Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside [Quercetin-3-O-(2G-alpha-L-rhamnosyl)-rutinoside]
Quercetin 3-O-rutinoside-(1→2)-O-rhamnoside shows α-glucosidase inhibitory activity, it has anti-diabetic potential.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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
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.
Food Chem.2021, 360:130063.
Microchemical Journal2014, 203:110804.
Talanta Open2023, 7:100227
BMC Plant Biol.2023, 23(1):239.
Biomedicines.2022, 10(2):463.
Front Cell Dev Biol.2021, 9:588093.
Asian Journal of Chemistry2014, 26(8):2425
BMC Microbiol.2019, 19(1):78
J Ethnopharmacol.2016, 194:219-227
J Ethnopharmacol.2019, 241:112025
Related and Featured Products
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]](https://www.chemfaces.com/structural/Quercetin-3-O-rutinoside-1-2-O-rhamnoside-CFN91149.jpg "Quercetin 3-O-rutinoside-(1->2)-O-rhamnoside [Quercetin-3-O-(2G-alpha-L-rhamnosyl)-rutinoside]")
