Floribundone 1

CAS# 118555-84-3

Floribundone 1

2D Structure

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3D structure

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Floribundone 1

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Chemical Properties of Floribundone 1

Cas No. 118555-84-3 SDF Download SDF
PubChem ID 11757663 Appearance Orange powder
Formula C32H22O10 M.Wt 566.52
Type of Compound Anthraquinones Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-(4,5-dihydroxy-2-methoxy-7-methyl-9,10-dioxoanthracen-1-yl)-1,8-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione
SMILES CC1=CC(=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C4=C5C(=C(C=C4OC)O)C(=O)C6=C(C=C(C=C6C5=O)C)O)OC)O
Standard InChIKey BJHQTGSKKZLDSE-UHFFFAOYSA-N
Standard InChI InChI=1S/C32H22O10/c1-11-5-13-21(16(33)7-11)30(38)23-15(28(13)36)9-19(41-3)26(32(23)40)25-20(42-4)10-18(35)24-27(25)29(37)14-6-12(2)8-17(34)22(14)31(24)39/h5-10,33-35,40H,1-4H3
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Floribundone 1

The herbs of Senna septemtrionalis

Biological Activity of Floribundone 1

DescriptionStandard reference

Protocol of Floribundone 1

Structure Identification
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.

Floribundone 1 Dilution Calculator

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Preparing Stock Solutions of Floribundone 1

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.7652 mL 8.8258 mL 17.6516 mL 35.3033 mL 44.1291 mL
5 mM 0.353 mL 1.7652 mL 3.5303 mL 7.0607 mL 8.8258 mL
10 mM 0.1765 mL 0.8826 mL 1.7652 mL 3.5303 mL 4.4129 mL
50 mM 0.0353 mL 0.1765 mL 0.353 mL 0.7061 mL 0.8826 mL
100 mM 0.0177 mL 0.0883 mL 0.1765 mL 0.353 mL 0.4413 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Floribundone 1

A new bianthracene C-arabinopyranoside from Senna septemtrionalis.[Pubmed:20521540]

Nat Prod Commun. 2010 May;5(5):747-50.

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.

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