5-HydroxyxanthotoxinCAS# 7471-73-0 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 7471-73-0 | SDF | Download SDF |
| PubChem ID | 5385192 | Appearance | Powder |
| Formula | C12H8O5 | M.Wt | 232 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 4-hydroxy-9-methoxyfuro[3,2-g]chromen-7-one | ||
| SMILES | COC1=C2C(=C(C3=C1OC(=O)C=C3)O)C=CO2 | ||
| Standard InChIKey | XPFCGZWOHNGDSP-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C12H8O5/c1-15-12-10-7(4-5-16-10)9(14)6-2-3-8(13)17-11(6)12/h2-5,14H,1H3 | ||
| 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. | ||
5-Hydroxyxanthotoxin Dilution Calculator
5-Hydroxyxanthotoxin Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 4.3103 mL | 21.5517 mL | 43.1034 mL | 86.2069 mL | 107.7586 mL |
| 5 mM | 0.8621 mL | 4.3103 mL | 8.6207 mL | 17.2414 mL | 21.5517 mL |
| 10 mM | 0.431 mL | 2.1552 mL | 4.3103 mL | 8.6207 mL | 10.7759 mL |
| 50 mM | 0.0862 mL | 0.431 mL | 0.8621 mL | 1.7241 mL | 2.1552 mL |
| 100 mM | 0.0431 mL | 0.2155 mL | 0.431 mL | 0.8621 mL | 1.0776 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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The biosynthesis of isopimpinellin.[Pubmed:890566]
Can J Biochem. 1977 Jul;55(7):686-92.
Bergapten and xanthotoxin, labelling in the methyl group wich carbon-14 or tritiated at three skeletal carbons, were administered to leaves of Heracleum lanatum and to cell cultures of Ruta graveolens. In all experiments xanthotoxin was the more efficient precursor of isopimpinellin, although bergapten was always incorporated to a measurable extent. Double-labelling experiments showed that both precursors, especially bergapten, underwent considerable demethylation (and presumably remethylation) before conversion to isopimpinellin. 5-Hydroxyxanthotoxin and 8-hydroxybergapten were both O-methylated by cell-free extracts of Ruta cells to isopimpinellin, in reactions mediated by discrete O-methyltransferases. 8-Hydroxy[Me-14C]bergapten was converted with a high degree of incorporation to isopimpinellin by Ruta cells in vivo, and it is suggested that the preference for the pathway via xanthotoxin may be due to more rapid hydroxylation of this substrate.
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