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Submit ReviewLY 233053 is a competitive NMDA receptor antagonist (IC50 = 7 nM) that displays no affinity for AMPA or kainate receptors at a concentration of 10 μM. Inhibits NMDA-induced neuronal degeneration and protects from NMDA-induced convulsions in neonatal rats.
Sold with the permission of Eli Lilly and Company
分子量 | 211.22 |
公式 | C8H13N5O2 |
储存 | Desiccate at RT |
纯度 | ≥99% (HPLC) |
CAS Number | 125546-04-5 |
PubChem ID | 90479799 |
InChI Key | RTVQJOXSBRCZBN-JUKSSJACSA-N |
Smiles | O=[C@@]([C@@H]1C[C@H](CC2=NN=NN2)CCN1)O.O=C([C@H]3C[C@@H](CC4=NN=NN4)CCN3)O |
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Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
Schoepp et al (1990) Pharmacological characterization of LY233053: a structurally novel tetrazole-substituted competitive N-MthD.-aspartic acid antagonist with a short duration of action. J.Pharmacol.Exp.Ther. 255 1301 PMID: 2148188
Madden et al (1992) Efficacy of LY233053, a competitive glutamate antagonist, in experimental central nervous system ischemia. J.Neurosurg. 76 106 PMID: 1727148
Madden et al (1993) Delayed therapy of experimental ischemia with competitive N-MthD.-aspartate antagonists in rabbits. Stroke 24 1068 PMID: 8322381
关键词: LY 233053, LY 233053 supplier, Competitive, NMDA, receptor, antagonists, Glutamate, Receptors, N-Methyl-D-Aspartate, iGlur, Ionotropic, LY233053, 1521, Tocris Bioscience
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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!
*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。
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