5'-Methoxylariciresinol
5'-Methoxylariciresinol is a natural product from Stellera chamaejasme.
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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.
Int J Mol Sci.2018, 19(9):E2528
FEBS J.2022, 10.1111:febs.16676.
Korean Herb. Med. Inf.2020, 8(2):233-242.
bioRxiv - Biochemistry2023, 541790.
Internoational J of Toxicology2020, 10.1177.
Molecules. 2013, 18(7):7376-88
J Cell Mol Med.2018, 22(9):4236-4242
Biochem Pharmacol. 2020, 177:114014.
Aging (Albany NY).2023, 15(24):15557-15577.
J Mol Med (Berl).2018, 96(7):661-672
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Zhongguo Zhong Yao Za Zhi. 2011 Dec;36(24):3457-62.
Studies on chemical constitutes from callus cultures of Stellera chamaejasme.[Pubmed:
22368856]
METHODS AND RESULTS:
From callus cultures of Stellera chamaejasme, 17 compounds were isolated. Based on their physical and chemical data and spectroscopic analysis, they were identified as syringaresinol (1), medioresinol (2), pinoresinol (3), (1R, 2S, 5R, 6S)- 2-(4- hydroxyphenyl)-6-(3-methoxy-4-hydroxyphenyl)-3, 7-dioxabicyclo [3, 3, 0] octane (4), epipinoresinol (5), caruilignan D (6), 3-oxo-guai-4-ene-11, 12-diol (7), (-) -lariciresinol (8), tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxyphenyl) methyl]-3-furanmethanol (9), 5'-Methoxylariciresinol (10), vladinol D (11), cyclo (L-Pro-L-Val) (12), oxomatairesinol (13), (+) -guayarol (14); acutissimalignan B (15), isolariciresinol (16), and beta-sitosterol (17), respectively.
CONCLUSIONS:
Among these compounds, 12 was a cyclodipeptide, 7 was a sesquiterpene, and the others except 17 were lignans. All compounds were first isolated from callus cultures of S. chamaejasme.
Zhongguo Zhong Yao Za Zhi. 2012 May;37(9):1241-4.
Non-alkaloid chemical constituents from Coptis chinensis.[Pubmed:
22803368]
To separate and identify chemical constituents from Coptis chinensis.
METHODS AND RESULTS:
The compounds were separated and purified by various chromatographic techniques. Their structures were identified on the basis of their physicochemical properties using spectral techniques such as NMR and MS. Thirteen compounds were separated from ethanol extracts of C. chinensis, including seven lignans, three simple phenylpropanoids, two flavones and one phenolic acid, and identified as erythro-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether (1), threo-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether (2), (+)-pinoresinol (3), (+)-medioresinol (4), (+)-lariciresinol (5), (+)-5'-Methoxylariciresinol (6), (+)-isolariciresinol (7), chlorogenic acid (8), ferulic acid (9), Z-octadecyl caffeate (10), rhamnetin (11), wogonin (12), and vanillic acid (13).
CONCLUSIONS:
Compounds 1, 2, 4, 6, 10-13 were separated from the genus Coptis for the first time.
