Futoenone

Futoenone
Product Name Futoenone
CAS No.: 19913-01-0
Catalog No.: CFN96370
Molecular Formula: C20H20O5
Molecular Weight: 340.4 g/mol
Purity: >=98%
Type of Compound: Lignans
Physical Desc.: Powder
Targets: PAFR
Source: The stems of Piper kadsura.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Futoenone and a series of its derivatives have shown inhibitory activities against matrix metalloproteinases, the molecular modelings of these compounds indicate the preferred binding of the P2′ site of the enzymes. Neolignan derivative compounds of the 2,4-diaryl-1,3-dithiolane and futoenone variety exhibit both platelet activating factor receptor(PAF)and 5-lipoxygenase antagonist activity.
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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

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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    The Journal of Chinese medicine,2002,13(3):159-70.
    Some Immunomodulatory Principles Isolated from Piper Kadsura[Reference: WebLink]

    METHODS AND RESULTS:
    From the ethanol extract of the stem of Piper kadsura (Piperaceae), seven compounds-futoquinol; Futoenone; (+)-crotepoxide; galgravin; (-)galbelgin; piperlactam S and piperolactam B were isolated, identified and tested for immunopharmacological activities with human mononuclear cells (HMNC) being used as target cells and cell proliferation determined by 3Hthymidine uptake.
    CONCLUSIONS:
    The results indicated that compounds futoquinol, galgravin, piperlactam S and piperolactam B potently inhibited HMNC proliferation and interferon-g production. Therefore immunosup pressive mechanisms might involve the impairment of cytokines production.
    Bioorganic & Medicinal Chemistry Letters,1995,5(15):1637-42.
    Inhibition of metalloproteinase by futoenone derivatives[Reference: WebLink]

    METHODS AND RESULTS:
    Futoenone and a series of its derivatives have shown inhibitory activities against matrix metalloproteinases. The molecular modelings of these compounds indicate the preferred binding of the P2′ site of the enzymes.
    EP 0574510 A4[P].1994.
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    METHODS AND RESULTS:
    Neolignan derivative compounds of the 2,4-diaryl-1,3-dithiolane and Futoenone variety exhibit both PAF and 5-lipoxygenase antagonist activity.
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