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    Scutebarbatine W
    Scutebarbatine W
    Information
    CAS No. 1312716-25-8 Price
    Catalog No.CFN96705Purity>=98%
    Molecular Weight575.65Type of CompoundDiterpenoids
    FormulaC33H37NO8Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison
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    Scutebarbatine W Description
    Source: The whole plants of Scutellaria barbata.
    Biological Activity or Inhibitors: 1. Scutebarbatine W can inhibit nitric oxide production efficiently with IC50 values of lower than 50 uM, it may have potential effects on the reduction of neuroinflammation.
    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.
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.7372 mL 8.6858 mL 17.3717 mL 34.7433 mL 43.4292 mL
    5 mM 0.3474 mL 1.7372 mL 3.4743 mL 6.9487 mL 8.6858 mL
    10 mM 0.1737 mL 0.8686 mL 1.7372 mL 3.4743 mL 4.3429 mL
    50 mM 0.0347 mL 0.1737 mL 0.3474 mL 0.6949 mL 0.8686 mL
    100 mM 0.0174 mL 0.0869 mL 0.1737 mL 0.3474 mL 0.4343 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.
    Scutebarbatine W References Information
    Citation [1]

    Chem Pharm Bull (Tokyo). 2010 Sep;58(9):1267-70.

    Scutebarbatines W-Z, new neo-clerodane diterpenoids from Scutellaria barbata and structure revision of a series of 13-spiro neo-clerodanes.[Pubmed: 20823615]
    Four new neo-clerodane diterpenoids, Scutebarbatine W, scutebarbatine X, scutebarbatine Y, scutebarbatine Z (1-4), were isolated from the ethanol extract of Scutellaria barbata (Labiatae), and their structures were elucidated on the basis of extensive spectroscopic studies. In addition, the proposed structures of at least seven 13-spiro subtype neo-clerodanes: scutehenanine B (5), scutebarbatine G (6), 6-O-nicotinoylscutebarbatine G (7), barbatin A (8), 6,7-di-O-nicotinoylscutebarbatine G (9), 6-O-nicotinoyl-7-O-acetylscutebarbatine G (10), and scutebarbatine F (11), reported by Dai and co-workers from the same species, were incorrectly assigned and have been revised by reanalysis of the published NMR data.
    Citation [2]

    Chem. Biodivers.,2017 Aug 14.

    Constituents from Scutellaria barbata Inhibiting Nitric Oxide Production in LPS-stimulated Microglial Cells.[Pubmed: 28805952]
    The arial parts of Scutellaria barbata D. Don (Lamiaceae) efficiently inhibited NO production in BV2 microglial cells, and the active constituents were further isolated based on activity-guided isolation using silica-gel column chromatography, RP-C18 MPLC and prep-HPLC. As the results, 2 flavonoids including 6-methoxynaringenin (1) and 6-O-methylscutellarein (5), and 6 neo-clerodane diterpenes such as Scutebarbatine W (2), scutebatas B (3), scutebarbatine B (4), scutebarbatine A (6), 6-O-nicotinolylscutebarbatine G (7) and Scutebarbatine X (8) were isolated. The structures of these compounds were elucidated based on NMR and MS data, and the comparison of literature values. All the compounds except compound 7 inhibited NO production efficiently with IC50 values of lower than 50 μM. Particularly, compound 1 and 8 were the most efficient with IC50 values of 25.8 and 27.4 μM, respectively. This is the first report suggesting the potential of S. barbata on the reduction of neuroinflammation.