Anthracophyllone
Anthracophyllone is a natural product from the mushroom Anthracophyllum sp. BCC18695.
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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 Korean Medicine2023, 44(4):26-40.
Natural Product Communications2020, doi: 10.1177.
Iranian Journal of Pharmaceutical Sciences2021, 17(2):25-36
Food Chem.2024, 458:140201.
Front Mol Neurosci.2023, 15:1083189.
Nat Prod Sci.2018, 24(3):206
Mol Neurobiol.2022, 02873-9.
J Korean Soc Food Sci Nutr2023, 52(12):1248-1255
Universite de Bordeaux2017, 2017BORD0867
The Journal of Supercritical Fluids2021, 176:105305.
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Phytochemistry Letters, 2013, 6(3):345-349.
Novel spiro-sesquiterpene from the mushroom Anthracophyllum sp. BCC18695.[Reference:
WebLink]
METHODS AND RESULTS:
A novel spiro-sesquiterpene, anthracophyllic acid (1), and a new aristolane sesquiterpene, Anthracophyllone (2), were isolated from the mushroom Anthracophyllum sp. BCC18695, together with seven known compounds including aurisins A (3), G (4), K (5), nambinones A, C, axinysones A, and B. The relative configuration of 1 and the hitherto unknown absolute stereochemistry of 3 were determined based on X-ray spectroscopic data.
CONCLUSIONS:
Biological activities including antimalarial activity against Plasmodium falciparum K1 strain, antibacterial property against Bacillus cereus, and cytotoxicity against MCF-7, KB, NCI-H187, and Vero cells of the isolated compounds were also evaluated
