Jatrorrhizine chloride

CAS No. 6681-15-8

Jatrorrhizine chloride( Neprotine chloride | Yatrorhizine chloride )

Catalog No. M21537 CAS No. 6681-15-8

Jatrorrhizine chloride is a potent and orally active uptake-2 transporter inhibitor. It exhibits a critical neuroprotective role in H2O2-induced apoptosis via inhibition of the MAPK pathway in HT22 hippocampal neurons.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 35 In Stock
10MG 58 In Stock
25MG 104 In Stock
50MG 160 In Stock
100MG 241 In Stock
500MG 498 In Stock
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Biological Information

  • Product Name
    Jatrorrhizine chloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Jatrorrhizine chloride is a potent and orally active uptake-2 transporter inhibitor. It exhibits a critical neuroprotective role in H2O2-induced apoptosis via inhibition of the MAPK pathway in HT22 hippocampal neurons.
  • Description
    Jatrorrhizine chloride is a potent and orally active uptake-2 transporter inhibitor. It exhibits a critical neuroprotective role in H2O2-induced apoptosis via inhibition of the MAPK pathway in HT22 hippocampal neurons.
  • In Vitro
    Jatrorrhizine has antiplasmodial and antiamoebic activity, it against Plasmodium falciparum and E. histolytica with IC50 values of 3.15 and 82.7 μM, respectively.The hOCT2 (organic cation transporter 2), hOCT3, and PMAT (plasma membrane monoamine transporter) are capable of transporting monoamine neurotransmitters in the brain.Jatrorrhizine has the inhibitory potency of jatrorrhizine on 5-HT and NE uptake in hOCT2-, hOCT3-, and PMAT-transfected cells. Jatrorrhizine strongly inhibits PMAT-mediated MPP+ uptake with an IC50 value of 1.05 μM and reduces 5-HT and NE uptake mediated by hOCT2, hOCT3, and hPMAT with IC50 values of 0.1-1 μM (for OCT2 and OCT3) and 1-10 μM (for PMAT).Clearance of neurotransmitters released into the synaptic cleft is defined by two distinct processes. Uptake-1, the common target of current applied antidepressants, is comprised of the serotonin transporter (SERT),the “SERT”, had a high affinity but low capacity to take up [3H]5-HT. Uptake-2 transporters are an important supplementary regulation system in monoamine clearancethought to be the “NET”, has low affinity but high capacity to take up [3H]5-HT into brain slices.Jatrorrhizine significantly inhibited 5-HT and NE uptake in synaptosomes at 25 μM and 50 μM.
  • In Vivo
    Jatrorrhizine chloride (intraperitoneal?injection; 5, 10, 20 mg/kg) can significantly reduce the duration of immobility when compared with vehicle control group in tail suspension test (TST). Animal Model:Male ICR albino mice Dosage:5, 10, 20 mg/kg Administration:Intraperitoneal?injection; 5, 10, 20 mg/kg Result:Reduced immobility period in tail suspension test.
  • Synonyms
    Neprotine chloride | Yatrorhizine chloride
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    OCT| PMAT
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    6681-15-8
  • Formula Weight
    373.8
  • Molecular Formula
    C20H20ClNO4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:5 mg/mL (13.38 mM)
  • SMILES
    COc(ccc1cc(-c(cc2OC)c(CC3)cc2O)[n+]3cc11)c1OC.[Cl-]
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Sun S et al. Jatrorrhizine reduces 5-HT and NE uptake via inhibition of uptake-2 transporters and produces antidepressant-like action in mice. Xenobiotica. 2019 Oct;49(10):1237-1243.
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