Glycyrrhizic acid
Based on 59 publication(s) in Google Scholar
Glycyrrhizic acid is a triterpenoid saponinl, acting as a direct HMGB1 antagonist, with anti-tumor, anti-diabetic activities.
For research use only. We do not sell to patients.
- Purity: 99.84%
- CAS No.: 1405-86-3
- Formula: C42H62O16
- Molecular Weight:822.93
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Publications Citing Use of MedChemExpress (MCE) Glycyrrhizic acid
More- Nat Nanotechnol. 2025 May 19. [Abstract]
- Adv Sci (Weinh). 2024 Aug 5:e2404408. [Abstract]
- Chem Eng J. 2025 May 1.
- J Exp Clin Cancer Res. 2024 Apr 4;43(1):105. [Abstract]
- Mater Today Bio. 2025 Dec 8:36:102657. [Abstract]
- Mater Today Bio. 2025 Apr 17:32:101778. [Abstract]
- Adv Healthc Mater. 2024 Jan;13(2):e2301808. [Abstract]
- Cell Commun Signal. 2023 May 1;21(1):86. [Abstract]
- Phytomedicine. 2025 Sep:145:157081. [Abstract]
- Phytomedicine. 2025 Jul:142:156713. [Abstract]
- Phytomedicine. 2024 Dec:135:156059. [Abstract]
- Food Res Int. 2025 Dec;222(Pt 1):117620. [Abstract]
- Redox Rep. 2025 Dec;30(1):2585221. [Abstract]
- Cell Death Discov. 2024 Jan 17;10(1):34. [Abstract]
- EMBO Rep. 2025 Nov 17. [Abstract]
- Cell Prolif. 2024 Nov 20:e13774. [Abstract]
- Cell Prolif. 2020 Jun;53(6):e12829. [Abstract]
- Drug Des Devel Ther. 2025 Apr 2:19:2503-2517. [Abstract]
- CNS Neurosci Ther. 2025 May;31(5):e70406. [Abstract]
- Pharmaceuticals (Basel). 2022 Jan 31;15(2):179. [Abstract]
- Pharm Biol. 2020 Dec;58(1):898-904. [Abstract]
- Eur J Pharmacol. 2025 Oct 5:1004:177971. [Abstract]
- Int Immunopharmacol. 2025 Mar 26:150:114294. [Abstract]
- Int Immunopharmacol. 2025 Feb 3:149:114192. [Abstract]
- Neuropharmacology. 2025 Nov 15:279:110617. [Abstract]
- Hepatol Commun. 2023 Dec 22;8(1):e0350. [Abstract]
- Rheumatology (Oxford). 2025 Aug 13:keaf437. [Abstract]
- Mol Neurobiol. 2025 May;62(5):6070-6087. [Abstract]
- Front Cell Dev Biol. 2020 Aug 11;8:713. [Abstract]
- J Cell Mol Med. 2025 Nov;29(21):e70944. [Abstract]
- Mediators Inflamm. 2025 Jul 11:2025:2395557. [Abstract]
- J Inflamm Res. 2025 May 25:18:6735-6748. [Abstract]
- J Funct Foods. 2021, 104584.
- Sci Rep. 2025 Nov 12;15(1):39708. [Abstract]
- Fish Shellfish Immunol. 2024 Jan:144:109261. [Abstract]
- ACS Chem Neurosci. 2020 Mar 18;11(6):979-993. [Abstract]
- Aging (Albany NY). 2019 Jul 7;11(13):4323-4337. [Abstract]
- Cell Signal. 2024 Mar:115:111036. [Abstract]
- Eur J Med Res. 2025 Oct 9;30(1):943. [Abstract]
- Cardiovasc Drugs Ther. 2026 Jan 24. [Abstract]
- 3 Biotech. 2020 Aug;10(8):369. [Abstract]
- Vet Microbiol. 2026 May:316:110992. [Abstract]
- Toxicol In Vitro. 2025 Oct:108:106104. [Abstract]
- BMC Immunol. 2021 May 27;22(1):34. [Abstract]
- Adv Biol (Weinh). 2025 Jun 4:e00761. [Abstract]
- Behav Brain Res. 2025 May 24:115662. [Abstract]
- Biochem Biophys Res Commun. 2021 Feb 12:540:22-28. [Abstract]
- World Neurosurg. 2022 Feb:158:e856-e864. [Abstract]
- Planta Med. 2021 Jun;87(7):538-549. [Abstract]
- Rev Bras Farmacogn. 2023 Jun 28.
