3''-Galloylquercitrin
1. 3''-Galloylquercitrin possesses the activity for PTK inhibition.
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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.
Sci Rep.2019, 9(1):6429
Front Plant Sci.2021, 12:673337.
Phytomedicine Plus2024, 4(4): 100655.
J Appl Toxicol.2020, 40(7):965-978.
Separations2023, 10(4), 231.
Environ Toxicol.2022, 37(3):514-526.
Phytochemistry Letters2017, 449-455
Environ Toxicol.2024, 39(4):2417-2428.
Mol Immunol. 2016, 78:121-132
Plant Direct.2021, 5(12):e372.
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J Asian Nat Prod Res. 2002 Dec;4(4):287-95.
Polyphenolic compounds from the leaves of Koelreuteria paniculata Laxm.[Pubmed:
12450257]
METHODS AND RESULTS:
From the fresh leaves of Koelreuteria paniculata Laxm (Sapindaceae), four new compounds, named ethyl p-trigallate (1), 3''-O-galloyl-4'-O-galloyl-4-O-galloyl-gallic acid (2), ethyl p-heptagallate (3) and 3''-Galloylquercitrin (4), together with 12 known compounds namely catechin (5), galloylepicatechin (6), isorhamnetin (7), kaempferol-3-O-arabinopyranoside (8), quercetin-3'-O-beta-D-arabinopyranoside (9), quercitrin (10), methyl p-digallate (11), methyl m-digallate (12), p-digalloyl acid (13), m-digalloyl acid (14), hyperin (15) and kaempferol-3-O-alpha-L-rhamnoside (16) were isolated by extensive column chromatographic separation.
CONCLUSIONS:
Their structures were elucidated on the basis of chemical and spectroscopic methods. Compound 9 was not reported previously with pyranoside of arabinose at C-3'. Compounds 4 and 9 possessed the activity for PTK inhibition.
