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    Natural Products
    4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol
    4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol
    Information
    CAS No. 913643-31-9 Price $368 / 5mg
    Catalog No.CFN95200Purity>95%
    Molecular Weight346.4Type of CompoundPhenols
    FormulaC20H26O5Physical DescriptionSolid
    Download     COA    MSDSSimilar structuralComparison
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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 / $312.8 / In-stock
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    4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol

    4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol
    Product Name 4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol
    CAS No.: 913643-31-9
    Catalog No.: CFN95200
    Molecular Formula: C20H26O5
    Molecular Weight: 346.4 g/mol
    Purity: >95%
    Type of Compound: Phenols
    Physical Desc.: Solid
    Targets: HIV
    Source: The herbs of Schisandra propinqua
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $368 / 5mg
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  • In Vitro Cellular & Developmental Biology - Plant 2021, 57:874–882.
  • Molecules.2021, 26(4):817.
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  • Biomed Chromatogr.2020, e5021.
  • Universidade Estadual Paulista2017, 11449
  • Viruses.2017, 9(10)
  • TCI CO.2019, US20190151257A1
  • Front Pharmacol.2021, 12:607403.
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  • 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
  • Phenols Compound Library
  • HIV Inhibitor Library
  • Biological Activity
    Description: 4,4-di(4-Hydroxy-3-methoxyphenly)-2,3-dimethylbutanol has antioxidant and potential cytotoxic abilities, it also shows inhibition against HIV-1 integrase.
    Targets: HIV
    In vitro:
    Biol Res. 2009;42(3):351-6.
    Antioxidant isolated from Schisandra propinqua (Wall.) Baill.[Pubmed: 19915743 ]
    Schisandra propinqua (Wall.) Baill.(Schisandraceae) is widely used as a Chinese folk medicine.
    METHODS AND RESULTS:
    In this study, activity-guided fractionation of the ethanol extract from the stem of Schisandra propinqua led to the isolation of four extracts. Subsequently, a neolignan 4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol was isolated from the EtOAc part of the stem of Schisandra propinqua, the free radical scavenging activities of which were researched in vitro. The present work demonstrated that extracts and pure compound possessed scavenging activities to DPPH, superoxide anions and hydroxy radical, and could depress lipid peroxidation reaction induced by oxygen radical produced by the Fe2+/cysteine system in vitro.
    CONCLUSIONS:
    This suggests that the traditional application of Schisandra propinqua in China may be related to its antioxidant activities, and the EtOAc part of the stems of Schisandra propinqua can be utilized as an effective source of antioxidants.
    4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol Description
    Source: The herbs of Schisandra propinqua
    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.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.8868 mL 14.4342 mL 28.8684 mL 57.7367 mL 72.1709 mL
    5 mM 0.5774 mL 2.8868 mL 5.7737 mL 11.5473 mL 14.4342 mL
    10 mM 0.2887 mL 1.4434 mL 2.8868 mL 5.7737 mL 7.2171 mL
    50 mM 0.0577 mL 0.2887 mL 0.5774 mL 1.1547 mL 1.4434 mL
    100 mM 0.0289 mL 0.1443 mL 0.2887 mL 0.5774 mL 0.7217 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
    Kinase Assay:
    Yao Xue Xue Bao. 2010 Feb;45(2):235-40.
    Effective components against HIV-1 replicative enzymes isolated from plants.[Pubmed: 21351433]
    Plant active components characterized of many different structures and activities on multiple targets, have made them to be the important sources of inhibitors on HIV-1.
    METHODS AND RESULTS:
    For finding leading compounds with new structure against HIV-1, three key HIV-1 replicative enzymes (reverse transcriptase, protease and integrase) were used as screening models. The in vitro activities of 45 plant derived components isolated from Schisandraceae, Rutaceae and Ranunculaceae were reported. Within twelve triterpene components isolated, eight compounds were found to inhibit HIV-1 protease, in these eight active compounds, kadsuranic acid A (7) and nigranoic acid (8), inhibited both HIV-1 protease and integrase; Among fifteen lignans, meso-dihydroguaiaretic acid (15) and kadsurarin (16) were active on HIV-1 reverse transcriptase, and 4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol(13) active on HIV-1 integrase.
    CONCLUSIONS:
    All of the six alkaloids, seven flavones, and five others compounds were not active or only with low activities against HIV-1 replicative enzymes. Further studies of the triterpene components showing strong inhibitory activities on HIV-1 were warranted.
    Structure Identification:
    Journal of Integrative Plant Biology, 2006, 48(12):1493-1497.
    A Cytotoxic Neolignan from Schisandra propinqua (Wall.) Baill.[Reference: WebLink]
    In the course of our study of bioactive natural products from Schisandra plants, we isolated a neolignan from an EtOAc extract of the stems of Schisandra propinqua (Wall.) Baill.
    METHODS AND RESULTS:
    The structure of the new compound was determined to be 4,4-di(4-hydroxy-3-methoxyphenly)-2,3-dimethylbutanol(compound 1) on the basis of 1H- and 13C-NMR spectra and 2D NMR methods. Eight known compounds, compounds 2-9, were also isolated and identified, of which compounds 3, 4, 6 and 9 were isolated for the first time from this plant. In addition, compounds 1-4 were evaluated for cytotoxicity by an 3-(4,5-dimethyl-2 thiazoyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay.
    CONCLUSIONS:
    Compound 1 showed significant potential cytotoxic ability in the bioassay.
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