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Submit ReviewNMDA receptor antagonist (IC50 = 0.4 μM) that displays > 100 fold selectivity for GluN2B (formally NR2B) containing receptors over GluN2A (formally NR2A) containing receptors. Exhibits an activity-dependent mechanism of NMDA antagonism and is competitive with respect to spermine (Cat. No. 0958).
Please refer to IUPHAR Guide to Pharmacology for the most recent naming conventions.
M. Wt | 406.88 |
Formula | C21H23FN2O3.HCl |
Storage | Desiccate at RT |
Purity | ≥99% (HPLC) |
CAS Number | 1312991-77-7 |
PubChem ID | 11957680 |
InChI Key | MQOXWHKUQOFFJW-UHFFFAOYSA-N |
Smiles | NC(C1=CC=C(OCC(O)CN2CCC(C3=CC=C(F)C=C3)=CC2)C=C1)=O.Cl |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
References are publications that support the biological activity of the product.
Kew et al (1998) State-dependent NMDA receptor antagonism by Ro 8-4304, a novel NR2B selective, non-competitive, voltage-independent antagonist. Br.J.Pharmacol. 123 463 PMID: 9504387
Kew and Kemp (1998) An allosteric interaction between the NMDA receptor polyamine and ifenprodil sites in rat cultured cortical neurones. J.Physiol. 512 17 PMID: 9729614
Keywords: Ro 8-4304 hydrochloride, Ro 8-4304 hydrochloride supplier, NR2B, selective, antagonists, NMDA, Receptors, Glutamate, Ionotropic, N-Methyl-D-Aspartate, iGluR, Ro8-4304, GluN2B, 3343, Tocris Bioscience
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