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7-Prenyljacareubin

CAS# 94513-60-7

7-Prenyljacareubin

Catalog No. BCN7353----Order now to get a substantial discount!

Product Name & Size Price Stock
7-Prenyljacareubin:5mg Please Inquire In Stock
7-Prenyljacareubin:10mg Please Inquire In Stock
7-Prenyljacareubin:20mg Please Inquire In Stock
7-Prenyljacareubin:50mg Please Inquire In Stock

Quality Control of 7-Prenyljacareubin

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Chemical structure

7-Prenyljacareubin

3D structure

Chemical Properties of 7-Prenyljacareubin

Cas No. 94513-60-7 SDF Download SDF
PubChem ID 124355832 Appearance Powder
Formula C23H22O6 M.Wt 394.42
Type of Compound Xanthones Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 5,9,10-trihydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
SMILES CC(=CCC1=C(C(=C2C(=C1)C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)O)C
Standard InChIKey FKBCRWZDPJSICF-UHFFFAOYSA-N
Standard InChI InChI=1S/C23H22O6/c1-11(2)5-6-12-9-14-20(26)17-16(28-22(14)21(27)18(12)24)10-15-13(19(17)25)7-8-23(3,4)29-15/h5,7-10,24-25,27H,6H2,1-4H3
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 7-Prenyljacareubin

The stem barks of Garcinia paucinervis.

Biological Activity of 7-Prenyljacareubin

Description1. 7-Prenyljacareubin shows moderate cytotoxic activity against HL-60, SMMC-7721, A549, MCF-7, and SW480 cell lines.

7-Prenyljacareubin Dilution Calculator

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7-Prenyljacareubin Molarity Calculator

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Preparing Stock Solutions of 7-Prenyljacareubin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5354 mL 12.6768 mL 25.3537 mL 50.7074 mL 63.3842 mL
5 mM 0.5071 mL 2.5354 mL 5.0707 mL 10.1415 mL 12.6768 mL
10 mM 0.2535 mL 1.2677 mL 2.5354 mL 5.0707 mL 6.3384 mL
50 mM 0.0507 mL 0.2535 mL 0.5071 mL 1.0141 mL 1.2677 mL
100 mM 0.0254 mL 0.1268 mL 0.2535 mL 0.5071 mL 0.6338 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 7-Prenyljacareubin

Chemical constituents from stem barks of Garcinia paucinervis.

Chinese Traditional & Herbal Drugs, 2012, 43(3):436-439.

To study the chemical constituents from the stem barks of Garcinia paucinervis and their antitumor activities. Methods Chemical constituents were isolated and purified from petroleum ether extract of G. paucinervis by chromatography on silica gel, RP-18, Sephadex LH-20 column, and preparative TLC. Their structures were identified on the basis of spectroscopic analysis and chemical evidence. The antitumor activity was screened by MTT assay. Results Ten compounds were isolated and identified as cambogin (1), pyromeconic acid (2), β-sitosterol (3), daucosterol (4), 7-Prenyljacareubin (5), parvifolixanthone A (6), formoxanthone A (7), termicalcicolanone A (8), 1, 3, 5, 6-tetrahydroxy-4-prenylxanthone (9), and isogarcinol (10). Compounds 5 and 7 showed moderate cytotoxic activity against HL-60, SMMC-7721, A549, MCF-7, and SW480 cell lines. Conclusion Compounds 2-5 and 7-10 are isolated from this plant for the first time and the 13C-NMR spectroscopic data of compound 5 are firstly reported.

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