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Description
Highly potent and selective non-competitive antagonist acting at the strychnine-insensitive glycine binding site of the NMDA receptor-channel complex (Kd = 0.8 nM). Displays > 1000-fold selectivity over NMDA, AMPA and kainate binding sites. Orally bioavailable and active in vivo.

Specifications
Specifications
Quantity | 10 mg |
Formula Weight | 397.19 |
Percent Purity | >98% |
Chemical Name or Material | Gavestinel |
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Product Title
Gavestinel, Tocris Bioscience™ >
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