Racemoflavone

CAS# 106055-12-3

Racemoflavone

Catalog No. BCX0295----Order now to get a substantial discount!

Product Name & Size Price Stock
Racemoflavone: 5mg $989 In Stock
Racemoflavone: 10mg Please Inquire In Stock
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Quality Control of Racemoflavone

Number of papers citing our products

Chemical structure

Racemoflavone

Chemical Properties of Racemoflavone

Cas No. 106055-12-3 SDF Download SDF
PubChem ID N/A Appearance Yellow powder
Formula C21H18O6 M.Wt 366.39
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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.

Racemoflavone Dilution Calculator

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Racemoflavone Molarity Calculator

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Preparing Stock Solutions of Racemoflavone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.7293 mL 13.6467 mL 27.2933 mL 54.5866 mL 68.2333 mL
5 mM 0.5459 mL 2.7293 mL 5.4587 mL 10.9173 mL 13.6467 mL
10 mM 0.2729 mL 1.3647 mL 2.7293 mL 5.4587 mL 6.8233 mL
50 mM 0.0546 mL 0.2729 mL 0.5459 mL 1.0917 mL 1.3647 mL
100 mM 0.0273 mL 0.1365 mL 0.2729 mL 0.5459 mL 0.6823 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 Racemoflavone

A new flavonoid from the leaves of Atalantia monophylla (L.) DC.[Pubmed:29600742]

Nat Prod Res. 2019 Apr;33(8):1115-1121.

A new flavonoid, atalantraflavone (1) as well as eight known compounds including atalantoflavone (2), Racemoflavone (3), 5,4'-dihydroxy-(3'',4''-dihydro-3'',4''-dihydroxy)-2'',2''-dimethylpyrano-(5'',6'':7,8)-flavone (4), lupalbigenin (5), anabellamide (6), citrusinine I (7), p-hydroxybenzaldehyde (8), and frideline (9), were isolated from the leaves of Atalantia monophylla (L.) DC. Focusing on Alzheimer's disease, acetylcholine esterase (AChE) inhibition and antioxidant activity were evaluated using the modified Ellman's method and the ABTS scavenging assay, respectively. It was found that isoflavonoid 5, lupalbigenin, showed 79% inhibition to AChE and was 1.4-fold stronger than the tacrine standard. In addition, acridone 7, citrusinine I, displayed 90.68% antioxidant activity.

[Study on Chemical Constituents of Peanut Hull].[Pubmed:26415405]

Zhong Yao Cai. 2015 Feb;38(2):302-4.

OBJECTIVE: To investigate the chemical constituents of peanut hull. METHODS: Several chromatography methods such as silica gel and Sephadex LH-20 combined with recrystallization were applied to isolate the compounds. Based on spectrum technologies (MS,1H-NMR and 13C-NMR) and physico-chemical methods, structures of isolated compounds were identified. RESULTS: Twelve compounds were isolated and elucidated as luteolin (1), diosmetin (2), 5,7,3',4'-tetrahydroxy-8-prenyflavone (3),5,7,3'-trihydroxy-4'- methoxy-8-prenylflavone(4), eriodicrtyol (5), Racemoflavone (6), hydnocarpin (7), 5,7-dihydroxy chromone (8), 5-hydroxy-chromone- 7-O-beta-D-glucoside (9), ferulic acid (10), beta-sitosterol (11) and daucosterol(12). CONCLUSION: Except compounds 1, 5 and 8, all compounds are obtained from peanut hull for the first time.

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