- SSRN. 2025 Nov 20.
- Res Sq. 2025 Oct 28.
- SSRN. 2025 Jul 8.
- bioRxiv. 2025 Feb 19.
- SSRN. 2025 Jan 15.
- Research Square Preprint. 2023 Apr 27.
- Research Square Print. August 24th, 2022.
- Research Square Preprint. 2022 May.
- Evid Based Complement Alternat Med. 2020 May 31;2020:8653783. [Abstract]
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WB
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In Vivo Efficacy Study
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RT-PCR
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Histological Imaging/Staining
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WB
Biological Activity
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Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
80.3 μM
Compound: GL
|
Cytotoxicity against human A549 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
|
[PMID: 37542990] |
| ECV-304 | IC50 |
>119 μM
Compound: Glycyrrhizinic acid
|
Cytotoxicity against human ECV304 cells after 72 hrs by MTT assay
Cytotoxicity against human ECV304 cells after 72 hrs by MTT assay
|
[PMID: 24084294] |
| ECV-304 | IC50 |
>238 μM
Compound: Glycyrrhizinic acid
|
Membrane toxicity against human ECV304 cells after 2 hrs by LDH release assay
Membrane toxicity against human ECV304 cells after 2 hrs by LDH release assay
|
[PMID: 24084294] |
| H9c2 | IC50 |
102.4 μM
Compound: GL
|
Cytotoxicity against rat H9c2 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against rat H9c2 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
|
[PMID: 37542990] |
| HEK293 | IC50 |
1 nM
Compound: glycyrrhizic acid
|
Inhibition of human microsomal 11beta-HSD2 expressed in HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
Inhibition of human microsomal 11beta-HSD2 expressed in HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
|
[PMID: 19564108] |
| HEK293 | IC50 |
10 nM
Compound: glycyrrhizic acid
|
Inhibition of human microsomal 11beta-HSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
Inhibition of human microsomal 11beta-HSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
|
[PMID: 19564108] |
| HEK293 | IC50 |
8 nM
Compound: glycyrrhizic acid
|
Inhibition of mouse microsomal 11beta-HSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
Inhibition of mouse microsomal 11beta-HSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
|
[PMID: 19564108] |
| HEK293 | IC50 |
0.015 μM
Compound: glycyrrhizic acid
|
Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation proximity assay
Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation proximity assay
|
[PMID: 19574056] |
| HEK293 | IC50 |
0.7 nM
Compound: glycyrrhizinic acid
|
Inhibition of human 11beta-HSD2 expressed in human HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
Inhibition of human 11beta-HSD2 expressed in human HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
|
[PMID: 22148241] |
| HEK293 | IC50 |
18.6 nM
Compound: glycyrrhizinic acid
|
Inhibition of human 11beta-HSD1 expressed in human HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
Inhibition of human 11beta-HSD1 expressed in human HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
|
[PMID: 22148241] |
| HEK293 | IC50 |
29.5 nM
Compound: glycyrrhizinic acid
|
Inhibition of mouse 11beta-HSD1 expressed in human HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
Inhibition of mouse 11beta-HSD1 expressed in human HEK293 cells assessed as conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay
|
[PMID: 22148241] |
| HEK293 | IC50 |
0.4 nM
Compound: glycyrrhizinic acid
|
Inhibition of human 11beta-HSD2 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation proximity assay
Inhibition of human 11beta-HSD2 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation proximity assay
|
[PMID: 22360639] |
| HEK293 | IC50 |
3 nM
Compound: glycyrrhizinic acid
|
Inhibition of mouse 11beta-HSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation proximity assay
Inhibition of mouse 11beta-HSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation proximity assay
|
[PMID: 22360639] |
| HEK293 | IC50 |
6 nM
Compound: glycyrrhizinic acid
|
