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Product Name | Jatrorrhizine |
Price: | $37 / 20mg |
Catalog No.: | CN02047 |
CAS No.: | 3621-38-3 |
Molecular Formula: | C20H20NO4 |
Molecular Weight: | 338.4 g/mol |
Purity: | >=98% |
Type of Compound: | Alkaloids |
Physical Desc.: | Yellow powder |
Source: | The barks of Phellodendron chinense Schneid. |
Solvent: | Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc. |
SMILES: | COc1cc2c(cc1O)CC[n+]1c2cc2ccc(c(c2c1)OC)OC |
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Description | Jatrorrhizine is a potent and orally active uptake-2 transporter inhibitor, it can be isolated from various Chinese medicinal plants[1]. Jatrorrhizine exhibits a critical neuroprotective role in H2O2-induced apoptosis via inhibition of MAPK pathway in HT22 hippocampal neurons[2]. |
Target | Uptake-2 transporter[1] |
In Vitro | Organic cation transporters (OCTs) and the plasma membrane monoamine transporter (PMAT) are major uptake-2 transporters[1]. Jatrorrhizine significantly inhibits the plasma membrane monoamine transporter (PMAT) -mediated MPP+ uptake in a concentration-dependent manner with an IC50 value of 1.05 μM[1]. Jatrorrhizine demonstrates a more powerful inhibition on serotonin (5-HT) and norepinephrine (NE) uptake mediated by hOCT2 and hOCT3 than that mediated by PMAT[1]. Jatrorrhizine attenuates the H2O2-induced Bcl-2/Bax ratio reduction and caspase-3 activation in these neurons[2]. |
Exact Mass | 338.138672 |
PSA | 51.80000 |
LogP | -1.89 |
Storage condition | 2-8°C |