Parvifolixanthone ACAS# 906794-56-7 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 906794-56-7 | SDF | Download SDF |
| PubChem ID | 16085273 | Appearance | Powder |
| Formula | C28H32O6 | M.Wt | 464.55 |
| Type of Compound | Xanthones | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 1,3,5,6-tetrahydroxy-2,4,7-tris(3-methylbut-2-enyl)xanthen-9-one | ||
| SMILES | CC(=CCC1=C(C(=C2C(=C1)C(=O)C3=C(O2)C(=C(C(=C3O)CC=C(C)C)O)CC=C(C)C)O)O)C | ||
| Standard InChIKey | UVAAZIOBAWMBHC-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C28H32O6/c1-14(2)7-10-17-13-20-25(32)21-24(31)18(11-8-15(3)4)23(30)19(12-9-16(5)6)27(21)34-28(20)26(33)22(17)29/h7-9,13,29-31,33H,10-12H2,1-6H3 | ||
| 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. |
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| 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. |
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| 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. | ||
| Description | Parvifolixanthone A is a natural product from Garcinia parvifolia. |
| In vitro | Chemical constituents from stem barks of Garcinia paucinervis.[Reference: WebLink]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. |
| Structure Identification | Tetrahedron, 2006, 62(36):8578-8585.Phloroglucinols, depsidones and xanthones from the twigs of Garcinia parvifolia.[Reference: WebLink]
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Parvifolixanthone A Dilution Calculator
Parvifolixanthone A Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.1526 mL | 10.7631 mL | 21.5262 mL | 43.0524 mL | 53.8155 mL |
| 5 mM | 0.4305 mL | 2.1526 mL | 4.3052 mL | 8.6105 mL | 10.7631 mL |
| 10 mM | 0.2153 mL | 1.0763 mL | 2.1526 mL | 4.3052 mL | 5.3816 mL |
| 50 mM | 0.0431 mL | 0.2153 mL | 0.4305 mL | 0.861 mL | 1.0763 mL |
| 100 mM | 0.0215 mL | 0.1076 mL | 0.2153 mL | 0.4305 mL | 0.5382 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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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 the13C-NMR spectroscopic data of compound 5 are firstly reported.