Inhibition of human 11beta-HSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation proximity assay
Inhibition of human 11beta-HSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation proximity assay
|
[PMID: 22360639] |
| HEK293 | EC50 |
1 nM
Compound: Glycyrrhizic acid
|
Inhibition of human 11beta-HSD2 expressed in HEK293 cells assessed as [3H]cortisol production after 60 mins by SPA
Inhibition of human 11beta-HSD2 expressed in HEK293 cells assessed as [3H]cortisol production after 60 mins by SPA
|
[PMID: 22440625] |
| HEK293 | EC50 |
10 nM
Compound: Glycyrrhizic acid
|
Inhibition of human 11beta-HSD1 expressed in HEK293 cells assessed as [3H]cortisol production after 60 mins by SPA
Inhibition of human 11beta-HSD1 expressed in HEK293 cells assessed as [3H]cortisol production after 60 mins by SPA
|
[PMID: 22440625] |
| HEK293 | EC50 |
8 nM
Compound: Glycyrrhizic acid
|
Inhibition of mouse 11beta-HSD1 expressed in HEK293 cells assessed as [3H]cortisol production after 60 mins by SPA
Inhibition of mouse 11beta-HSD1 expressed in HEK293 cells assessed as [3H]cortisol production after 60 mins by SPA
|
[PMID: 22440625] |
| Hepatocyte | IC50 |
>200 μM
Compound: glycyrrizhin
|
Hepatoprotective activity against D-galactosamine/TNFalpha-induced cell death in primary cultured mouse hepatocytes treated for 30 mins before TNFalpha challenge measured after 18 hrs by MTT assay
Hepatoprotective activity against D-galactosamine/TNFalpha-induced cell death in primary cultured mouse hepatocytes treated for 30 mins before TNFalpha challenge measured after 18 hrs by MTT assay
|
[PMID: 11277757] |
| Hepatocyte | IC50 |
82.4 μM
Compound: glycyrrhizin
|
Hepatoprotective activity in mouse hepatocytes assessed inhibition of D-galactosamine/TNFalpha-induced cell death dosed administered before 30 mins of TNFalpha challenge measured after 18 hrs
Hepatoprotective activity in mouse hepatocytes assessed inhibition of D-galactosamine/TNFalpha-induced cell death dosed administered before 30 mins of TNFalpha challenge measured after 18 hrs
|
[PMID: 11325227] |
| Hepatocyte | IC50 |
>200 μM
Compound: 202
|
Hepatoprotective activity against D-GaIN/TNFalpha-induced cell death in mouse hepatocyte at 100 uM relative to control
Hepatoprotective activity against D-GaIN/TNFalpha-induced cell death in mouse hepatocyte at 100 uM relative to control
|
[PMID: 29353722] |
| Hepatocyte | IC50 |
9.3 μM
Compound: 202
|
Hepatotoxicity in D-GaIN induced in Wistar rat model hepatocyte assessed as reduction in PLA2 level
Hepatotoxicity in D-GaIN induced in Wistar rat model hepatocyte assessed as reduction in PLA2 level
|
[PMID: 29353722] |
| HK-2 | IC50 |
160.3 μM
Compound: GL
|
Cytotoxicity against human HK-2 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against human HK-2 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
|
[PMID: 37542990] |
| Huh-7 | IC50 |
65.7 μM
Compound: GL
|
Cytotoxicity against human Huh-7 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against human Huh-7 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
|
[PMID: 37542990] |
| MDCK | IC50 |
39.6 μM
Compound: 112
|
Antiviral activity against Influenza A virus A/WSN/33(H1N1) infected in dog MDCK cells preincubated with virus for 15 mins followed by cells addition measured at 36 hrs post infection
Antiviral activity against Influenza A virus A/WSN/33(H1N1) infected in dog MDCK cells preincubated with virus for 15 mins followed by cells addition measured at 36 hrs post infection
|
[PMID: 26841168] |
| Raji | IC50 |
572 molar ratio
Compound: glyzyrrhizin
|
Inhibition of TPA-induced EBV-early antigen activation in human Raji cells
Inhibition of TPA-induced EBV-early antigen activation in human Raji cells
|
[PMID: 16441065] |
| Raji | IC50 |
381 μM
Compound: 8
|
Inhibition of TPA-induced EBV-early antigen activation in human Raji cells after 48hrs by indirect immunofluorescence technique
Inhibition of TPA-induced EBV-early antigen activation in human Raji cells after 48hrs by indirect immunofluorescence technique
|
[PMID: 19131254] |
| RAW264.7 | ED50 |
70 μM
Compound: 1, GL
|
Inhibition of HMGB1 in mouse RAW264.7 cells assessed as LPS-induced TNFalpha release treated for 2 hrs prior to LPS-challenge measured after 16 hrs by ELISA
