83048-35-5
Chemical Structure
Quercetin 3-O-sambubioside
- CAS No.: 83048-35-5
- Formula:C26H28O16
- Molecular Weight:596.49
IUPAC Name: 3-(((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one
InChIKey: NKFZLEYLWAFYEH-CJNLAGEVSA-N
SMILES: O=C1C(O[C@H](O[C@@H]2CO)[C@@H]([C@H]([C@@H]2O)O)O[C@H](OC[C@H]3O)[C@@H]([C@H]3O)O)=C(C(C=C4)=CC(O)=C4O)OC5=CC(O)=CC(O)=C15
Biological Activity: Quercetin-3-O-sambubioside is a monomeric compound found in Eucommia ulmoides male flowers. Quercetin-3-O-sambubioside promotes the stimulation of the nerve center. Antioxidant and anticancer activities[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Quercetin 3-O-sambubioside | 98.76% | Quercetin-3-O-sambubioside is a monomeric compound found in Eucommia ulmoides male flowers. Quercetin-3-O-sambubioside promotes the stimulation of the nerve center. Antioxidant and anticancer activities. | ||||||||||||||||||||
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Similarity Score 1.00
HY-N17847Quercetin-3-O-β-D-xylosyl-(1→2)-β-D-galactoside -
Similarity Score 0.92
HY-N13734Quercitrin 2''-O-arabinoside -
Similarity Score 0.91
HY-N12862Floramanoside A -
Similarity Score 0.91
HY-N7907Myricetin-3-O-β-D-xylopyranosyl-(1→2)-β-D-glucopyranoside -
Similarity Score 0.90
HY-N7976Quercetin 3-O-neohesperidoside -
Similarity Score 0.90
HY-N11655Antioxidant agent-10 -
Similarity Score 0.90
HY-N11808Quercetin 3-galactosyl(1→2)rhamnoside -
Similarity Score 0.90
![Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnoside Chemical Structure](//file.medchemexpress.com/product_pic/hy-n7607.gif)
HY-N7607Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnoside -
Similarity Score 0.89
HY-N2186RLeucoside (Standard) -
Explore the MedChemAI to find more analogs
![Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnoside Chemical Structure](http://file.medchemexpress.com/product_pic/hy-n7607.gif)
References
- [1]. Li X, et al. Effect of quercetin-3-O-sambubioside isolated from Eucommia ulmoides male flowers on spontaneous activity and convulsion rate in mice. Planta Med. 2014;80(12):974-977. [Content Brief]
- [2]. Bao Chen, et al. Application of high‐speed counter‐current chromatography and HPLC to separate and purify of three polyacetylenes from Platycodon grandiflorum. SHORT COMMUNICATION.
