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Submit ReviewHigh affinity antagonist at the ion channel on the NMDA receptor.
M. Wt | 381.47 |
Formula | C19H23N.C4H4O4 |
Storage | Store at RT |
CAS Number | 207461-99-2 |
PubChem ID | 16657069 |
InChI Key | AEHZEDLXDLPQQD-BTJKTKAUSA-N |
Smiles | OC(=O)\C=C/C(O)=O.C(C(N1CCCCC1)C1=CC=CC=C1)C1=CC=CC=C1 |
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.
Ragawski (1993) Therapeutic potential of excitatory amino acid antagonists: channel blockers and 2,3-benzodiazepines. TiPS 14 325 PMID: 7504360
Keywords: (±)-1-(1,2-Diphenylethyl)piperidine maleate, (±)-1-(1,2-Diphenylethyl)piperidine maleate supplier, NMDA, antagonists, ion, channel, site, Glutamate, Receptors, N-Methyl-D-Aspartate, iGluR, Ionotropic, 0360, Tocris Bioscience
Citations are publications that use Tocris products. Selected citations for (±)-1-(1,2-Diphenylethyl)piperidine maleate include:
Ataka et al (2012) Alteration of antral and proximal colonic motility induced by chronic psychological stress involves central urocortin 3 and vasopressin in rats. Am J Physiol Gastrointest Liver Physiol 303 G519 PMID: 22651925
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
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This product guide provides a background to Huntington's disease research and lists around 100 products for the study of:
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