Pseudoginsenoside RT5CAS# 98474-78-3 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 98474-78-3 | SDF | Download SDF |
PubChem ID | 21633075 | Appearance | White powder |
Formula | C36H62O10 | M.Wt | 654.88 |
Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in chloroform, ethanol, methanol and water | ||
Chemical Name | (2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-dihydroxy-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | ||
SMILES | CC1(C(CCC2(C1C(CC3(C2CC(C4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)O)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C | ||
Standard InChIKey | PSOUXXNNRFNUAY-JLXGCTMESA-N | ||
Standard InChI | InChI=1S/C36H62O10/c1-31(2)23(39)10-12-33(5)22-15-19(38)25-18(36(8)14-11-24(46-36)32(3,4)43)9-13-34(25,6)35(22,7)16-20(29(31)33)44-30-28(42)27(41)26(40)21(17-37)45-30/h18-30,37-43H,9-17H2,1-8H3/t18-,19+,20-,21+,22+,23-,24+,25-,26+,27-,28+,29-,30+,33+,34+,35+,36-/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. |
Description | Pseudoginsenoside RT5 is a nartural product from Panax ginseng C. A. Mey. |
In vitro | Research on dynamic accumulation of nine ginsenosides and two pseudo-ginsenosides of Panax quinquefolium root of different growth years and harvest months in Canada.[Pubmed: 25895377]Zhong Yao Cai. 2014 Oct;37(10):1743-8.RP-HPLC-ELSD was adopted. The analysis was performed on a Dimaonsil C18 (250 mm x 4.6 mm, 5 μm) column, the mobile phase was acetonitrile (A)-deionized water (B) in gradient elution mode. |
Structure Identification | Zhongguo Zhong Yao Za Zhi. 2003 Sep;28(9):830-3.[Studies on saponin constituents in roots of Panax quinquefolium].[Pubmed: 15015374]To examine the saponins constituents in roots of Panax quinquefolium cultivated in China.
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Pseudoginsenoside RT5 Dilution Calculator
Pseudoginsenoside RT5 Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 1.527 mL | 7.635 mL | 15.27 mL | 30.5399 mL | 38.1749 mL |
5 mM | 0.3054 mL | 1.527 mL | 3.054 mL | 6.108 mL | 7.635 mL |
10 mM | 0.1527 mL | 0.7635 mL | 1.527 mL | 3.054 mL | 3.8175 mL |
50 mM | 0.0305 mL | 0.1527 mL | 0.3054 mL | 0.6108 mL | 0.7635 mL |
100 mM | 0.0153 mL | 0.0763 mL | 0.1527 mL | 0.3054 mL | 0.3817 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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[Studies on saponin constituents in roots of Panax quinquefolium].[Pubmed:15015374]
Zhongguo Zhong Yao Za Zhi. 2003 Sep;28(9):830-3.
OBJECTIVE: To examine the saponins constituents in roots of Panax quinquefolium cultivated in China. METHOD: The methanol extract from roots of P. quinquefolium cultivated in Jiling province of China was extracted by chloroform and n-butanol successively. Ten pure saponins were isolated from the n-butanol extract by silica gel and RP-8 reversed-phase column chromatography. Their structures were identified by means of spectral methods and compared with known compounds. RESULT: Ten saponins were isolated from P. quinquefolium. They were identified as ginsenoside Rg1(2), Re(5), Rd(7), Rc(8), Rb1(9), Rb2(10), 24(R)-ginsenoside Rg3(3), 24(R)-Pseudoginsenoside RT5(1), F11(4) and notoginsenoside K(6), respectively. CONCLUSION: This work has elucidated the saponins constituents of P. quinquefolium cultivated in Jilin province of China and has shown that compound 1 was isolated from this plant for the first time.