R-NSAID esters and their use

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C549S317000, C549S292000, C546S238000, C560S051000, C560S056000, C560S100000, C560S102000, C560S112000, C514S532000, C514S545000, C514S544000

Reexamination Certificate

active

07074826

ABSTRACT:
The present invention concerns esters of R-enantiomers of a non-steroidal anti-inflammatory drug, which is substantially free from the S-enantiomer. The compounds of the invention may be used in treating a disease or illness in a mammal. To this end, a composition comprising a compound mentioned above, or a pharmaceutically acceptable salt thereof where salt formation occurs, is administered to the mammal in an amount sufficient to elicit a chemopreventative effect or a chemoprotective effect or a therapeutic effect or a prophylactic effect.

REFERENCES:
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patent: 2003/0027867 (2003-02-01), Zavitz
patent: 0 305 089 (1989-03-01), None
Wechter et al, Cancer Research,vol. 60, p. 2203-2208, Apr. 15, 2001.
Kato, et al., Studies on Scavengers of Active Oxygen Species. 1. Synthesis and Biological Activity of 2-O-Alkylascorbic Acids,J. Med. Chem., 31:793-798 (1988).
Manfredini, et al., Novel Antiosidant Agents Deriving From Molecular Combinations of Vitamins C and E Analogues: 3,4-Dihydroxy-5(R)-[2(R,S)-(6-hydroxy-2,5,7,8-tetramethylchroman-2(R,S)-yl-methyl)-[1,3]dioxolan-4(S)-yl]-5H-furan-2-one and 3-O-Octadecyl Deerivatives,Bioorganic&Medical Chemistry, 8:2791-2801 (2000).
Manfredini, et al., Design, Synthesis and Activity of Ascorbic Acid Prodrugs of Nipecotic, Kinurenic and Diclophenamic Acids, Liable to Increase Neurotropic Activity,Journal of Medicinal Chemistry, (Nov. 2001).

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