Cutamesine dihydrochloride

CAS No. 165377-44-6

Cutamesine dihydrochloride( SA4503 (dihydrochloride) | AGY94806 dihydrochloride )

Catalog No. M17359 CAS No. 165377-44-6

Cutamesine dihydrochloride is a selective σ1 receptor agonist (IC50: 17.4 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Cutamesine dihydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Cutamesine dihydrochloride is a selective σ1 receptor agonist (IC50: 17.4 nM).
  • Description
    Cutamesine dihydrochloride is a selective σ1 receptor agonist (IC50: 17.4 nM). It shows selectivity for σ1 over σ2 receptors, and inhibits angiotensin II-induced cardiomyocyte hypertrophy in vitro and attenuates myocardial hypertrophy in vivo. In a rat model of experimental stroke, it enhances brain plasticity and sensorimotor function.(In Vitro):The sigma receptor might be involved in several diseases in the central nervous system. Cutamesine, a potent σ1receptor agonist, has 103-fold higher affinity for σ1 (IC50=17.4 nM) than σ2 (IC50=1,784 nM) sites in guinea pig brain membranes. Cutamesine is 14-fold selective for σ1 (Ki=4.6 nM) over σ2 (Ki=63.1 nM) sites in guinea pig brain homogenates. Cutamesine protects motor neuron NSC34 cells against superoxide dismutase 1 and serum free neurotoxicity. It upregulates the phosphorylation levels of Akt and extracellular signal-regulated kinase (ERK) 1/2. Cutamesine reduces the activation of the MAPK/ERK pathway and down-regulated the ionotropic glutamate receptor, GluR1.(In Vivo):Cutamesine extends the survival time in the SOD1G93A mice.
  • In Vitro
    The sigma receptor might be involved in several diseases in the central nervous system. Cutamesine, a potent σ1receptor agonist, has 103-fold higher affinity for σ1 (IC50=17.4 nM) than σ2 (IC50=1,784 nM) sites in guinea pig brain membranes. Cutamesine is 14-fold selective for σ1 (Ki=4.6 nM) over σ2 (Ki=63.1 nM) sites in guinea pig brain homogenates. Cutamesine protects motor neuron NSC34 cells against superoxide dismutase 1 and serum free neurotoxicity. It upregulates the phosphorylation levels of Akt and extracellular signal-regulated kinase (ERK) 1/2. Cutamesine reduces the activation of the MAPK/ERK pathway and down-regulated the ionotropic glutamate receptor, GluR1.
  • In Vivo
    Cutamesine extends the survival time in the SOD1G93A mice.
  • Synonyms
    SA4503 (dihydrochloride) | AGY94806 dihydrochloride
  • Pathway
    Neuroscience
  • Target
    GluR
  • Recptor
    σ1
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    165377-44-6
  • Formula Weight
    441.43
  • Molecular Formula
    C23H32N2O2·2HCl
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 30 mg/mL 67.96 mM;
  • SMILES
    COc1c(cc(cc1)CCN1CCN(CC1)CCCc1ccccc1)OC.Cl.Cl
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Tagashira H, et al. Biochim Biophys Acta. 2013, 1830(4):3082-94.
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