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    Natural Products
    CAS No. 11088-09-8 Price $268 / 10mg
    Catalog No.CFN99207Purity>=98%
    Molecular Weight867.9 Type of CompoundSesquiterpenoids
    FormulaC43H49NO18Physical DescriptionPowder
    Download Manual    COA    MSDS    SDFSimilar 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 / $202.7 / In-stock
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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    Product Name Wilforine
    CAS No.: 11088-09-8
    Catalog No.: CFN99207
    Molecular Formula: C43H49NO18
    Molecular Weight: 867.9 g/mol
    Purity: >=98%
    Type of Compound: Sesquiterpenoids
    Physical Desc.: Powder
    Targets: TNF-伪 | IL Receptor | NO | ATPase | Sodium channel | Potassium channel
    Source: The vines of Tripterygium wilfordii.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $268 / 10mg
    Inquire / Order:
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    Tel: +86-27-84237783
    Fax: +86-27-84254680

    1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
  • Oncotarget.2017, 8(64):108006-108019
  • Journal of Apiculture2019, 34(2):131-136
  • Molecules 2022, 27(3),1047.
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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
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  • Biological Activity
    Description: Wilforine has anti-inflammatory effect, which might be mediated by down-regulation of the expression of inflammatory factors TNF-α, IL-6 and NO. It also has insecticidal activity by inhibiting the Na+-K+-ATPase in the central nervous system.
    Targets: TNF-α | IL Receptor | NO | ATPase | Sodium channel | Potassium channel
    In vitro:
    J Microbiol Biotechnol. 2014 Jun 28;24(6):823-34.
    Establishment of Tripterygium wilfordii Hook. f. Hairy root culture and optimization of its culture conditions for the production of triptolide and wilforine.[Pubmed: 24651642]

    In order to solve the shortage of natural Tripterygium wilfordii Hook. f. plant resource for the production of the important secondary metabolites triptolide and Wilforine, hairy roots were induced from its root calli by Agrobacterium rhizogenes. Induced hairy roots not only could be maintained and grown well in hormone-free half-strength Murashige and Skoog medium but also could produce sufficient amounts of both triptolide and Wilforine. Although hairy roots produced approximately 15% less triptolide than adventitious roots and 10% less Wilforine than naturally grown roots, they could grow fast and could be a suitable system for producing both secondary metabolites compared with other tissues. Addition of 50 micrometer methyl jasmonate (MeJA) could slightly affect hairy root growth, but dramatically stimulated the production of both triptolide and Wilforine, whereas 50 micrometer salicylic acid had no apparent effect on hairy root growth with slightly stimulatory effects on the production of both secondary metabolites. Addition of precursor nicotinic acid, isoleucine, or aspartic acid at the concentration of 500 micrometer had varying effects on hairy root growth, but none of them had stimulatory effects on triptolide production, and only the former two had slightly beneficial effects on Wilforine production. The majority of triptolide produced was secreted into the medium, whereas most of the produced Wilforine was retained inside of hairy roots.
    Our studies provide a promising way to produce triptolide and Wilforine in T. wilfordii hairy root cultures combined with MeJA treatment.
    Wilforine Description
    Source: The vines of Tripterygium wilfordii.
    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:

    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 1.1522 mL 5.761 mL 11.5221 mL 23.0441 mL 28.8052 mL
    5 mM 0.2304 mL 1.1522 mL 2.3044 mL 4.6088 mL 5.761 mL
    10 mM 0.1152 mL 0.5761 mL 1.1522 mL 2.3044 mL 2.8805 mL
    50 mM 0.023 mL 0.1152 mL 0.2304 mL 0.4609 mL 0.5761 mL
    100 mM 0.0115 mL 0.0576 mL 0.1152 mL 0.2304 mL 0.2881 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.
    Structure Identification:
    Biomed Chromatogr. 2015 Jul;29(7):1042-7.
    Application of a sensitive and specific LC-MS/MS method for determination of wilforine from Tripterygium wilfordii Hook. F. in rat plasma for a bioavailability study.[Pubmed: 25425175]

    A highly selective and specific LC-MS/MS method was developed and validated for the determination of Wilforine in rat plasma. The analyte was separated from plasma matrix by using methyl tertiary butyl ether liquid-liquid extraction with bulleyacinitine A as internal standard (IS). The analysis was carried out on a Sepax GP-Phenyl column using a mixture of methanol and 10 mmol/L ammonium formate buffer solution containing 0.1% formic acid (75:25, v/v) as the mobile phase pumped at a flow rate of 1.0 mL/min. The detection was operated using a triple-quadrupole mass spectrometer in multiple selected reaction monitoring with the parent-to-product quantifier transitions [M + H]+ m/z 867.6 →206.0 for Wilforine and 664.1 →584.1 for IS. The main advantage of this method was the high sensitivity (a lower limit of quantification of 0.02 ng/mL) and the small amount of sample (0.1 mL plasma per sample).
    The method was fully validated to be accurate and precise with a linear range of 0.02-100 ng/mL, and successfully applied to a bioavailability study of Wilforine in rats after intravenous and oral administration. The oral absolute bioavailability of Wilforine in rats was estimated to be 84%.

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