Adenylate analogs as potent anti-herpes virus agents

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

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514 68, 514 70, 514 81, 536 256, 536 265, 536 274, 544264, A61K 3170, C07H 1919, C07H 1920

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active

057338906

ABSTRACT:
Novel adenylate analogs having the following formula are synthesized in the present invention, which are found active against herpes simplex viruses: ##STR1## wherein R.sup.1 is hydroxyl, C.sub.1 -C.sub.4 alkoxy, an amino ester radical of --NHR.sup.3 COOR.sup.4, wherein R.sup.3 is a bivalent C.sub.1 -C.sub.4 saturated hydrocarbon and R.sup.4 is C.sub.1 -C.sub.4 alkyl; and R.sup.2 is hydroxyl, --O.sup.+ NH.sub.4 or ##STR2##

REFERENCES:
Hakimelahi et al., "Design Synthesis, and Structure-Activity Relationship of Novel Dinucleotide Analogues as Agents Against Herpes and Human Immunodeficiency Viruses," J. Medicinal Chem., 38(23), 4648-4659 (Nov. 10, 1995).
Rosenberg et al., "Phosphonylmethoxyalkyl and Phosphonylalkyl Derivatives of Adenine," Coll. Czech. Chem. Comm., 53(11B), 2753-2777 (Nov. 1988).

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