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3''-Galloylquercitrin
3''-Galloylquercitrin
Information
CAS No. 503446-90-0 Price $368 / 5mg
Catalog No.CFN95048Purity>=98%
Molecular Weight600.5Type of CompoundFlavonoids
FormulaC28H24O15Physical DescriptionYellow powder
Download COA    MSDSSimilar structuralComparison
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Size /Price /Stock 10 mM * 1 mL in DMSO / $478.4 / In-stock
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    3''-Galloylquercitrin

    3''-Galloylquercitrin
    Product Name 3''-Galloylquercitrin
    CAS No.: 503446-90-0
    Catalog No.: CFN95048
    Molecular Formula: C28H24O15
    Molecular Weight: 600.5 g/mol
    Purity: >=98%
    Type of Compound: Flavonoids
    Physical Desc.: Yellow powder
    Source: The herbs of Polygonum capitatum
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Price: $368 / 5mg
    Download: COA    MSDS
    Similar structural: Comparison
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    product package
  • FEBS J.2022, 10.1111:febs.16676.
  • Nutrients2022, 14(14)2929
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  • Drug Dev Res.2022, 83(7):1673-1682.
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  • Heliyon.2023, e12778.
  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
    Related Libraries
    Biological Activity
    Description: 1. 3''-Galloylquercitrin possesses the activity for PTK inhibition.
    3''-Galloylquercitrin Description
    Source: The herbs of Polygonum capitatum
    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.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.6653 mL 8.3264 mL 16.6528 mL 33.3056 mL 41.632 mL
    5 mM 0.3331 mL 1.6653 mL 3.3306 mL 6.6611 mL 8.3264 mL
    10 mM 0.1665 mL 0.8326 mL 1.6653 mL 3.3306 mL 4.1632 mL
    50 mM 0.0333 mL 0.1665 mL 0.3331 mL 0.6661 mL 0.8326 mL
    100 mM 0.0167 mL 0.0833 mL 0.1665 mL 0.3331 mL 0.4163 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Structure Identification:
    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.
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