Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List Ginsenoside Rg1

Ginsenoside Rg1 synthesis

4synthesis methods
-

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

Ginsenoside Rg1 Related Search: