Purinyl tetrahydrofurans

Organic compounds -- part of the class 532-570 series – Organic compounds – Chalcogen bonded directly to ring carbon of the purine ring...

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Other Related Categories

544244, 544265, 544277, 544313, 544314, 544317, 544243, 549476, A61K 3152, C07D47318, C07D47330, C07D47334

Type

Patent

Status

active

Patent number

050596900

Description

ABSTRACT:
Antiviral activity is exhibited by compounds having the formula ##STR1## and pharmaceutically acceptable salts thereof wherein R.sub.1 is a purine or pyrimidine base or an analog thereof and R.sub.2 and R.sub.3 are independently hydrogen, --PO.sub.3 H.sub.2 or ##STR2## wherein X.sub.7 is hydrogen, alkyl, substituted alkyl or aryl.

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patent: 4918075 (1990-04-01), Zahler et al.
Ueda et al., "Chemical Conversion of Nucleosides . . . ", Nucleic Acids Research, Symposium #9, 1981, pp. 91-94.
Shuto et al., "Chemical Conversion of Uridine to . . . ", Nucleosides & Nucleotides, 1(3), 263-273 (1982).
Rosenthal et al., "Branched-Chain Sugar Nucleosides . . . ", Canadian Jour. of Chem., vol. 47, pp. 4477-4481 (1969).
Acton et al., "Improved Antitumor Effects . . . ", Jour. Med. Chem., vol. 22, pp. 518-525 (1979).
Bamford et al., "Synthesis and Antiviral Activity . . . ", Jour. Med. Chem., vol. 33, pp. 2494-2501 (1990).
Pudlo et al., "A New Novel Approach Towards . . . ", Tetrahedron Letters, vol. 31, pp. 3101-3104 (1990).
Slusarchyk et al., U.S. Serial No. 322,375 filed 3/13/89.
DeClercq et al., "Targets for the Design of Antiviral Agents", 1983, pp. 203-230.
Herdewijn et al., "Synthesis and Antiviral Activity . . . ", J. Med. Chem., 1985, vol. 28, pp. 550-555.
Takano et al., "Enantio-Controlled Route . . . ", J. Chem. Soc. Chem. Commun., 1988, pp. 189-191.

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