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Luteolin-4-O-glucoside
CAS No. 6920-38-3
Luteolin-4-O-glucoside ( —— )
Catalog No. M25048 CAS No. 6920-38-3
Luteolin-4'-O-glucoside is an IL-5 inhibitor with an IC50 of 3.7 μM. Luteolin-4'-O-glucoside resists hyperuricemia and acute gouty arthritis activity. Luteolin-4'-O-glucoside shows anticancer activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 1044 | In Stock |
|
| 10MG | 1404 | In Stock |
|
| 25MG | 2088 | In Stock |
|
| 50MG | 2808 | 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 NameLuteolin-4-O-glucoside
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NoteResearch use only, not for human use.
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Brief DescriptionLuteolin-4'-O-glucoside is an IL-5 inhibitor with an IC50 of 3.7 μM. Luteolin-4'-O-glucoside resists hyperuricemia and acute gouty arthritis activity. Luteolin-4'-O-glucoside shows anticancer activity.
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DescriptionLuteolin-4'-O-glucoside is an IL-5 inhibitor with an IC50 of 3.7 μM. Luteolin-4'-O-glucoside resists hyperuricemia and acute gouty arthritis activity. Luteolin-4'-O-glucoside shows anticancer activity.Luteolin-4'-O-glucoside shows cytotoxic activity against NCI-H929, U266, and OPM2 cell lines.
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In VitroLuteolin-4'-O-glucoside shows cytotoxic activity against NCI-H929, U266, and OPM2 cell lines.
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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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RecptorIL-5
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Research Area——
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Indication——
Chemical Information
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CAS Number6920-38-3
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Formula Weight448.38
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Molecular FormulaC21H20O11
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C1C(C(OC(C(C=C2)=CC(O)=C2O[C@@H]([C@@H]([C@H]3O)O)O[C@@H]([C@H]3O)CO)=C1)=CC(O)=C4)=C4O
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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. Park KY, et al. Inhibitory effect of luteolin 4'-O-glucoside from Kummerowia striata and other flavonoids on interleukin-5 bioactivity. Planta Med. 1999 Jun;65(5):457-9.
2. Xu T, et al. Glycosylation of luteolin in hydrophilic organic solvents and structure–antioxidant relationships of luteolin glycosides. RSC Advances, 2022, 12(28): 18232-18237.
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