Inhibition of HMGB1 in mouse RAW264.7 cells assessed as LPS-induced TNFalpha release treated for 2 hrs prior to LPS-challenge measured after 16 hrs by ELISA
|
[PMID: 23199028] |
| RAW264.7 | IC50 |
20.7 μM
Compound: GL
|
Inhibition of NO release in mouse RAW264.7 cells incubated for 24 hrs by Griess reagent based assay
Inhibition of NO release in mouse RAW264.7 cells incubated for 24 hrs by Griess reagent based assay
|
[PMID: 37542990] |
| Vero | CC50 |
24000 μM
Compound: 51; GL
|
Cytotoxicity against African green monkey Vero cells
Cytotoxicity against African green monkey Vero cells
|
[PMID: 32845145] |
| Vero C1008 | CC50 |
>100 μM
Compound: 1; GL
|
Cytotoxicity against African green monkey Vero E6 cells assessed as reduction in survival rate measured after 48 hrs by MTT assay
Cytotoxicity against African green monkey Vero E6 cells assessed as reduction in survival rate measured after 48 hrs by MTT assay
|
[PMID: 31519375] |
| Vero C1008 | IC50 |
8.1 μM
Compound: 1; GL
|
Antiviral activity against DENV2 16681 infected in African green monkey Vero E6 cells assessed as inhibitory rate of NS4B positive cells measured after 96 hrs incubation by DAPI staining based immunofluorescence method
Antiviral activity against DENV2 16681 infected in African green monkey Vero E6 cells assessed as inhibitory rate of NS4B positive cells measured after 96 hrs incubation by DAPI staining based immunofluorescence method
|
[PMID: 31519375] |
| WI-38 | IC50 |
127.7 μM
Compound: GL
|
Cytotoxicity against human WI-38 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against human WI-38 cells assessed as inhibition of cell viability incubated for 24 hrs by MTT assay
|
[PMID: 37542990] |
Glycyrrhizic acid shows a series of anti-cancer-related pharmacological activities, such as broad-spectrum anti-cancer ability, resistance to the tissue toxicity caused by chemotherapy and radiation, drug absorption enhancing effects and anti-multidrug resistance (MDR) mechanisms, as a carrier material in drug delivery systems[1].
In intestinal NCI-H716 cells that secretes GLP-1, Glycyrrhizic acid promotes GLP-1 secretion with a marked elevation of calcium levels. Glycyrrhizic acid can enhance GLP-1 secretion through TGR5 activation[2].
Glycyrrhizic acid can form a stable transparent low-molecular-weight hydrogels (LMWHs) at 37°C in physiological phosphate buffered saline (PBS) with nanoclusters as the microstructures[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Glycyrrhizic acid (Glycyrrhizic acid; 50 mg/kg, i.p.) significantly decreases the levels of TgAb, HMGB1, TNF-α, IL-6, IL-1β in mice[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
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CAS No. 1405-86-3
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Appearance Solid
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Molecular Weight 822.93
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Formula C42H62O16
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Color White to off-white
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SMILES
C[C@]12[C@@](C(C=C3[C@]2(CC[C@]4(C)[C@@]3([H])C[C@](C(O)=O)(C)CC4)C)=O)([H])[C@@]5([C@@](C(C)([C@@H](O[C@]6([H])[C@@H]([C@H]([C@H](O)[C@@H](C(O)=O)O6)O)O[C@]7([H])O[C@@H]([C@@H](O)[C@H](O)[C@H]7O)C(O)=O)CC5)C)([H])CC1)C
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Synonyms
Glycyrrhizin
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Publications (59)
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Journal Impact Factor
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Most Recent
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Nat Nanotechnol
Tumour-derived microparticles obtained through microwave irradiation induce immunogenic cell death in lung adenocarcinoma. [Abstract]2025 May 19. PMID: 40389640 -
Adv Sci (Weinh)
Generation of Anti-Mastitis Gene-Edited Dairy Goats with Enhancing Lysozyme Expression by Inflammatory Regulatory Sequence using ISDra2-TnpB System. [Abstract]2024 Aug 5:e2404408. PMID: 39099401 -
Glycyrrhizic acid purchased from MedChemExpress. Usage Cited in: Chem Eng J. 2025 May 1.
