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Chemical Structure| 199796-12-8 Chemical Structure| 199796-12-8

Structure of 199796-12-8

Chemical Structure| 199796-12-8

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Liquiritin apioside is purified from the roots of glycyrrhiza uralensis fisch and it has antioxidant effects by inducing glutathione (GSH) biosynthesis via the inhibition of cytokines.

Synonyms: Liguiritigenin-7-O-D-apiosyl-4'-O-D-glucoside

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Product Details of Liguiritigenin-7-O-D-apiosyl-4'-O-D-glucoside

CAS No. :199796-12-8
Formula : C26H30O13
M.W : 550.51
SMILES Code : O=C1C[C@@H](C2=CC=C(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)C=C2)OC4=C1C=CC(O[C@@H]5OC[C@@](CO)(O)[C@H]5O)=C4
Synonyms :
Liguiritigenin-7-O-D-apiosyl-4'-O-D-glucoside

Safety of Liguiritigenin-7-O-D-apiosyl-4'-O-D-glucoside

Isoform Comparison

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.82mL

0.36mL

0.18mL

9.08mL

1.82mL

0.91mL

18.16mL

3.63mL

1.82mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2
 

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