D-tetrahydropalmatine
CAS No. 3520-14-7
D-tetrahydropalmatine( —— )
Catalog No. M21452 CAS No. 3520-14-7
D-Tetrahydropalmatine is a organic cation transporter 1 (OCT1) inhibitor it can obviously inhibit the uptake of monocrotaline (MCT) in MDCK-hOCT1 cells and isolate rat primary hepatocytes and attenuate the viability reduction and LDH release of the primary cultured rat hepatocytes caused by MCT.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 86 | Get Quote |
|
| 10MG | 149 | Get Quote |
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| 25MG | 287 | Get Quote |
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| 50MG | 431 | Get Quote |
|
| 100MG | 619 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameD-tetrahydropalmatine
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NoteResearch use only, not for human use.
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Brief DescriptionD-Tetrahydropalmatine is a organic cation transporter 1 (OCT1) inhibitor it can obviously inhibit the uptake of monocrotaline (MCT) in MDCK-hOCT1 cells and isolate rat primary hepatocytes and attenuate the viability reduction and LDH release of the primary cultured rat hepatocytes caused by MCT.
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DescriptionD-Tetrahydropalmatine is a organic cation transporter 1 (OCT1) inhibitor it can obviously inhibit the uptake of monocrotaline (MCT) in MDCK-hOCT1 cells and isolate rat primary hepatocytes and attenuate the viability reduction and LDH release of the primary cultured rat hepatocytes caused by MCT.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number3520-14-7
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Formula Weight355.4
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Molecular FormulaC21H25NO4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (140.67 mM)
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SMILESCOc(ccc(C1)c2CN(CC3)[C@H]1c(cc1OC)c3cc1OC)c2OC
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Tu M Sun S Wang K et al. Organic cation transporter 1 mediates the uptake of monocrotaline and plays an important role in its hepatotoxicity[J]. Toxicology 2013 311(3):225-230.
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