Floribundone 1
Standard reference
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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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Related and Featured Products
Nat Prod Commun. 2010 May;5(5):747-50.
A new bianthracene C-arabinopyranoside from Senna septemtrionalis.[Pubmed:
20521540 ]
METHODS AND RESULTS:
Chrysophanol, physcion, emodin, Floribundone 1, 5,7'-physcion-fallacinol, and the novel 5,7'-physcion-physcion-10'-C-alpha-arabinopyranoside were isolated from the stem bark of Senna septemtrionalis. The structures of these secondary metabolites were determined on the basis of spectroscopic analysis, especially from NMR spectra in conjunction with COSY, HMQC, HMBC and TOCSY.
Phytochemistry.1994 Jan;35(2):465–468.
Anthraquinones from Senna multiglandulosa.[Reference:
WebLink]
METHODS AND RESULTS:
Emodin and four bianthraquinones: Floribundone 1, torosanin-9′,10′-quinone, anhydrophlegmacin and a new bianthraquinone containing a 1,4-quinone moiety, 9-(physcion-7′-yl)-5,10-dihydroxy-2-methoxy-7-methyl-1,4-anthraquinone, are reported from Senna multiglandulosa. The compounds are identified on the basis of their colour reactions and spectroscopic data. A bianthraquinone structure containing a 1,4-quinone moiety is reported for the first time.
