Kaempferol 3-O-β-D-glucuronide
CAS No. 22688-78-4
Kaempferol 3-O-β-D-glucuronide( Kaempferol-3-beta-O-glucuronide | Kaempferol-3-glucuronide | Kaempferol-3-O-glucuronide )
Catalog No. M29175 CAS No. 22688-78-4
Kaempferol 3-O-β-D-glucuronidee has antioxidant activity. Flavonoid glucuronides can be deconjugated by microsomal α2-glucuronidase from various human cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 271 | In Stock |
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| 5MG | 264 | In Stock |
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| 10MG | 391 | In Stock |
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| 25MG | 652 | In Stock |
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| 50MG | 909 | In Stock |
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| 100MG | 1228 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameKaempferol 3-O-β-D-glucuronide
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NoteResearch use only, not for human use.
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Brief DescriptionKaempferol 3-O-β-D-glucuronidee has antioxidant activity. Flavonoid glucuronides can be deconjugated by microsomal α2-glucuronidase from various human cells.
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DescriptionKaempferol 3-O-β-D-glucuronidee has antioxidant activity. Flavonoid glucuronides can be deconjugated by microsomal α2-glucuronidase from various human cells.(In Vitro):Kaempferol-3-o-β-d-glucuronate exhibit potential anti-inflammatory effect in LPS stimulated RAW 264.7 cells.(In Vivo):Kaempferol-3-o-β-d-glucuronate exhibit potential anti-inflammatory effect in mice model.
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In Vitro——
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In Vivo——
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SynonymsKaempferol-3-beta-O-glucuronide | Kaempferol-3-glucuronide | Kaempferol-3-O-glucuronide
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PathwayApoptosis
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TargetIL Receptor
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RecptorIL Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number22688-78-4
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Formula Weight462.363
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Molecular FormulaC21H18O12
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (216.28 mM)
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SMILESO[C@H]1[C@H](Oc2c(oc3cc(O)cc(O)c3c2=O)-c2ccc(O)cc2)O[C@@H]([C@@H](O)[C@@H]1O)C(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
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Daclizumab
Daclizumab (Zenapax) is a humanized monoclonal antibody that specifically inhibits the alpha subunit of IL-2R-HA.
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