The protein expression of P21, P16, Tom20, HMGB1, cGAS, and STING were assessed via western blotting with β-tubulin as a loading control. Data were expressed as mean ± SEM (n = 3). The results showed that Glycyrrhizic acid (10 μM; 24 h) significantly enhanced the anti-senescent effect of exosomes and inhibited the HMGB1/cGAS-STING axis.
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J Exp Clin Cancer Res
GPR65 sensing tumor-derived lactate induces HMGB1 release from TAM via the cAMP/PKA/CREB pathway to promote glioma progression. [Abstract]2024 Apr 4;43(1):105. PMID: 38576043
Glycyrrhizic acid purchased from MedChemExpress. Usage Cited in: J Exp Clin Cancer Res. 2024 Apr 4;43(1):105. [Abstract]
Glycyrrhizin (1 nM/kg; i.c.v.; administered every 3 days starting from day 14 after modeling). A, In a subcutaneous xenograft tumor model, the tumor volumes were measured and monitored every 7 days from each group of mice. (n = 4/group). B, The pictures of corresponding subcutaneous xenograft tumors dissected from each group mice at 42 days post-injection. C Tumor weights from each group at 42 days post-injection.
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Mater Today Bio
Glycyrrhizic acid-loaded biomimetic hybrid liposomes targeting inflammatory cascades and PD-1/PD-L1 pathway to reverse neuroinflammation-driven cognitive decline. [Abstract]2025 Dec 8:36:102657. PMID: 41476753 -
Mater Today Bio
Membrane biomimetic nanoenzyme-incorporated hybrid glycyrrhizic acid hydrogel for precise mitochondrial ROS scavenging for osteoarthritis treatment. [Abstract]2025 Apr 17:32:101778. PMID: 40290887 -
Adv Healthc Mater
Fn-HMGB1 Adsorption Behavior Initiates Early Immune Recognition and Subsequent Osteoinduction of Biomaterials. [Abstract]2024 Jan;13(2):e2301808. PMID: 37602504
Glycyrrhizic acid purchased from MedChemExpress. Usage Cited in: Adv Healthc Mater. 2024 Jan;13(2):e2301808. [Abstract]
Osteoinduction was hindered in Glycyrrhizic acid (GA, 10 mM; 30min) group.
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Cell Commun Signal
Neutrophil extracellular traps induced by the hypoxic microenvironment in gastric cancer augment tumour growth. [Abstract]2023 May 1;21(1):86. PMID: 37127629 -
Phytomedicine
Amoebicidal action of isoliquiritigenin and glabridin from Glycyrrhiza species: Mechanisms and effects against Acanthamoeba castellanii. [Abstract]2025 Sep:145:157081. PMID: 40701128 -
Phytomedicine
Bioactive equivalent combinatorial components of Xiao-Xu-Ming decoction inhibit the calmodulin-mediated MLCK/MLC axis to attenuate coronary artery spasm. [Abstract]2025 Jul:142:156713. PMID: 40349422 -
Phytomedicine
Glycyrrhizin alleviates the toxicity of hydroxychloroquine in treating oral lichen planus by occupying heat shock protein 90 alpha. [Abstract]2024 Dec:135:156059. PMID: 39550918
Glycyrrhizic acid purchased from MedChemExpress. Usage Cited in: Phytomedicine. 2024 Dec:135:156059. [Abstract]
qRT-PCR analysis of HSP90AB1 and HSP90AA1 in NOK cells after stimulation with LPS and HCQ (10 µM) or Glycyrrhiz (GL, 100 μg/mL) in for 24 h.
