Tetrahydro tanshinone ICAS# 126979-84-8 |
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
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Cas No. | 126979-84-8 | SDF | Download SDF |
PubChem ID | 124416 | Appearance | Red powder |
Formula | C18H16O3 | M.Wt | 280.31 |
Type of Compound | Diterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | 1,6-dimethyl-1,2,8,9-tetrahydronaphtho[1,2-g][1]benzofuran-10,11-dione | ||
SMILES | CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCC=C4C | ||
Standard InChIKey | AZIUYJPOBCMPON-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C18H16O3/c1-9-4-3-5-12-11(9)6-7-13-15(12)17(20)16(19)14-10(2)8-21-18(13)14/h4,6-7,10H,3,5,8H2,1-2H3 | ||
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. Tetrahydrotanshinone I is one compound of Fufang Danshen Prescription (FDP) , liposome equilibrium dialysis system could simply and effectively esti-mate the absorption of multiple components in FDP in vivo, and predicts the potential bioactivity of these components, and thus contributes to the investigation of bioactive compounds with curative effect in FDP. |
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Tetrahydro tanshinone I Dilution Calculator
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Tetrahydro tanshinone I Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 3.5675 mL | 17.8374 mL | 35.6748 mL | 71.3496 mL | 89.187 mL |
5 mM | 0.7135 mL | 3.5675 mL | 7.135 mL | 14.2699 mL | 17.8374 mL |
10 mM | 0.3567 mL | 1.7837 mL | 3.5675 mL | 7.135 mL | 8.9187 mL |
50 mM | 0.0713 mL | 0.3567 mL | 0.7135 mL | 1.427 mL | 1.7837 mL |
100 mM | 0.0357 mL | 0.1784 mL | 0.3567 mL | 0.7135 mL | 0.8919 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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Calcutta University
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University of Minnesota
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University of Maryland School of Medicine
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University of Illinois at Chicago
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The Ohio State University
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University of Zurich
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Harvard University
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Colorado State University
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Auburn University
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Yale University
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Worcester Polytechnic Institute
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Washington State University
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University of Leipzig
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TsingHua University
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The University of Michigan
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DRURY University
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Jilin University
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Fudan University
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Wuhan University
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Sun Yat-sen University
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Universite de Paris
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Deemed University
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Auckland University
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The University of Tokyo
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Interactions of Fufang Danshen Prescription with Liposome Biomembrane
《Chinese Journal of Natural Medicines》 2008-04
Six diterpenoid qui-nines (dihydrotanshinone I, Tetrahydro tanshinone I, cryptotanshinone, tanshinone I, methylene tanshiqunone and tanshinone IIA) and five saponins (notoginsenoside R1, ginsenoside Rg1, ginsenoside Rb1, ginsenoside Rd and notoginsenoside K). CONCLUSION: Liposome equilibrium dialysis system coupled with HPLC and LC/TOF/MS could simply and effectively esti-mate the absorption of multiple components in FDP in vivo, and predicts the potential bioactivity of these components, and thus contributes to the investigation of bioactive compounds with curative effect in FDP.