Lyxofuranosyl analogues of adenosine

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

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536 272, 536 274, 536 2762, 536 2713, 544264, 544254, 544262, 544280, 544265, 544266, 544267, 544271, 544272, 544273, 544277, C07G 300, C07H 1916

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055063470

ABSTRACT:
Novel lyxose derivatives which selectively inhibit adenosine kinase and methods of preparing these compounds are provided. These compounds are useful in treating certain conditions in vivo which may be ameliorated by increased local concentrations of adenosine.

REFERENCES:
Gupta et al., "Relationship Between Structure and Antiviral Activity of 5-Methoxymethyl-2'-Deoxyuridine and 5-Methoxymethyl-1-(2'deoxy-.alpha.-D-lyxofuranosyl)uracil," Antiviral Research, 7, 69-77 (1987).
Ealick et al., "Application of Crystallographic and Modeling Methods in the Design of Purine Nucleoside Phosphorylase Inhibitors," Proc. Nat. Acad. Sci. USA, 88, 11540-11544 (1991).
Bennett et al., "Structural Requirments for Activity of Nucleosides as Substrates for Adenosine Kinase. Orientation of Substituents on the Pentofuranosyl Ring," Mol. Pharmacol., 11(6), 803-808 (1975); Chem. Abstr., 84, p. 173, Abstract No. 40185e (1976); only Abstract supplied.
K. H. Scheit, "Nucletides with Altered Sugar Parts. Arabino, Xylo and Lyxo Nucleotide Analogs," Ch. 5.1 in Nucleotide Analogs, Synthesis and Biological Function, Wiley-Interscience, New York, 1980, pp. 151-153 and 190-191.

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