7-Methoxyflavone

7-Methoxyflavone
Product Name 7-Methoxyflavone
CAS No.: 22395-22-8
Catalog No.: CFN70084
Molecular Formula: C16H12O3
Molecular Weight: 252.2 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The herbs of Zornia brasiliensis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $30/20mg
7-Methoxyflavone has peripheral antinociceptive 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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  • Exp Ther Med.2019, 18(6):4388-4396
  • Int J Med Sci.2021, 18(10):2155-2161.
  • J Clin Transl Hepatol.2023, 11(4):863-876.
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    Natural Product Letters, 2013, 27(18):1695-1699.
    Antinociceptive effect of 7-methoxyflavone isolated from Zornia brasiliensis.[Reference: WebLink]

    METHODS AND RESULTS:
    In this study, we investigated the antinociceptive effect of 7-Methoxyflavone (7MF) in mice using the following tests: acetic acid-induced writhing, glutamate- and formalin-induced nociception and hotplate. 7MF (30, 50, 100 and 300 μmol/kg, i.p.) reduced the number of writhes, with ID50 = 82.5 ± 11.7 μmol/kg and E max = 58.4%. 7MF treatment (100 μmol/kg, i.p.) inhibited paw-licking time in the neurogenic phase of the formalin pain response (65.6%) and did not decrease the nociceptive response in the inflammatory phase. In addition, in glutamate-induced nociception, 7MF inhibited 26% of the nociceptive answer. On the other hand, 7MF did not increase the latency time of the animals in the hotplate test.
    CONCLUSIONS:
    These results suggest that 7MF has peripheral antinociceptive activity.
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