CuspidiolCAS# 51593-96-5 |
Quality Control & MSDS
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Number of papers citing our products
| Cas No. | 51593-96-5 | SDF | Download SDF |
| PubChem ID | 6509776 | Appearance | Powder |
| Formula | C14H20O3 | M.Wt | 236.3 |
| Type of Compound | Phenylpropanoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (E)-4-[4-(3-hydroxypropyl)phenoxy]-2-methylbut-2-en-1-ol | ||
| SMILES | CC(=CCOC1=CC=C(C=C1)CCCO)CO | ||
| Standard InChIKey | GAXDMZRXKOERED-XYOKQWHBSA-N | ||
| Standard InChI | InChI=1S/C14H20O3/c1-12(11-16)8-10-17-14-6-4-13(5-7-14)3-2-9-15/h4-8,15-16H,2-3,9-11H2,1H3/b12-8+ | ||
| 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 | 1. Cuspidiol shows cytotoxicity against Jurkat T cell clone E6.1 at 7.3 ug/mL. |
Cuspidiol Dilution Calculator
Cuspidiol Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 4.2319 mL | 21.1595 mL | 42.3191 mL | 84.6382 mL | 105.7977 mL |
| 5 mM | 0.8464 mL | 4.2319 mL | 8.4638 mL | 16.9276 mL | 21.1595 mL |
| 10 mM | 0.4232 mL | 2.116 mL | 4.2319 mL | 8.4638 mL | 10.5798 mL |
| 50 mM | 0.0846 mL | 0.4232 mL | 0.8464 mL | 1.6928 mL | 2.116 mL |
| 100 mM | 0.0423 mL | 0.2116 mL | 0.4232 mL | 0.8464 mL | 1.058 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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Cytotoxic Constituents from the Leaves of Zanthoxylum schinifoliu.
Bull. Korean Chem. Soc., 2010, 31(4):1081-4.
The results showed that the methylene chloride fraction exhibited the strongest MTT cytotoxicity. Chromatographic separation of the methylene chloride and butanol fractions had yielded a quinolin (1), three phenylpropanoids (2, 3, 12), four coumarins (4 ~ 7), three triterpenoids (8 ~ 10), an alkaloid (11), an alcohol glucoside (13) and three monoterpene glucosides (14, 15, 16). One of these compounds were identified as new threo-6-amino-5-hydroxy-5-methyl- 1,3-oxazinan-4-one (11) together with fifteen known, 3-heptyl- 2-methylisoquinolin-1(2H)-one (1), integrifoliodiol (2), Cuspidiol (3), bergapten (4), aurapten (5), 8-hydroxy-7-methoxy- chromen-2-one (6), 6,7-dimethoxy-2H-naphthalen-1-one (7), lupeol (8), lupeone (9), β-sitosterol (10), syringin (12), 2-propyl alchol β-D-glucopyranoside (13), vomifoliol-9-O-β-D-glucopyranoside (14), betulalbuside A (15) and cnidioside C (16) on the basis of spectroscopic and chemical evidences. All of the compounds were isolated for the first time from this plant except 5 and 7. In the MTT cytotoxicity assay against Jurkat T cell clone E6.1, IC50 values of Cuspidiol (3) and auraptene (5) were obtained at 7.3 μg/mL and 16.5 μg/mL, respectively
