Anthraquinone
Reference standards.
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.
J.Acta Agriculturae Scandinavica2017, 571-575
Journal of Medicinal Food2023, Vol.26(10).
Patanjali Research Foundation2024, ssrn.4807357
J Liq Chromatogr R T2025, 2505536.
Arch Biochem Biophys.2020, 687:108384.
Inflammation.2022, 45(6):2529-2543.
Anal Sci.2019, 35(12):1317-1325
Front Immunol.2018, 9:2655
Int J Mol Sci.2022, 23(24):16000.
Molecules.2022, 27(7):2360.
Related and Featured Products
Applied & Environmental Microbiology, 1996, 62(12).
Oxidation of Anthracene and Benzo[a]pyrene by Laccases from Trametes versicolor.[Reference:
WebLink]
METHODS AND RESULTS:
The in vitro oxidation of the two polycyclic aromatic hydrocarbons anthracene and benzo[a]pyrene, which have ionization potentials of ≤7.45 eV, is catalyzed by laccases from Trametes versicolor. Crude laccase preparations were able to oxidize both anthracene and the potent carcinogen benzo[a]pyrene. Oxidation of benzo[a]pyrene was enhanced by the addition of the cooxidant 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonate) (ABTS), while an increased anthracene oxidizing ability was observed in the presence of the low-molecular-weight culture fluid ultrafiltrate. Two purified laccase isozymes from T. versicolor were found to have similar oxidative activities towards anthracene and benzo[a]pyrene. Oxidation of anthracene by the purified isozymes was enhanced in the presence of ABTS, while ABTS was essential for the oxidation of benzo[a]pyrene. In all cases Anthraquinone was identified as the major end product of anthracene oxidation.
CONCLUSIONS:
These findings indicate that laccases may have a role in the oxidation of polycyclic aromatic hydrocarbons by white rut fungi.
