Madecassoside
CAS No. 34540-22-2
Madecassoside( Asiaticoside A )
Catalog No. M18455 CAS No. 34540-22-2
Madecassoside is a pentacyclic triterpene extracted from Centella asitica (L.) with anti-inflammatory, anti-oxidative and anti-aging activities.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 29 | In Stock |
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| 10MG | 47 | In Stock |
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| 25MG | 85 | In Stock |
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| 50MG | 146 | In Stock |
|
| 100MG | 233 | In Stock |
|
| 200MG | 357 | In Stock |
|
| 500MG | 597 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameMadecassoside
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NoteResearch use only, not for human use.
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Brief DescriptionMadecassoside is a pentacyclic triterpene extracted from Centella asitica (L.) with anti-inflammatory, anti-oxidative and anti-aging activities.
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DescriptionMadecassoside is a pentacyclic triterpene extracted from Centella asitica (L.) with anti-inflammatory, anti-oxidative and anti-aging activities.
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In VitroCell Viability Assay Cell Line:HUVECs Concentration:10, 30, 100 μmol/L Incubation Time:12 h Result:Increased cell viability to 68.9% and 78.3%, with concentration of 30 and 100 μmol/L, respectively.Western Blot Analysis Cell Line:HUVECs Concentration:10, 30, 100 μmol/L Incubation Time:12 h Result:Inhibited phosphorylation in p38 MAPK.
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In VivoAnimal Model:Focal cerebral ischemia reperfusion injury in Sprague Dawley rats Dosage:6, 12, 24 mg/kg Administration:Intravenous injection Result:Reduced neurological deficit, infarct area, brain damage and neuronal apoptosis.Animal Model:Lipopolysaccharide-induced neurotoxicity in Sprague-Dawley rats Dosage:30-120 mg/kg for 14 days Administration:Intraperitoneal injection Result:Reduced LPS-induced cognitive impairment and imflammatory cytokine, promoted Nrf2 pathway at concentration of 120 mg/kg.
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SynonymsAsiaticoside A
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research AreaOthers-Field
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Indication——
Chemical Information
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CAS Number34540-22-2
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Formula Weight975.12
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Molecular FormulaC48H78O20
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Purity>98% (HPLC)
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SolubilityDMSO : ≥ 9.8 mg/mL; 10.05 mM
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SMILES[C@@H]1([C@@H](CC[C@@]2(CC[C@@]3([C@@]4(C[C@H]([C@H]5[C@]([C@H]([C@@H](C[C@@]5([C@H]4CC=C3[C@H]12)C)O)O)(C)CO)O)C)C)C(=O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O[C@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)C)O)O)O)O)O)O)O)O)C)C
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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. Lin X, et al. Pharmacol Biochem Behav. 2014 Sep;124:434-42.
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