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CPCCOEt

🥰Excellent
Catalog No. T22692Cas No. 179067-99-3

CPCCOEt is a low-affinity, selective, non-competitive, and reversible antagonist of mGluR1b.

CPCCOEt

CPCCOEt

🥰Excellent
Purity: 99.87%
Catalog No. T22692Cas No. 179067-99-3
CPCCOEt is a low-affinity, selective, non-competitive, and reversible antagonist of mGluR1b.
Pack SizePriceAvailabilityQuantity
5 mg$48In Stock
10 mg$67In Stock
25 mg$136In Stock
50 mg$223In Stock
100 mg$329In Stock
1 mL x 10 mM (in DMSO)$48In Stock
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Purity:99.87%
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Product Introduction

Bioactivity
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].
Chemical Properties
Molecular Weight247.25
FormulaC13H13NO4
Cas No.179067-99-3
SmilesCCOC(=O)C12CC1\C(=N/O)c1ccccc1O2
Relative Density.1.42g/cm3
Storage & Solubility Information
StoragePowder: -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
1mg5mg10mg50mg
1 mM4.0445 mL20.2224 mL40.4449 mL202.2245 mL
5 mM0.8089 mL4.0445 mL8.0890 mL40.4449 mL
10 mM0.4044 mL2.0222 mL4.0445 mL20.2224 mL
20 mM0.2022 mL1.0111 mL2.0222 mL10.1112 mL
50 mM0.0809 mL0.4044 mL0.8089 mL4.0445 mL
100 mM0.0404 mL0.2022 mL0.4044 mL2.0222 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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