Medicagol
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.
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Acta Edulis Fungi2020, 27(02):63-76.
Related and Featured Products
Journal of Organic Chemistry, 1965, 30(7):2353-2355.
Medicagol, a New Coumestan From Alfalfa.[Reference:
WebLink]
METHODS AND RESULTS:
A new coumestan, Medicagol(C16H8O6), has been identified in alfalfa. Characterization was accomplished by degradative and proton magnetic resonance (p.m.r.) studies.
CONCLUSIONS:
Synthesis confirmed the structure as 7-hydroxy-11,12-methyl-enedioxycoumestan, closely related to the antifungal agent, pisatin.
Journal of Asian Natural Products Research, 2002, 4(1):1-5.
A new Coumaronochromone from Sophora japonica.[Reference:
WebLink]
METHODS AND RESULTS:
A new coumaronochromone derivative, sophorophenolone (1), along with 13 known compounds, l-maackiain (2), Medicagol (3), 7-O-methylpseudobaptigenin (4), pseudobaptigenin (5), 7,3'-di-O-methylorobol (6), genistein (7), prunetin (8), daidzein (9), formononetin (10), Di-O-methyldaidzein (11), quercetin (12), kaempferol (13) and isorhamnetin (14) were isolated from pericarps of Sophorajaponica L.
CONCLUSIONS:
The structure of compound 1 was established by UV, IR, MS, and one-dimensional and two-dimensional NMR spectroscopy, including DEPT, NOESY, 1H-1H COSY, HMQC, and HMBC experiments.
