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Dihydropalmatine
CAS No. 26067-60-7
Dihydropalmatine( ZINC689644 | 2,3,9,10-tetramethoxy-6,8-dihydro-5H-isoquinolino[2,1-b]isoquinoline )
Catalog No. M29130 CAS No. 26067-60-7
Dihydropalmatine is a natural product derived from the roots and stem barks of Berberis aristata.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 109 | Get Quote |
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| 10MG | 186 | Get Quote |
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| 25MG | 314 | Get Quote |
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| 50MG | 440 | Get Quote |
|
| 100MG | 597 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameDihydropalmatine
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NoteResearch use only, not for human use.
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Brief DescriptionDihydropalmatine is a natural product derived from the roots and stem barks of Berberis aristata.
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DescriptionDihydropalmatine is a natural product derived from the roots and stem barks of Berberis aristata.(In Vitro):Dihydropalmatine is a metabolic alkaloid of B. aristata and can be identified quickly by the technique of DART MS followed by PCA.
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In Vitro——
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In Vivo——
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SynonymsZINC689644 | 2,3,9,10-tetramethoxy-6,8-dihydro-5H-isoquinolino[2,1-b]isoquinoline
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number26067-60-7
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Formula Weight353.418
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Molecular FormulaC21H23NO4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 25 mg/mL (70.74 mM)
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SMILESCOc1cc2CCN3Cc4c(OC)c(OC)ccc4C=C3c2cc1OC
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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
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Gap19 TFA (1507930-5...
Gap19 TFA is a peptide derived from nine amino acids of Cx43 cytoplasmic ring (CL), an effective, selective connexin 43 (Cx43) half-channel blocker.
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Catalposide
Catalposide is a potent inducer of (HO)-1 isolated from Catalpa ovate G. Don (Bignoniaceae). Catalposide possesses antioxidant, anti-apoptotic, anti-microbial, anti-tumoral, and anti-inflammatory properties.
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ShK-Dap22
Extremely potent KV1.3 channel blocker (Kd = 23 pM for mKV1.3 currents). Selective for KV1.3 over other mammalian potassium channels (IC50 values are 23, 1800, 10500, 37000 and 39000 pM for mKV1.3, mKV1.1, hKV1.6, mKV1.4 and rKV1.2 respectively, and >100000 pM for hKV1.5, mKV1.7, hKV3.1, rKV3.4 and hKCa4). Suppresses T cell activation in vitro (IC50 < 500 pM).
