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Bacopaside I
CAS No. 382148-47-2
Bacopaside I( —— )
Catalog No. M24340 CAS No. 382148-47-2
Bacopaside I is a saponin isolated from Bacopa monniera.?Bacopaside I is a modulator of Aquaporin-1 channel, has neuroprotective functions, it has anti-Alzheimer's disease.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 249 | In Stock |
|
| 10MG | 426 | In Stock |
|
| 25MG | 683 | In Stock |
|
| 50MG | 888 | In Stock |
|
| 100MG | 1242 | In Stock |
|
| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameBacopaside I
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NoteResearch use only, not for human use.
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Brief DescriptionBacopaside I is a saponin isolated from Bacopa monniera.?Bacopaside I is a modulator of Aquaporin-1 channel, has neuroprotective functions, it has anti-Alzheimer's disease.
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DescriptionBacopaside I is a saponin isolated from Bacopa monniera.?Bacopaside I is a modulator of Aquaporin-1 channel, has neuroprotective functions, it has anti-Alzheimer's disease, it ameliorates cognitive impairment in APP/PS1 mice via immune-mediated clearance of α2-amyloid,exbibits antioxidant properties and free radical scavenging capacity and exerts antidepressant-like effect.
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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 Number382148-47-2
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Formula Weight979.13
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Molecular FormulaC46H74O20S
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESC[C@]12[C@@]34[C@@](CC[C@]1([H])[C@@]5([C@@](C(C)([C@@H](O[C@@]6([H])[C@@H]([C@H]([C@@H](O)CO6)O[C@]7([H])O[C@@H]([C@@H](O)[C@H](O)[C@H]7O)COS(=O)(O)=O)O[C@]8([H])O[C@@H](CO)[C@H](O)[C@H]8O)CC5)C)([H])CC2)C)([H])[C@]9([H])[C@@](OC4)(OC[C@@H](C=C(C)C)[C@@]9(O)C)C3
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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.Vini C Sekhar, Gayathri Viswanathan, Sabulal Baby 1.Insights Into the Molecular Aspects of Neuroprotective Bacoside A and Bacopaside I.Curr Neuropharmacol. 2019;17(5):438-446.
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