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Quercetin 3-O-beta-(6-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside
Quercetin 3-O-beta-(6-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside
CAS No. 143061-65-8
Quercetin 3-O-beta-(6-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside( —— )
Catalog No. M31805 CAS No. 143061-65-8
Quercetin 3-O-β-D-(6''-p-coumaroyl)glucopyranosyl(1→2)-α-L-rhamnopyranoside is a compound extracted from the leaves of Ginkgo biloba.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 306 | In Stock |
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| 5MG | 215 | In Stock |
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| 10MG | 317 | In Stock |
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| 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 NameQuercetin 3-O-beta-(6-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside
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NoteResearch use only, not for human use.
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Brief DescriptionQuercetin 3-O-β-D-(6''-p-coumaroyl)glucopyranosyl(1→2)-α-L-rhamnopyranoside is a compound extracted from the leaves of Ginkgo biloba.
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DescriptionQuercetin 3-O-β-D-(6''-p-coumaroyl)glucopyranosyl(1→2)-α-L-rhamnopyranoside is a compound extracted from the leaves of Ginkgo biloba. Quercetin 3-o - -(6 '-p-coumaryl) glucopyranose (1->2) -α-L-rhamnoside has antioxidant properties.
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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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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number143061-65-8
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Formula Weight756.7
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Molecular FormulaC36H36O18
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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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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Xanthoangelol, which can be extracted from Angelica keiskei, inhibits obesity-induced inflammatory responses.Xanthoangelol has antimicrobial activity, inhibits monoamine oxidase, and induces apoptosis in neuroblastoma and leukemia cells.
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Maculosidin
Maculosidine affect the PS I electron acceptors on leaf discs, it can inhibit ATP synthesis, basal, phosphorylating and uncoupled electron transport acting as Hill reaction inhibitors on spinach chloroplasts.
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