6-epi-Albrassitriol
6-epi-Albrassitriol is a natural product from A spergillussp.
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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.
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Front Immunol.2018, 9:2655
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Phytother Res.2023, 37(10):4587-4606.
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Kangwon National University2022, 37(1):29-37
Univerzita Karlova2022, 173245.
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Front. Physiol.2022, 790345.
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Nat Prod Res. 2013;27(9):809-17.
Synthesis of (-)-albrassitriol and (-)-6-epi-albrassitriol from (+)-larixol.[Pubmed:
22794273 ]
A novel synthesis of natural drimanic compounds, (-)-albrassitriol (2) and (-)-6-epi-Albrassitriol (3), has been carried out starting from an easily available labdane diterpenoid, (+)-larixol (1).
METHODS AND RESULTS:
In a two-step procedure, (+)-larixol (1) was converted into 14,15-bisnorlab-7-ene-6,13-dione (9), which was then submitted to a Norrish type II photochemical degradation yielding drim-7,9(11)-diene-6-one (10), whose treatment with OsO4 led selectively to the formation of drim-7-ene-9α,11-diol-6-one (12). The same compound was obtained by selective epoxidation of the C(9)-C(11) double bond in drim-7,9(11)-diene-6-one (10) with monoperphtalic acid.
Treatment of the resulting mixture of α- and β-epoxides (13 and 14) with HClO4 yielded drim-7-ene-9α,11-diol-6-one (12). Reduction of the C6-carbonyl group in drim-7-ene-9α,11-diol-6-one (12) with LiAlH4 afforded (-)-albrassitriol (2) and (-)-6-epi-Albrassitriol (3), 12.4% and 13.6% overall yields, respectively.
