Dihydrophthalazine antagonists of excitatory amino acid...

C - Chemistry – Metallurgy – 07 – D

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C07D 237/30 (2006.01) A61K 31/50 (2006.01) C07D 471/04 (2006.01) C07D 487/04 (2006.01) C07D 491/04 (2006.01) C07D 491/056 (2006.01) C07D 498/04 (2006.01)

Patent

CA 2222316

Substituted dihydrophthalazine compositions are provided which are active as non-NMDA ionotropic excitatory amino acid (EAA) receptor antagonists. The compositions are useful for treating disorders associated with excessive activation of the non-NMDA subtype of the ionotropic EAA receptor. The compounds further are useful as testing agents to identify and characterize other compounds for the treatment of these disorders. The compounds are useful therapeutically as sedatives or for the treatment of neuropsychopharmacological disorders such as stroke, ischemia and epilepsy. The compositions may be provided in combination with a suitable carrier for oral or parental administration. The compounds may be administered orally or parenterally for the treatment of a variety of disorders associated with non- NMDA EAA receptor function.

On décrit des compositions de dihydrophatalazine substituée, lesquelles sont actives en tant qu'antagonistes des récepteurs d'acides aminés (EAA) excitateurs ionotropes non sensibles au N-méthyl-D-aspartate (NMDA). Ces compositions sont utiles pour traiter des troubles associés à une activation excessive du sous-type non sensible au NMDA du récepteur d'acide aminé excitateur ionotrope. Ces composés sont en outre utiles en tant qu'agents d'essai pour identifier et caractériser d'autres composés destinés au traitement de ces troubles. Ces composés sont utiles en thérapeutique en tant que sédatifs ou pour le traitement de troubles d'ordre neuropsychologique, tels que l'ictus, l'ischémie et l'épilepsie. On peut ajouter à ces compositions un excipient approprié, aux fins d'administration par voie orale ou parentérale. On peut administrer ces composés, par voie orale ou parentérale, afin de traiter différents troubles associés à la fonction du récepteur d'acide aminé excitateur, non sensible au NMDA.

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