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Chemical Structure| 59870-68-7 Chemical Structure| 59870-68-7

Structure of Glabridin
CAS No.: 59870-68-7

Chemical Structure| 59870-68-7

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Glabridin has many biological functions such as regulating the synthesis and activity of iNOS under high-glucose levels, significantly inhibiting free radicals generated during metabolism in the body, and protecting against oxidation-sensitive biomacromolecules (LDL, LDL, DNA) and cell walls. It is a natural product isolated and purified from the roots of Glycyrrhiza glabra L. with whitening and anti-aging activity.

Synonyms: Q-100692; KB-289522; LS-176045

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Product Details of Glabridin

CAS No. :59870-68-7
Formula : C20H20O4
M.W : 324.37
SMILES Code : OC1=CC=C([C@H]2CC3=CC=C4C(C=CC(C)(C)O4)=C3OC2)C(O)=C1
Synonyms :
Q-100692; KB-289522; LS-176045
MDL No. :MFCD03427694
InChI Key :LBQIJVLKGVZRIW-ZDUSSCGKSA-N
Pubchem ID :124052

Safety of Glabridin

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.08mL

0.62mL

0.31mL

15.41mL

3.08mL

1.54mL

30.83mL

6.17mL

3.08mL

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

References

[1]Yehuda I, Madar Z, et al. Glabridin, an isoflavan from licorice root, downregulates iNOS expression and activity under high-glucose stress and inflammation. Mol Nutr Food Res. 2015 Jun;59(6):1041-52.

[2]Hsieh MJ, Lin CW, et al. Glabridin inhibits migration and invasion by transcriptional inhibition of matrix metalloproteinase 9 through modulation of NF-κB and AP-1 activity in human liver cancer cells. Br J Pharmacol. 2014 Jun;171(12):3037-50.

[3]Hespeler D, Kaltenbach J, Pyo SM. Glabridin smartPearls - Silica selection, production, amorphous stability and enhanced solubility. Int J Pharm. 2019 Apr 20;561:228-235. doi: 10.1016/j.ijpharm.2019.02.028. Epub 2019 Mar 2. PMID: 30836152.

[4]Li LJ, Li GW, Xie Y. Zhongguo Zhong Yao Za Zhi. 2019;44(17):3786-3791.

[5]Mu J, Zhu D, Shen Z, Ning S, Liu Y, Chen J, Li Y, Li Z. The repressive effect of miR-148a on Wnt/β-catenin signaling involved in Glabridin-induced anti-angiogenesis in human breast cancer cells. BMC Cancer. 2017 May 2;17(1):307. doi: 10.1186/s12885-017-3298-1. PMID: 28464803; PMCID: PMC5414299.

[6]Hsieh MJ, Lin CW, Yang SF, Chen MK, Chiou HL. Glabridin inhibits migration and invasion by transcriptional inhibition of matrix metalloproteinase 9 through modulation of NF-κB and AP-1 activity in human liver cancer cells. Br J Pharmacol. 2014 Jun;171(12):3037-50. doi: 10.1111/bph.12626. Erratum in: Br J Pharmacol. 2017 May;174(9):909-910. PMID: 24641665; PMCID: PMC4055204.

[7]Huang HL, Hsieh MJ, Chien MH, Chen HY, Yang SF, Hsiao PC. Glabridin mediate caspases activation and induces apoptosis through JNK1/2 and p38 MAPK pathway in human promyelocytic leukemia cells. PLoS One. 2014 Jun 5;9(6):e98943. doi: 10.1371/journal.pone.0098943. PMID: 24901249; PMCID: PMC4047044.

[8]Kwon HS, Oh SM, Kim JK. Glabridin, a functional compound of liquorice, attenuates colonic inflammation in mice with dextran sulphate sodium-induced colitis. Clin Exp Immunol. 2008 Jan;151(1):165-73. doi: 10.1111/j.1365-2249.2007.03539.x. Epub 2007 Nov 14. PMID: 18005263; PMCID: PMC2276918.

 

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