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    Lupeol 3-hydroxyoctadecanoate
    Lupeol 3-hydroxyoctadecanoate
    CAS No. 108885-61-6 Price
    Catalog No.CFN96396Purity>=98%
    Molecular Weight709.2Type of CompoundTriterpenoids
    FormulaC48H84O3Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)
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    Lupeol 3-hydroxyoctadecanoate Description
    Source: The roots of Biondia hemsleyana.
    Biological Activity or Inhibitors:
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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.
    Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.

    PMID: 29328914

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.

    PMID: 29149595

    Scientific Reports 2017 Dec 11;7(1):17332.
    doi: 10.1038/s41598-017-17427-6.

    PMID: 29230013

    Molecules. 2017 Oct 27;22(11). pii: E1829.
    doi: 10.3390/molecules22111829.

    PMID: 29077044

    J Cell Biochem. 2018 Feb;119(2):2231-2239.
    doi: 10.1002/jcb.26385.

    PMID: 28857247

    Phytomedicine. 2018 Feb 1;40:37-47.

    PMID: 29496173
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.41 mL 7.0502 mL 14.1004 mL 28.2008 mL 35.251 mL
    5 mM 0.282 mL 1.41 mL 2.8201 mL 5.6402 mL 7.0502 mL
    10 mM 0.141 mL 0.705 mL 1.41 mL 2.8201 mL 3.5251 mL
    50 mM 0.0282 mL 0.141 mL 0.282 mL 0.564 mL 0.705 mL
    100 mM 0.0141 mL 0.0705 mL 0.141 mL 0.282 mL 0.3525 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.
    Lupeol 3-hydroxyoctadecanoate References Information
    Citation [1]

    Chemical Research in Chinese Universities,2003,24(3):436-41.

    Chemical Constituents from the Roots of Biondia Hemsleyana[Reference: WebLink]
    Nineteen I compounds were isolated from the,ethanol extract of the roots of Biondia hemsleyana (Warb.) Tsiang through. the repeated column chromatography on normal and reversed phase silica gel. By the spectroscopic and chemical evidence, their structures were elucidated as alpha-amyrin-3beta-acetate (1), Lupeol 3-hydroxyoctadecanoate (2), lupeol 3, 5-dihydroxyeicosanoate (3), cycloeucalenol (4), 4-methoxy salicylic aldehyde(5), 4-methoxy salicylic acid(6), isovanillin(7), scopoletin(8), isovanillic acid(9), cleomiscosin A (10), 2-hydroxmethyl-5-methoxylphenyl-O-beta-D-glucopyranoside (11), pregn-4-ene-3, 20-dione (12), neridienone (13), daucosterol(14), pregn-5-ene-3beta, 17alpha, 20alpha-triol-20-O-beta-D-canaropyranoside (15), periplogenin-3-O-beta-D-gluco pyranosyl-(1-->4)-beta-D-cymaropyranoside (16), pregn-5-ene-3beta, 20 (S)-diol-3-O-[2-O-acetyl-beta-D-digitalopyranosyl (1-->4)-beta-D-cymaropyranosyl]-20-O-beta-D-glucopyranosyl-(1-->6)-beta- D-glucopyranosyl-(1-->4)-beta-D-digitalo pyranoside(17), pregn-5-ene-3beta, 20(S)-diol-20-O-alpha-D-glucopyranosyl-(1-->6)-beta-D-glucopyranoside(18 , biondianoside C) and pregn-5-ene-3beta, 20(S)-diol-3-O-[beta-D-glucopyranosyl]-20-O-beta-D-glucopyranosyl-(1-->6 )-beta-D-glucopyranoside (19, biondianoside D) respectively. All compounds were isolated from this genus for the first time and 3, 11, 18 and 19 were new compounds among them.