Abiesinol F
Reference standards.
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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.
Phytother Res.2019, 33(4):1104-1113
Agronomy2023, 13(9), 2410.
Molecules.2019, 24(11):E2044
J.Food Processing & Preservation2022, jfpp.16666
Phytomedicine.2022, 100:154036.
Nat Prod Sci.2016, 22(2)
SCOPUS.2020, 836-847.
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Drug Des Devel Ther.2023, 17:2461-2479.
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Helvetica Chimica Acta, 2009, 92(8):1610-1620.
Flavonoids from Mirabilis himalaica.[Reference:
WebLink]
METHODS AND RESULTS:
Eight spiro-biflavonoids named abiesinol A, abiesinol B, abiesinol C, abiesinol D, abiesinol E, Abiesinol F, abiesinol G, abiesinol H, along with three neolignans, quercetin, and protocatechuic acid were isolated from the MeOH extract of the bark of Abies sachalinensis. The structures of these phenolic compounds were characterized by spectroscopic methods including NMR and MS.
CONCLUSIONS:
The absolute configurations of the abiesinols were determined by Mosher's method, CD, and NOESY data.
