006The introduction of a terpenophenolic fragment to the periphery of a chlorin cycle has been carried out.
Evgeny V. Buravlev +3 more
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Light-Harvesting Nanorods Based on Pheophorbide-Appending Cellulose
Biomacromolecules, 2013In contrast to the success in artificial DNA- and peptide-based nanostructures, the ability of polysaccharides to self-assemble into one-, two-, and three-dimensional nanostructures are limited. Here, we describe a strategy for designing and fabricating nanorods using a regioselectively functionalized cellulose derivative at the air-water interface in ...
Keita, Sakakibara +10 more
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Photocytotoxic Pheophorbide-Related Compounds fromAglaonema simplex
Chemistry & Biodiversity, 2005In our screening program for new photosensitizers from the Malaysian biodiversity, we found five pheophorbide-related compounds from the leaves and stems of Aglaonema simplex. Detailed spectroscopic analyses showed that compounds 1-3 and 5 are pheophorbide and hydroxy pheophorbide derivatives of chlorophyll a and b.
Chin-Fei, Chee +3 more
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Purification of chlorophylls, pheophytins and pheophorbides for specific activity determinations
Biochimica et Biophysica Acta, 1962Abstract Methods for the purification of 14 C-labelled chlorophylls a and b and of their respective pheophytins, pheophorbides and pyropheophorbides, to constant specific activity are presented. Data are provided showing the specific activities of these compounds obtained from a variety of plants which had been fed [I- 14 C]acetate, [2- 14 C ...
H J, PERKINS, D W, ROBERTS
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Potent virucidal effect of pheophorbide a and pyropheophorbide a on enveloped viruses
Journal of Natural Medicines, 2010In this study, we evaluated the inhibitory effect of ethanol and aqueous extracts from a stem of Opuntia ficus indica on replication of three kinds of viruses: two enveloped viruses [herpes simplex virus type 2 (HSV-2), influenza A virus (IFV-A)], and one non-enveloped virus [poliovirus type 1 (PV-1)].
Lamjed, Bouslama +4 more
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Effective photocleavage of DNA by pheophorbide a.
Nucleic acids symposium series, 1992Remarkably effective photocleavage of plasmid DNA with pheophorbide a, as a visible light sensitizer, has been found for the first time. DNA is photocleaved even in the absence of oxygen. The novel oxygen-independent scission is ascribed to specific photodynamic function of the ring V in pheophorbide a.
M, Kobayashi, M, Harada, M, Komiyama
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Electrophilic substitution at the δ-methine bridge of pheophorbide and ′
Tetrahedron Letters, 1981Abstract A chloro-substituted derivative was prepared from chlorophyll a ′. The derivative was shown to be δ-chloro-methyl pheophorbide a by UV/VIS, MS and ′H NMR.
Paavo H. Hynninen, Simo Lötjönen
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Pheophorbides as photosensitizers for the photodynamic therapy of tumors
Proceedings of SPIE, 1995Quantum yields for formation of singlet molecular oxygen have been measured for sodium pheophorbides (Na-Phdes) a and b in aqueous and non-aqueous media. Measurements have been made for both steady-state and pulsed laser excitation with the resultant singlet molecular oxygen being detected by photo-oxygenation reactions or time-resolved luminescence ...
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Transesterification of the α-keto ester in methyl pheophorbide-a
Tetrahedron Letters, 1996Abstract Transesterification of the α-keto methyl ester in methyl pheophorbide-a proceeds smoothly under neutral conditions, allowing the preparation of a variety of models such as steroid-pheophorbide, pyromellitimide-pheophorbide, thymidine-pheophorbide, pheophorbide dimer, and porphyrin-pheophorbide.
Satoshi Shinoda, Atsuhiro Osuka
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