Tetraphenylbacteriochlorin derivatives and compositions...

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

Reexamination Certificate

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C536S017100, C536S018500

Reexamination Certificate

active

06958389

ABSTRACT:
Provided is a tetraphenylbacteriochlorin derivative represented by the formula (I):[wherein R1, R2, R3and R4, independently from each other, are a residue of a monosaccharide represented by the formulae:(wherein, R is a hydrogen or a protecting group)], or its salt. The tetraphenylbacteriochlorin derivative or its salt has a large molar extinction coefficient at long wavelengths which are expected to have a high tissue-penetrating property, and exhibits high selectivity to tumor cells and hydrophilicity.

REFERENCES:
patent: 2000-007693 (2000-01-01), None
patent: WO 96/13504 (1996-05-01), None
Bonar-Law, Richard P. et al., “Morphine Recognition by a Porphyrin-Cyclocholate Molecular Bowl”, J. Chem. Soc., Chem. Commun., pp. 456-458, (1993).
Datta-Gupta, Nirmalendu et al., “Oxidation of meso-Tetraphenylchlorins by Dimethyl Sulfoxide to the Corresponding meso-Porphyrins”, J. Org. Chem., vol. 36, No. 14, pp. 2019-2021, (1971).
Gong, Liang-Chu et al., “Nitrooctaethylporphyrins: synthesis, optical and redox properties”, Can. J. Chem., vol. 63, pp. 401-405, (1985).
Zhang, Xiao-Bing et al., “Synthesis of acetylglycosylated metalloporphyrins and their catalysis for cyclohexane oxidation with PhIO under mild conditions”, Journal of Molecular Catalsis A: Chemical, vol. 154, pp. 31-38, (1999).
Y. Mikata et al., Tetrahedron Letters, 39, 1998, pp. 4505-4508.
H.W. Whitlock et al., Journal of the American Chemical Society, vol. 91, No. 26, Dec. 17, 1969, pp. 7485-7489.

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