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| Product | Description | |
|---|---|---|
| CPCCOEt | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| CPCCOEt | CPCCOEt has been found to be a mGluR-1 antagonist. Synonyms: 7-(Hydroxyimino)cyclopropa[b]chromen-1a-carboxylate ethyl ester. Grades: ≥99% by HPLC. CAS No. 179067-99-3. Molecular formula: C13H13NO4. Mole weight: 247.25. |  |
| CPCCOEt | CPCCOEt is a low affinity, selective, non-competitive and reversible antagonist of metabotropic glutamate receptor 1b (mGluR1b) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 179067-99-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-101356. |  |
| CPCCOEt ((E)-Ethyl 1, 1a, 7, 7a-tetrahydro-7- (hydroxyimino) cyclopropa[b]chromene-1a-carboxylate, mGlu1 Antagonist, CPCCOEt) | 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. Group: Biochemicals. Grades: Highly Purified. CAS No. 179067-99-3. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
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