Sophoracarpan ACAS# 1674359-82-0 |
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| Cas No. | 1674359-82-0 | SDF | Download SDF |
| PubChem ID | 131849416 | Appearance | Powder |
| Formula | C17H16O5 | M.Wt | 300.31 |
| Type of Compound | Phenols | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (6S,6aS,11aR)-6,9-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol | ||
| SMILES | COC1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)OC | ||
| Standard InChIKey | VDHFFCPQILOKFG-ULQDDVLXSA-N | ||
| Standard InChI | InChI=1S/C17H16O5/c1-19-10-4-6-11-14(8-10)21-16-12-5-3-9(18)7-13(12)22-17(20-2)15(11)16/h3-8,15-18H,1-2H3/t15-,16-,17-/m0/s1 | ||
| 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. | ||
The aerial parts of Sophora tomentosa L.
| Description | Sophoracarpan A is a natural product from Sophora tomentosa L. |
| Structure Identification | Chemical & Pharmaceutical Bulletin, 1990, 38(10):2756-2759.Chemical studies on Sophora tomentosa: the isolation of a new class of isoflavonoid.[Reference: WebLink]Two new pterocarpans, Sophoracarpan A and Sophoracarpan B, were isolated from Sophora tomentosa L. (Leguminosae) in addition to three known isoflavonoids, wighteone (erythrinin B), sophoraisoflavanone A and l-maackiain.
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Sophoracarpan A Dilution Calculator
Sophoracarpan A Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.3299 mL | 16.6495 mL | 33.2989 mL | 66.5978 mL | 83.2473 mL |
| 5 mM | 0.666 mL | 3.3299 mL | 6.6598 mL | 13.3196 mL | 16.6495 mL |
| 10 mM | 0.333 mL | 1.6649 mL | 3.3299 mL | 6.6598 mL | 8.3247 mL |
| 50 mM | 0.0666 mL | 0.333 mL | 0.666 mL | 1.332 mL | 1.6649 mL |
| 100 mM | 0.0333 mL | 0.1665 mL | 0.333 mL | 0.666 mL | 0.8325 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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Unified total syntheses of (-)-medicarpin, (-)-sophoracarpan A, and (+/-)-kushecarpin A with some structural revisions.[Pubmed:25476784]
Angew Chem Int Ed Engl. 2015 Feb 2;54(6):1864-7.
The total syntheses of medicarpin, Sophoracarpan A, and kushecarpin A from a common intermediate are achieved by using ortho- and para-quinone methide chemistry. Additionally, the relative stereochemistry of Sophoracarpan A and B have been reassigned.
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