O-Acetylgalanthamine
CAS No. 25650-83-3
O-Acetylgalanthamine( —— )
Catalog No. M24153 CAS No. 25650-83-3
The O-Acetylgalanthamine is a natural product that have been found in bulbs of Narcissus pseudonarcissu.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 372 | In Stock |
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| 5MG | 244 | In Stock |
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| 10MG | 361 | In Stock |
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| 25MG | 606 | In Stock |
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| 50MG | 828 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameO-Acetylgalanthamine
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NoteResearch use only, not for human use.
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Brief DescriptionThe O-Acetylgalanthamine is a natural product that have been found in bulbs of Narcissus pseudonarcissu.
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DescriptionThe O-Acetylgalanthamine is a natural product that have been found in bulbs of Narcissus pseudonarcissu.
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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 Number25650-83-3
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Formula Weight329.39
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Molecular FormulaC19H23NO4
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(O[C@H]1C=C[C@@]2(CCN(C)Cc3ccc4OC)c3c4O[C@H]2C1)=O
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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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7,4-Dihydroxyhomoiso...
7,4'-Dihydroxyhomoisoflavane is a natural antioxidant. 7,4'-Dihydroxyhomoisoflavane has ABTS radical-scavenging capacity with an IC50 of 0.22 mg/mL.
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(R)-Omeprazole Sodiu...
(R)-Omeprazole (sodium) (Standard) is the analytical standard of (R)-Omeprazole (sodium). This product is intended for research and analytical applications. (R)-Omeprazole sodium is a gastric acid resistant compound with activity to inhibit gastric acid secretion. (R)-Omeprazole sodium is metabolized in vivo, and its metabolism is primarily affected by cytochrome P450 enzymes. The interaction between (R)-Omeprazole sodium and mannitol may affect its bioavailability in formulations. (R)-Omeprazole sodium exhibits reversible direct and metabolism-dependent inhibition of CYP2C19.
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