Uridine derivatives as antibiotics

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

Reexamination Certificate

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Details

C514S049000, C536S028400, C536S028530

Reexamination Certificate

active

06875752

ABSTRACT:
All possible isomeric forms of a compound of the formulawhere the substituents are defined as in the specification and its non-toxic, pharmaceutically acceptable salts useful as antibiotics.

REFERENCES:
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patent: 02 306992 (1990-12-01), None
patent: 05078385 (1993-03-01), None
patent: 05 078385 (1993-03-01), None
patent: 9741248 (1997-11-01), None
Hampton et al., “Design of Species- or Isozyme-Specific Enzyme Inhibitors, Part 1 . . . ”, Journal of Medicinal Chemistry, 1979, vo 22, No. 6, pp. 621-631.*
Hampton et al., “Design of Species- or Isozyme-Specific Enzyme Inhibitors, Part 2 . . . ”, Journal of Medicinal Chemistry, 1979, v 22, No. 12, pp. 1524-1528.*
M. Ubukata et al, “The . . . Synthesis”, J. Am. Chem. Soc. vol. 110, No. 13, 1988, pp. 4416-4417.
Imura et al, “Liposidomycin . . .coliY-10”, Agric. Biol. Chem., vol. 53, No. 7, 1989, pp. 1811-1815.
Knapp et al, “Synthesis . . . Diazepanone”, Tetrahedron Letters, vol. 33, No. 35, 1999, pp. 5435-5486.
M. Ubukata, “Chemical . . . Antibiotics”, Journal of Japan Society for Bioscience, Biotechnology and Agrochemistry, vol. 62, No. 11, 1988, pp. 1629-1636, no translation provided.
M. Ubukata et al, “structure . . . Antibiotics”, J. Org. Chem., vol. 57 No. 24, 1992 pp. 6392-6403.

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