Substituted γ-lactone compounds as NMDA-antagonists

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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C514S255050, C514S275000, C514S313000, C514S336000, C514S407000, C544S332000, C544S336000, C546S159000, C546S284400, C548S371400, C549S303000, C549S321000

Reexamination Certificate

active

06956055

ABSTRACT:
The invention relates to substituted γ-lactone compounds, to methods for the production thereof, to medicaments containing these compounds and to the use of these compounds for producing medicaments.

REFERENCES:
patent: 0386839 (1997-01-01), None
patent: WO 97/12879 (1997-04-01), None
patent: WO 98/07704 (1998-02-01), None
patent: WO 98/42673 (1998-10-01), None
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“A New Synthesis Of Amino Acids. II. Amidoalkylation of Olefins With Glyoxylic Acid Derivatives”, Ben-Ishai et al., Tetrahedron Lett. 1975, vol. 33, pp. 1533-1442.
“Amino Acid Synthesis II. Amidoalkylation Of Olefins With Glyoxylic Acid Derivatives”, Altman et al., Tetrahedron Lett. 1975, No. 43, PP. 3737-3740.
“Relationship Between the Inhibition Constant (K1) and the Concentration of Inhibitor Which Causes 50 per cent Inhibition (I50) of an Enzymatic Reaction”, Cheng et al., Biochemical Pharmacology, vol. 22, pp. 3099-3108, 1973.
2-Carboxytetrahydroquinolines. Conformational and Stereochemical Requirements for Antagonism of the Glycine Site on the NMDA Receptor, Carling et al., J. Med. Chem. 1992, 35, pp. 1942-1953.
“[3H]MDL 105,519, a High-Affinity Radioligand for the N-Methyl-D-aspartate Receptor-Associated Glycine Recognition Site”, Baron et al., Jnl of Pharm. And Experimental Therapeutics, 1996, pp. 62-68.

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