Kaempferol 3-glucorhamnoside
CAS No. 40437-72-7
Kaempferol 3-glucorhamnoside( —— )
Catalog No. M21455 CAS No. 40437-72-7
Kaempferol-3-O-glucorhamnoside a flavonoid derived from plant Thesium chinense Turcz inhibits inflammatory responses via MAPK and NF-κB pathways in vitro and in vivo[1]. Kaempferol-3-O-glucorhamnoside exhibits significant antioxidant activity by scavenging stable DPPH free radicals..
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 149 | In Stock |
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| 10MG | 219 | In Stock |
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| 25MG | 357 | In Stock |
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| 50MG | 537 | In Stock |
|
| 100MG | 781 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameKaempferol 3-glucorhamnoside
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NoteResearch use only, not for human use.
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Brief DescriptionKaempferol-3-O-glucorhamnoside a flavonoid derived from plant Thesium chinense Turcz inhibits inflammatory responses via MAPK and NF-κB pathways in vitro and in vivo[1]. Kaempferol-3-O-glucorhamnoside exhibits significant antioxidant activity by scavenging stable DPPH free radicals..
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DescriptionKaempferol-3-O-glucorhamnoside a flavonoid derived from plant Thesium chinense Turcz inhibits inflammatory responses via MAPK and NF-κB pathways in vitro and in vivo[1]. Kaempferol-3-O-glucorhamnoside exhibits significant antioxidant activity by scavenging stable DPPH free radicals..
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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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TargetAntioxidant
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RecptorAntioxidant
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Research Area——
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Indication——
Chemical Information
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CAS Number40437-72-7
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Formula Weight594.5
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Molecular FormulaC27H30O15
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Purity>98% (HPLC)
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SolubilityH2O:1 mg/mL (168.2 mM);DMSO:2 mg/mL (3.36 mM);Ethanol:1 mg/mL (1.68 mM)
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SMILESC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O[C@@H]2[C@@H]([C@H]([C@@H](O[C@H]2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)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
1.Sun Z et al. Kaempferol-3-O-glucorhamnoside inhibits inflammatory responses via MAPK and NF-κB pathways in vitro and in vivo. Toxicol Appl Pharmacol. 2019 Feb 1;364:22-28.
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