4'-O-Methyllicoflavanone

4'-O-Methyllicoflavanone
Product Name 4'-O-Methyllicoflavanone
CAS No.: 1038753-13-7
Catalog No.: CFN97958
Molecular Formula: C21H22O5
Molecular Weight: 354.4 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The herbs of Erythrina arborescens
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
4'-O-Methyllicoflavanone shows cytotoxic properties against P-388 cells, with the IC 50 value of 17.98 ug/mL.
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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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    CAS No: 1038753-13-7
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    Der Pharma Chemica, 2015 , 7 (1) :206-211.
    Phenolic compounds from the stem bark of Erythrina orientalis and their cytotoxic and antioxidant activities[Reference: WebLink]

    METHODS AND RESULTS:
    Two prenylated pterocarpans, phaseollin (1), shinpterocarpin (2) together with flavonoids, 4'-O-Methyllicoflavanone (3), alpinumisoflavone (4), 8-prenyl-daidzein (5), have been isolated from the stem bark of Erythrina orientalis. The structures of these compounds were determined based on UV, IR, HRESIMS, 1D and 2D NMR data.
    CONCLUSIONS:
    Compounds 1–5 were evaluated for their cytotoxic properties against P-388 cells, their IC 50 values 2.55, 2.43, 17.98, 4.31, and 5.82 μg/mL, respectively. Compounds 1, and 5 exhibited very high antioxidant activity against DPPH radical scavenging.
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