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A novel series of cyclic benzamidines was synthesized and shown to exhibit NR2B-subtype selective NMDA antagonist activity. Compound
29 is orally active in a carrageenan-induced rat hyperalgesia model of pain.
A novel series of cyclic benzamidines was synthesized and shown to exhibit NR2B-subtype selective NMDA antagonist activity. Compound
29 is orally active in a carrageenan-induced rat hyperalgesia model of pain.