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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 | 50 mg |
| Formula Weight | 397.19 |
| Purity | >98% |
| Molecular Weight (g/mol) | 398.195 |
| Chemical Name or Material | Gavestinel |
Safety and Handling
| Recommended Storage | Desiccate at Room Temperature |
Product Title
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