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ChemicalBook CAS DataBase List Ginsenoside Rg1
22427-39-0

Ginsenoside Rg1 synthesis

4synthesis methods
(1) Take the total saponin obtained from the extraction of Panax ginseng, ginseng, American ginseng or gynostemma, the total saponin is solubilized with water;

(2) the dissolved solution is filtered, the filtrate is passed through a non-po
-

Yield:-

Reaction Conditions:

with α-rhamnosidase in aq. acetate buffer at 32; for 22 h;Enzymatic reaction;

Steps:

1

Test Example 1: Analysis of saponinase [0049] Each of 50 mg of the standard Rg3 sample and 50 mg of the standard Re sample was added to 20 mM of sodium acetate buffer solution, and the saponinase of the present invention was added thereto. Then, each of the mixtures was stirred at a constant temperature of 32 °C for 22 hours. Each of the enzymatic reaction products was separated into layers by adding butanol thereto, and the butanol layer was concentrated and analyzed by HPLC. The HPLC analysis was performed under the following conditions. 1) Instrument: Shiseido nanospace SI-2 2) Column: Capcell Pak C18 UG80 4.6x150mm (5 μm) 3) Flow rate: 1.00mL/min 4) UV wavelength: 203nm 5) Column temperature: 40°C 6) Injection amount: 20μL 7) Mobile phase: Re analysis: 20% acetonitrile [0050] Rg3 analysis: concentration gradient with 40% acetonitrile and 60% acetonitrile for 40 minutes. [0051] From the test results, it could be seen that, when the standard Re was reacted with the enzyme of the present invention, Rg1 was produced, suggesting that α-rhamnosidase is present in the saponinase of the present invention. In addition, it could be seen that, when the standard Rg3 was reacted with the enzyme of the present invention, Rh2 was produced, suggesting that beta-glucosidase is present in the saponinase of the present invention (FIGS. 2 and 3).

References:

EP2570132,2013,A2 Location in patent:Paragraph 0049; 0050; 0051

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