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Cyclohexylamine derivatives as antagonists of selective n-methyl-d-aspartate subtypes
Cyclohexylamine derivatives as antagonists of selective n-methyl-d-aspartate subtypes
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机译:环己胺衍生物作为选择性n-甲基-d-天冬氨酸亚型的拮抗剂
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摘要
"CYCLHEXYLAMINE DERIVATIVES AS ANTAGONISTS OF SELECTIVE N-METHYL-D-ASPARTATE SUBTIPOSES". Derivatives of Formula 1 and pharmaceutically acceptable salts thereof are described, wherein R 1, g, R, V, B, E, Y, G, H, X 1, and d are as defined above in the description. . The compounds of Formulas I and VI are NMDA receptor channel complex antagonists useful for the treatment of cerebral vascular disorders such as, for example, stroke, cerebral ischemia, trauma, hypoglycemia, anxiety, migraine, seizures, Parkinson's disease, hearing loss induced by aminoglycoside antibiotics, psychosis, glaucoma, CMV retinitis, opioid tolerance or withdrawal, chronic pain, or urinary incontinence.
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