CPCCOEt

CAS No. 179067-99-3

CPCCOEt( —— )

Catalog No. M33842 CAS No. 179067-99-3

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

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 46 In Stock
10MG 64 In Stock
25MG 125 In Stock
50MG 205 In Stock
100MG 296 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CPCCOEt
  • Note
    Research use only, not for human use.
  • Brief Description
    CPCCOEt is a low-affinity, selective, non-competitive, and reversible antagonist of mGluR1b.
  • Description
    CPCCOEt is a low affinity, selective, non-competitive and reversible antagonist ofmetabotropic glutamate receptor 1b (mGluR1b).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Neuroscience
  • Target
    GluR
  • Recptor
    GluR
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    179067-99-3
  • Formula Weight
    247.25
  • Molecular Formula
    C13H13NO4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (404.45 mM; Ultrasonic )
  • SMILES
    CCOC(=O)C12CC1\C(=N/O)c1ccccc1O2
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Litschig S, et al. CPCCOEt, a noncompetitive metabotropic glutamate receptor 1 antagonist, inhibits receptor signaling without affecting glutamate binding. Mol Pharmacol. 1999 Mar;55(3):453-61.??
molnova catalog
related products
  • VU6005649

    VU6005649 is an agonist of CNS penetrant mGlu7/8 receptor (EC50s: 0.65 μM and 2.6 μM for mGlu7 receptor and mGlu8 receptor, respectively).

  • lavendustin B

    Lavendustin B is a Tyrosine Kinase Inhibitor and an inhibitor of HIV-1 integrase (IN) interaction with its cognate cellular cofactor, lens epithelium-derived growth factor (LEDGF/p75).

  • JNJ16259685

    JNJ16259685 is a selective mGluR1 antagonist, and inhibits the synaptic activation of mGluR1 in a concentration-dependent manner with IC50 of 19 nM.