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SCH 50911 is a **selective, competitive, orally-active γ-aminobutyric acid type B (GABA-B) receptor antagonist**. Structurally, it is a novel morpholino-acetic acid derivative developed for research use. SCH 50911 exhibits potent inhibition of GABA binding at the GABA-B receptor, with low micromolar affinity, and shows high selectivity over GABA-A and other central neurotransmitter receptors. In animal studies, it has been used to study GABAergic transmission, absence seizures, and withdrawal syndromes, including for γ-hydroxybutyrate (GHB). Its main application is in pharmacological research, especially neuroscience, epilepsy, and addiction[1][6][7][8][4].
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