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CPCCOEt is a low-affinity, selective, non-competitive, and reversible antagonist of mGluR1b.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
5 mg | $48 | In Stock | |
10 mg | $67 | In Stock | |
25 mg | $136 | In Stock | |
50 mg | $223 | In Stock | |
100 mg | $329 | In Stock | |
1 mL x 10 mM (in DMSO) | $48 | In Stock |
Description | CPCCOEt is a low-affinity, selective, non-competitive, and reversible antagonist of mGluR1b. |
Targets&IC50 | mGluR1b (human):6.5 μM |
In vitro | CPCCOEt selectively inhibited glutamate-induced increases in intracellular calcium at human mGluR1b (hmGluR1b) with an apparent IC50 of 6.5 μM while having no agonist or antagonist activity at hmGluR2, -4a, -5a, -7b, and -8a up to 100 μM. In addition, introduction of Thr815 and Ala818 at the homologous positions of hmGluR5a conferred complete inhibition by CPCCOEt (IC50 = 6.6 μM)[1]. |
In vivo | Whole-cell voltage recording from Purkinje cells in slices of rat cerebellum showed that CPCCOEt enhanced the climbing fiber response at concentrations of blocking the mGlu1 receptor(100 μM)[2]. |
Molecular Weight | 247.25 |
Formula | C13H13NO4 |
Cas No. | 179067-99-3 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
Solubility Information | DMSO: 90.0 mg/mL (364.0 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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