1,4,5,6-Tetrahydroxy-7-prenylxanthone
1,4,5,6-Tetrahydroxy-7-prenylxanthone has anti-cancer activity, it shows moderate cytotoxicities against breast cancer (MDA-MB-435S) and lung adenocarcinoma (A549) cell lines; it also exhibits moderate activities with GI50 (Growth inhibitory) values of 2.8 μM against the human leukaemic HL-60 cell line were measured in vitro.
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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.
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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.
VNU J Science: Med.&Pharm. Sci.2024.2588-1132
Journal of Natural Remedies2024, 24(3):555¨C575.
Nutrients.2020, 12(3):595.
BMC Plant Biol.2023, 23(1):239.
Int. J. Mol. Sci.2023, 24(20),15294.
Food Chem.2017, 221:1135-1144
Antioxidants (Basel).2020, 9(2): E119
Biomed Chromatogr.2020, e5021.
BMC Plant Biol.2018, 18(1):122
Pharmaceuticals (Basel).2022, 15(5):591.
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Phytochemistry. 2009 Jan;70(1):60-8.
Xanthone biosynthesis in Hypericum perforatum cells provides antioxidant and antimicrobial protection upon biotic stress.[Pubmed:
19062051 ]
METHODS AND RESULTS:
Methanolic extract of elicited cells exhibited significantly higher antioxidant and antimicrobial competence than the equivalent extract of control HP cells indicating that these properties have been significantly increased in HP cells after elicitation. Four major de novo synthesized xanthones have been identified as 1,3,6,7-tetrahydroxy-8-prenyl xanthone(1,4,5,6-Tetrahydroxy-7-prenylxanthone), 1,3,6,7-tetrahydroxy-2-prenyl xanthone, 1,3,7-trihydroxy-6-methoxy-8-prenyl xanthone and paxanthone.
CONCLUSIONS:
Antioxidant and antimicrobial characterization of these de novo xanthones have revealed that xanthones play dual function in plant cells during biotic stress: (1) as antioxidants to protect the cells from oxidative damage and (2) as phytoalexins to impair the pathogen growth.