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Food Res Int
Glycyrrhiza uralensis Fisch: A novel source of analgesic activity through NaV1.8 sodium channel modulation. [Abstract]2025 Dec;222(Pt 1):117620. PMID: 41267240 -
Redox Rep
Monoammonium glycyrrhizinate ameliorates mitochondrial dysfunction-mediated oxidative stress and neuroinflammation via the NRF2/NQO1 axis after spinal cord injury. [Abstract]2025 Dec;30(1):2585221. PMID: 41240391 -
Cell Death Discov
2024 Jan 17;10(1):34. PMID: 38233385 -
EMBO Rep
Aspergillus fumigatus promotes tumor angiogenesis via SLC7A11 on myeloid-derived suppressor cells. [Abstract]2025 Nov 17. PMID: 41249582 -
Cell Prolif
2024 Nov 20:e13774. PMID: 39566909 -
Cell Prolif
TNF-α/HMGB1 inflammation signalling pathway regulates pyroptosis during liver failure and acute kidney injury. [Abstract]2020 Jun;53(6):e12829. PMID: 32419317
Glycyrrhizic acid purchased from MedChemExpress. Usage Cited in: Cell Prolif. 2020 Jun;53(6):e12829. [Abstract]
Protein levels of pro-caspase-1 + p10 + p12, GADMD, IL-1β, IL-18 and NLRP3 are detected by Western blotting. Glycyrrhizin inhibits pyroptosis in TNF-α-induced M1 macrophages.
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Drug Des Devel Ther
The Jieduan-Niwan Formula Reduces Inflammatory Responses in Acute-on-Chronic Liver Failure Rats by Inhibiting HMGB1-Induced Hepatocyte Pyroptosis. [Abstract]2025 Apr 2:19:2503-2517. PMID: 40190810 -
CNS Neurosci Ther
11,12-Diacetyl-Carnosol Ameliorates Depression-Like Behaviors and Memory Dysfunction in CUMS Mouse Model via Inhibiting HMGB1-Mediated Neuroinflammation. [Abstract]2025 May;31(5):e70406. PMID: 40406924 -
Pharmaceuticals (Basel)
Bruceine D Identified as a Drug Candidate against Breast Cancer by a Novel Drug Selection Pipeline and Cell Viability Assay. [Abstract]2022 Jan 31;15(2):179. PMID: 35215292 -
Pharm Biol
Sesamin attenuates intestinal injury in sepsis via the HMGB1/TLR4/IL-33 signalling pathway. [Abstract]2020 Dec;58(1):898-904. PMID: 32893702 -
Eur J Pharmacol
HBHP ameliorates CCL4-induced liver fibrosis in rats by inhibiting HMGB1-mediated inflammatory response through binding to the HMGB1-A box. [Abstract]2025 Oct 5:1004:177971. PMID: 40683441 -
Int Immunopharmacol
Glycyrrhizin alleviates brain injury in necrotizing enterocolitis model mice by suppressing HMGB1/TLR4 pathway. [Abstract]2025 Mar 26:150:114294. PMID: 39970710 -
Int Immunopharmacol
Inhibiting HMGB1/AGER/NF-κB pathway prevents pro-inflammatory microglia polarization and protect photoreceptors in retinitis pigmentosa. [Abstract]2025 Feb 3:149:114192. PMID: 39904032 -
Neuropharmacology
Zinc induces neuronal autophagy via HMGB1 nuclear translocation in acute cerebral ischemia. [Abstract]2025 Nov 15:279:110617. PMID: 40752584 -
Hepatol Commun
Aging aggravates liver fibrosis through downregulated hepatocyte SIRT1-induced liver sinusoidal endothelial cell dysfunction. [Abstract]2023 Dec 22;8(1):e0350. PMID: 38126919 -
Rheumatology (Oxford)
Autophagy inhibitors block pathogenic NET release in immune-mediated inflammatory disease without impairing host defence. [Abstract]2025 Aug 13:keaf437. PMID: 40802538 -
Mol Neurobiol
Glycyrrhizin Attenuates White Matter Injury by Inhibiting Neuroinflammation through the HMGB1/TLR4 Pathway. [Abstract]2025 May;62(5):6070-6087. PMID: 39707121 -
Front Cell Dev Biol
Nucleotide-Binding Oligomerization Domain-Like Receptor 3 Deficiency Attenuated Isoproterenol-Induced Cardiac Fibrosis via Reactive Oxygen Species/High Mobility Group Box 1 Protein Axis. [Abstract]2020 Aug 11;8:713. PMID: 32850832 -
J Cell Mol Med
