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    Natural Products
    Beta-Dimorphecolic acid (9(S)-HODE)
    Beta-Dimorphecolic acid (9(S)-HODE)
    Information
    CAS No. 18104-44-4 Price $318 / 5mg
    Catalog No.CFN95313Purity>=98%
    Molecular Weight296.5Type of CompoundLipids
    FormulaC18H32O3Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)  (SDF)
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    Address: No. 83, CheCheng Rd., WETDZ, Wuhan, Hubei 430056, PRC
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    * Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
    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 / $222.6 / In-stock
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
    Our products had been exported to the following research institutions and universities, And still growing.
  • Max Rubner-Institut (MRI) (Germany)
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  • Sri Ramachandra University (India)
  • Northeast Normal University Cha... (China)
  • University of Toulouse (France)
  • Siksha O Anusandhan University (India)
  • University of Vienna (Austria)
  • Univerzita Karlova v Praze (Czech Republic)
  • Kazusa DNA Research Institute (Japan)
  • University of British Columbia (Canada)
  • Melbourne University (Australia)
  • More...
  • Package
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    Beta-Dimorphecolic acid (9(S)-HODE)

    Beta-Dimorphecolic acid (9(S)-HODE)
    Product Name Beta-Dimorphecolic acid (9(S)-HODE)
    CAS No.: 18104-44-4
    Catalog No.: CFN95313
    Molecular Formula: C18H32O3
    Molecular Weight: 296.5 g/mol
    Purity: >=98%
    Type of Compound: Lipids
    Physical Desc.: Powder
    Source: The herbs of Piper cubeba
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $318 / 5mg
    Inquire / Order: manager@chemfaces.com
    Technical Inquiries: service@chemfaces.com
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  • Arch Toxicol.2017, 91(10):3225-3245
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    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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    Description: Anti-inflammatory activity.
    In vitro:
    Pharmacogn Mag . Jul-Sep 2015;11(43):477-85
    A direct protein kinase B-targeted anti-inflammatory activity of cordycepin from artificially cultured fruit body of Cordyceps militaris[Pubmed: 26246722]
    Background: Cordyceps militaris is one of well-known medicinal mushrooms with anti-inflammatory, anti-cancer, anti-diabetic, and anti-obesity activities. Objective: The objective of the following study is to isolate chemical components from the ethanol extract (Cm-EE) from Cordyceps militaris and to evaluate their anti-inflammatory activities. Materials and methods: Column chromatographic separation was performed and anti-inflammatory roles of these compounds were also examined by using NO production and protein kinase B (AKT) activity assays. Results: From Cm-EE, 13 constituents, including trehalose (1), cordycepin (2), 6-hydroxyethyladenosine (3), nicotinic amide (4), butyric acid (5), β-dimorphecolic acid (6), α-dimorphecolic acid (7), palmitic acid (8), linoleic acid (9), cordycepeptide A (10), 4-(2-hydroxy-3-((9E,12E)-octadeca-9,12-dienoyloxy)propoxy)-2-(trimethylammonio)butanoate (11), 4-(2-hydroxy-3-(palmitoyloxy)propoxy)-2-(trimethylammonio)butanoate (12), and linoleic acid methyl ester (13) were isolated. Of these components, compound 2 displayed a significant inhibitory effect on NO production in lipopolysaccharide (LPS)-activated RAW264.7 cells. Furthermore, this compound strongly and directly suppressed the kinase activity of AKT, an essential signalling enzyme in LPS-induced NO production, by interacting with its ATP binding site. Conclusion: C. militaris could have anti-inflammatory activity mediated by cordycepin-induced suppression of AKT.
    Beta-Dimorphecolic acid (9(S)-HODE) Description
    Source: The herbs of Piper cubeba
    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 3.3727 mL 16.8634 mL 33.7268 mL 67.4536 mL 84.317 mL
    5 mM 0.6745 mL 3.3727 mL 6.7454 mL 13.4907 mL 16.8634 mL
    10 mM 0.3373 mL 1.6863 mL 3.3727 mL 6.7454 mL 8.4317 mL
    50 mM 0.0675 mL 0.3373 mL 0.6745 mL 1.3491 mL 1.6863 mL
    100 mM 0.0337 mL 0.1686 mL 0.3373 mL 0.6745 mL 0.8432 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:
    ChemInform 63(32):7624-7633
    Enantioselective syntheses of (-)-pinellic acid, α- and β-dimorphecolic acid[Reference: WebLink]
    An efficient enantioselective convergent approach for the synthesis of (−)-pinellic acid 1, α- and β-dimorphecolic acid (2 and 3) from 1,9-nonane diol is described. The synthetic strategy features Sharpless asymmetric hydroxylation, Sonogashira coupling and Birch reduction.
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