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    Natural Products
    Dehydrogeijerin
    Information
    CAS No. 16850-91-2 Price
    Catalog No.CFN89248Purity>=98%
    Molecular Weight258.27Type of CompoundCoumarins
    FormulaC15H14O4Physical DescriptionPowder
    Download COA    MSDSSimilar structuralComparison (Web)  (SDF)
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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 / Inquiry
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    Dehydrogeijerin

    Dehydrogeijerin
    Product Name Dehydrogeijerin
    CAS No.: 16850-91-2
    Catalog No.: CFN89248
    Molecular Formula: C15H14O4
    Molecular Weight: 258.27 g/mol
    Purity: >=98%
    Type of Compound: Coumarins
    Physical Desc.: Powder
    Targets: NO | COX | NOS | MAPK
    Source: The roots of Angelica dahurica var. formosana cv. Chuanbaizhi.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price:
    Download: COA    MSDS
    Similar structural: Comparison (Web)  (SDF)
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  • Chemistry of Plant Materials.2019, 129-136
  • Anat Rec2018, 24264
  • Front Pharmacol.2020, 11:251.
  • J Anal Methods Chem.2022, 2022:2229500.
  • J of Advanced Scientific R.2020, 11(3), p109-120.
  • Korean Journal of Pharmacognosy2017, 48(4):320-328
  • Cell Biochem Funct.2018, 36(6):303-311
  • Int J Mol Sci.2021, 22(19):10405.
  • Molecules.2019, 24(6):E1177
  • Biomed Pharmacother.2019, 111:262-269
  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
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  • Biological Activity
    Description: Dehydrogeijerin significantly inhibits the inflammatory activity of activated macrophages, suggesting that it could be a potential candidate for the treatment of inflammatory disease.
    Targets: NO | COX | NOS | MAPK
    In vitro:
    Int Immunopharmacol. 2012 Dec;14(4):734-9.
    Anti-inflammatory effects of dehydrogeijerin in LPS-stimulated murine macrophages.[Pubmed: 23102664]

    METHODS AND RESULTS:
    In this study, we investigated whether Heracleum (H) moellendorffii Hance-derived Dehydrogeijerin and geijerin could be used to suppress lipopolysaccharide (LPS)-induced inflammatory responses in murine macrophage cell lines, Raw 264.7 cells. Dehydrogeijerin reduced nitric oxide (NO) and inducible nitric oxide synthase (iNOS) production from LPS-stimulated Raw 264.7 cells, but on the other hand, geijerin did not reduce NO production. Dehydrogeijerin, unlike geijerin, has a double bond at C2'-C3' with an oxo function at C1'. Pre-treatment of Raw 264.7 cells with Dehydrogeijerin reduced the production of cyclooxigenase-2 (COX-2) and pro-inflammatory cytokines. These inhibitory effects were associated with decreases in the phosphorylation of mitogen-activated protein (MAP) kinases.
    CONCLUSIONS:
    Our results indicate that Dehydrogeijerin significantly inhibits the inflammatory activity of activated macrophages, suggesting that Dehydrogeijerin could be a potential candidate for the treatment of inflammatory disease.
    Dehydrogeijerin Description
    Source: The roots of Angelica dahurica var. formosana cv. Chuanbaizhi.
    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 3.8719 mL 19.3596 mL 38.7192 mL 77.4383 mL 96.7979 mL
    5 mM 0.7744 mL 3.8719 mL 7.7438 mL 15.4877 mL 19.3596 mL
    10 mM 0.3872 mL 1.936 mL 3.8719 mL 7.7438 mL 9.6798 mL
    50 mM 0.0774 mL 0.3872 mL 0.7744 mL 1.5488 mL 1.936 mL
    100 mM 0.0387 mL 0.1936 mL 0.3872 mL 0.7744 mL 0.968 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:
    Zhongguo Zhong Yao Za Zhi. 2015 Jun;40(11):2148-56.
    Chemical constituents from lipophilic parts in roots of Angelica dahurica var. formosana cv. Chuanbaizhi.[Pubmed: 26552172]
    The chemical constituents from lipophilic parts in the roots of Angelica dahurica var. formosana cv. Chuanbaizhi were studied in this paper.
    METHODS AND RESULTS:
    The compounds were separated and purified by repeated column chromatographic methods on silica gel and HPLC, and the chemical structures of compounds were determined by spectral data analyses. Twenty-nine compounds were obtained and identified as isoimperatorin (1), β-sitosterol (2), imperatorin (3), bergapten (4), osthenol (5), xanthotoxin (6), isoimpinellin (7), Dehydrogeijerin (8), phellopterin (9), isodemethylfuropinarine (10), 7-demethylsuberosin (11), alloimperatorin (12), xanthotoxol (13), isooxypeucedanin (14), alloisoimperatorin (15), demethylfuropinarine (16), 5-hydroxy-8-methoxypsoralen (17), oxypeucedanin methanolate (18), pabulenol (19), byakangelicin (20), marmesin (21), (+) -decursinol (22), heraclenol (23), oxypeucedanin hydrate (24), marmesinin (25), ulopterol (26), erythro-guaiacylglycerol-β-ferulic acid ether (27), threo-guaiacylglycerol-β-ferulic acid ether (28), and uracil (29).
    CONCLUSIONS:
    Compounds 5, 8, 11, 18, 21-23, and 26-28 were obtained from the roots of title plant for the first time.
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