Neophellamuretin
Neophellamuretin is a natural product from Akschindlium godefroyanum (Kuntze) H. Ohashi.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Journal of Ginseng Research2022, j.jgr.2022.09.005.
Food Chem.2023, 404(Pt A):134517.
Int J Mol Sci.2020, 21(19),7070.
VNU Journal of Science2023, 39(2):24-33.
Antioxidants (Basel).2021, 10(3):379.
Biomedicines.2021, 9(8):954.
Journal of Food and Drug Analysis2023, 31(3), 9.
J Appl Biol Chem2022, 65:343−348.
Environ Toxicol.2024, tox.24246
Int J Mol Sci.2022, 23(15):8687.
Related and Featured Products
Nat Prod Res. 2015;29(12):1177-9.
Radical scavenging activities of flavonoids from roots of Akschindlium godefroyanum.[Pubmed:
25426867 ]
METHODS AND RESULTS:
Chemical constituents of crude ethyl acetate extract of roots of Akschindlium godefroyanum (Kuntze) H. Ohashi were investigated and seven flavonoids were isolated. Their structures were identified based on spectroscopic methods as well as by comparison with spectral data reported in the literature as six flavanonols and a flavonol including 7,4'-dihydroxy-5,3'-dimethoxyflavanonol (1), Neophellamuretin (2), taxifolin (3), erycibenin D (4), geraldol (5), fustin (6) and garbanzol (7).
CONCLUSIONS:
Compounds 2, 4 and 7 were found in the genus Akschindlium for the first time. Compounds 3, 5 and 6 appeared to have free radical scavenging activities using DPPH assay with IC50 of 21, 40 and 15 μg/mL, respectively.
