| 产品详情 |
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| Product Name | CPCCOEt |
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| Description | Purity ~98% (HPLC). A potent, negative allosteric modulator selective for mGlu1 receptors (IC50 = 6.5uM). No effect on other mGlu subtype receptors and ionotropic glutamate receptors at concentrations less than 100uM. Acts by inhibiting an intramolecular interaction between the agonist-bound extracellular domain and the transmembrane domain. Widely used for studies related to peripheral pain and central pain pathways. Formula: C13H13NO4 Solubility: DMSO Primary Target: mGlu1 receptors Molar Mass: 247.25 |
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| Size | 5mg |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | CPCCOEt ((E)-Ethyl 1,1a,7,7a-tetrahydro-7-(hydroxyimino)cyclopropa[b]chromene-1a-carboxylate, mGlu1 Antagonist, CPCCOEt) |
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| Gene, Accession, CAS # | n/a |
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| Catalog # | 217283 |
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| Price | |
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| Order / More Info | CPCCOEt from UNITED STATES BIOLOGICAL |
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| Product Specific References | n/a |
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