Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside [Quercetin-3-O-(2G-alpha-L-rhamnosyl)-rutinoside] | CAS:55696-57-6

Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside [Quercetin-3-O-(2G-alpha-L-rhamnosyl)-rutinoside]

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Product Name	Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside [Quercetin-3-O-(2G-alpha-L-rhamnosyl)-rutinoside]
Price:	$318 / 10mg
CAS No.:	55696-57-6
Catalog No.:	CFN91149
Molecular Formula:	C₃₃H₄₀O₂₀
Molecular Weight:	756.7 g/mol
Purity:	>=98%
Type of Compound:	Flavonoids
Physical Desc.:	Powder
Source:	The herbs of Callicarpa bodinieri
Solvent:	DMSO, Pyridine, Methanol, Ethanol, etc.
Download:	COA MSDS
Similar structural:	Comparison
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.

Size /Price /Stock	10 mM * 1 mL in DMSO / $230.5 / In-stock
Other Packaging	*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap

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Description:

Quercetin 3-O-rutinoside-(1→2)-O-rhamnoside shows α-glucosidase inhibitory activity, it has anti-diabetic potential.

Targets:

α-glucosidase

In vitro:

Food Chem. 2019 Jun 1;282:9-17.

Comprehensive structural characterization of phenolics in litchi pulp using tandem mass spectral molecular networking.[Pubmed: 30711110 ]

Phenolic compounds are a large class of plant secondary metabolites with various health-promoting effects, and are known for their structural diversity. Therefore, high efficiency characterization of phenolic profiles is of key importance in identifying their potential bioactivity.
METHODS AND RESULTS:
In the present study, Global Natural Products Social (GNPS) Molecular Networking was applied to trace the phenolic compounds in plants, which allowed the characterization of 9 procyanidins and 11 flavonoid glycosides (di-, tri-, or tetra-saccharides of kaempferol, quercetin, isorhamnetin and myricetin) in litchi pulp extracts.
CONCLUSIONS:
Six compounds were reported for the first time in litchi pulp. In addition, Quercetin 3-O-rutinoside-(1→2)-O-rhamnoside, the most abundant flavonoid glycoside in litchi pulp, was proved to have considerable α-glucosidase inhibitory activity, illustrating the anti-diabetic potential of phenolic-rich litchi pulp extracts.

Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside [Quercetin-3-O-(2G-alpha-L-rhamnosyl)-rutinoside] Description

Source:	The herbs of Callicarpa bodinieri
Solvent:	DMSO, Pyridine, Methanol, Ethanol, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Flavonoids Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	1.3215 mL	6.6076 mL	13.2153 mL	26.4306 mL	33.0382 mL
5 mM	0.2643 mL	1.3215 mL	2.6431 mL	5.2861 mL	6.6076 mL
10 mM	0.1322 mL	0.6608 mL	1.3215 mL	2.6431 mL	3.3038 mL
50 mM	0.0264 mL	0.1322 mL	0.2643 mL	0.5286 mL	0.6608 mL
100 mM	0.0132 mL	0.0661 mL	0.1322 mL	0.2643 mL	0.3304 mL

CFN90691	9'-Methyl lithospermate B	1167424-31-8	732.64	C₃₇H₃₂O₁₆
CFN90614	17-Hydroxy sprengerinin C	1029017-75-1	871.02	C₄₄H₇₀O₁₇
CFN99327	Scutebata G	1207181-63-2	679.8	C₄₀H₄₁NO₉
CFN93314	Topotecan	123948-87-8	421.45	C₂₃H₂₃N₃O₅