Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.
Visit our FAQ
Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888
Product Categories
Research Area
Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.
Bitopertin is an inhibitor of glycine transporter 1 (GlyT1; IC50 = 0.03 µM).1 It is selective for GlyT1 over GlyT2 (IC50 = >30 µM) as well as a panel of 107 receptors, transporters, and enzymes at 10 µM.1,2 Bitopertin (0.1 µM) increases long-term potentiation in rat hippocampal CA1 slices.2 It reverses hyperlocomotion induced by the NMDA receptor partial agonist L-687,414 in mice (ID50 = 0.5 mg/kg).1
WARNING This product is not for human or veterinary use.
1. Selective GlyT1 inhibitors: Discovery of [4-
2. Glycine reuptake inhibitor RG1678: A pharmacologic characterization of an investigational agent for the treatment of schizophrenia. Neuropharmacology 62(2), 1152-1161 (2012).