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
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 50 In Stock
2MG 29 In Stock
5MG 46 In Stock
10MG 79 In Stock
25MG 170 In Stock
50MG 269 In Stock
100MG 415 In Stock
200MG 600 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

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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