Norwogonin

Norwogonin
Product Name Norwogonin
CAS No.: 4443-09-8
Catalog No.: CFN92218
Molecular Formula: C15H10O5
Molecular Weight: 270.2 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Yellow powder
Targets: VHR
Source: The roots of Scutellaria baicalensis Georgi
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $318/20mg
Norwogonin(IC 50 = 1.1 microM) shows potent inhibitory activity toward VHR.
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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.
  • The Journal of Phytopharmacology2020, 9(1): 1-4
  • Int J Med Sci.2021, 18(10):2155-2161.
  • Appl. Sci. 2021, 11(8),3437.
  • Anal Bioanal Chem.2018, 410(5):1561-1569
  • Microb Biotechnol.2021, 14(5):2009-2024.
  • Microb Pathog.2024, 189:106609.
  • Antioxidants (Basel).2020, 9(2): E119
  • Environ Toxicol.2024, 39(5):2927-2936.
  • Molecules. 2013, 18(11):14105-21
  • J Physiol Biochem.2024, 80(2):421-437.
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    Biomol Ther (Seoul) . 2016 Sep 1;24(5):552-8.
    Inhibitory Effects of Norwogonin, Oroxylin A, and Mosloflavone on Enterovirus 71[Pubmed: 27257010]
    Abstract Severe complications associated with EV71 infections are a common cause of neonatal death. Lack of effective therapeutic agents for these infections underlines the importance of research for the development of new antiviral compounds. In the present study, the anti-EV71 activity of Norwogonin, oroxylin A, and mosloflavone from Scutellaria baicalensis Georgi was evaluated using a cytopathic effect (CPE) reduction method, which demonstrated that all three compounds possessed strong anti-EV71 activity and decreased the formation of visible CPEs. Norwogonin, oroxylin A, and mosloflavone also inhibited virus replication during the initial stage of virus infection, and they inhibited viral VP2 protein expression, thereby inhibiting viral capsid protein synthesis. However, ribavirin has a relatively weaker efficacy compared to the other drugs. Therefore, these findings provide important information that will aid in the utilization of Norwogonin, oroxylin A, and mosloflavone for EV71 treatment. Keywords: Antiviral activity; Enterovirus 71; Mosloflavone; Norwogonin; Oroxylin A.
    Planta Med. 2002 Dec;68(12):1063-5.
    Inhibition of VHR dual-specificity protein tyrosine phosphatase activity by flavonoids isolated from Scutellaria baicalensis: structure-activity relationships.[Pubmed: 12494330]
    Three flavonoids: Norwogonin, dihydroNorwogonin and baicalein, were isolated from the roots of Scutellaria baicalensis, as potential inhibitors of VHR dual-specificity protein tyrosine phosphatase (DS-PTPase).
    METHODS AND RESULTS:
    Norwogonin (IC 50 = 1.1 microM), dihydroNorwogonin (IC 50 = 2.9 microM) and baicalein (IC 50 = 2.4 microM) showed potent inhibitory activity toward VHR, but had no inhibitory activity against T-cell protein tyrosine phosphatase or serine/threonine protein phosphatase 1.
    CONCLUSIONS:
    From comparisons to the inhibitory activities of other similar flavonoids, it could be suggested that the presence of a hydroxy group in the B ring of flavonoids interferes with the inhibitory activity toward VHR DS-PTPase.
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