Jinbei Decoction Attenuates LPS-Induced Acute Lung Injury via Suppression of TRAF6-Dependent Inflammatory Response in Macrophage. [Abstract]2025 Nov;29(21):e70944. PMID: 41230791 -
Mediators Inflamm
HMGB1 Exacerbates Intestinal Barrier Damage by Inducing Ferroptosis Through the TLR4/NF-κB/GPX4 Pathway in Ulcerative Colitis. [Abstract]2025 Jul 11:2025:2395557. PMID: 40689397 -
J Inflamm Res
HMGB1 Inhibition Alleviates Chronic Nonbacterial Prostatitis by Suppressing M1 Polarization of Macrophages. [Abstract]2025 May 25:18:6735-6748. PMID: 40453963 -
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Sci Rep
Xiaoyao San against depression via glia-mediated neuroinflammation using network pharmacology and experimental validation. [Abstract]2025 Nov 12;15(1):39708. PMID: 41225027 -
Fish Shellfish Immunol
Grass carp Il-2 promotes neutrophil extracellular traps formation via inducing ROS production and autophagy in vitro. [Abstract]2024 Jan:144:109261. PMID: 38040137 -
ACS Chem Neurosci
Alarmin HMGB1 Plays a Detrimental Role in Hippocampal Dysfunction Caused by Hypoxia-Ischemia Insult in Neonatal Mice: Evidence from the Application of the HMGB1 Inhibitor Glycyrrhizin. [Abstract]2020 Mar 18;11(6):979-993. PMID: 32073822 -
Aging (Albany NY)
2019 Jul 7;11(13):4323-4337. PMID: 31284269 -
Cell Signal
Glycyrrhizic acid alleviated MI/R-induced injuries by inhibiting Hippo/YAP signaling pathways. [Abstract]2024 Mar:115:111036. PMID: 38185229 -
Eur J Med Res
HMGB1 regulates autophagy via TLR4/NF-κB signaling pathway in myocardial injury induced by coronary microembolization. [Abstract]2025 Oct 9;30(1):943. PMID: 41068984 -
Cardiovasc Drugs Ther
High Mobility Group Protein B1 Mediates the Role of the Neutrophil Extracellular Traps in the Progression of Acute Myocardial Infarction. [Abstract]2026 Jan 24. PMID: 41579229 -
3 Biotech
Lycorine attenuates lipopolysaccharide-induced acute lung injury through the HMGB1/TLRs/NF-κB pathway. [Abstract]2020 Aug;10(8):369. PMID: 32818131 -
Vet Microbiol
The Chinese medicine monomer Schisandrin C inhibits PRRSV infection by regulating the OGT-PI3K/AKT/mTOR signaling pathway. [Abstract]2026 May:316:110992. PMID: 41865607 -
Toxicol In Vitro
The protective mechanisms of glycyrrhizic acid for deoxynivalenol-induced toxicity in rabbit corneal stroma. [Abstract]2025 Oct:108:106104. PMID: 40617304 -
BMC Immunol
Glycyrrhizin improves the pathogenesis of psoriasis partially through IL-17A and the SIRT1-STAT3 axis. [Abstract]2021 May 27;22(1):34. PMID: 34044769 -
Adv Biol (Weinh)
HMGB1 Derived from the Pyroptotic Microenvironment Promotes Macrophage Extracellular Traps in Hirschsprung-Associated Enterocolitis. [Abstract]2025 Jun 4:e00761. PMID: 40464207 -
Behav Brain Res
HMGB1/RAGE signaling mediates the activation of microglia and participates in depressive-like behaviors and cognitive deficits in rats after ischemia-reperfusion. [Abstract]2025 May 24:115662. PMID: 40419119 -
Biochem Biophys Res Commun
Uric acid inhibits HMGB1-TLR4-NF-κB signaling to alleviate oxygen-glucose deprivation/reoxygenation injury of microglia. [Abstract]2021 Feb 12:540:22-28. PMID: 33429196 -
World Neurosurg
Glycyrrhizic Acid Attenuates the Inflammatory Response After Spinal Cord Injury by Inhibiting High Mobility Group Box-1 Protein Through the p38/Jun N-Terminal Kinase Signaling Pathway. [Abstract]2022 Feb:158:e856-e864. PMID: 34838764 -
Planta Med
Compound Cocktail Inhibits Influenza Viral Pneumonia via Phospholipase Cγ1 Phosphorylation-Related Necroptosis and Partial Autophagy in Natural Killer Cells. [Abstract]2021 Jun;87(7):538-549. PMID: 33545719 -
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Evid Based Complement Alternat Med
Glycyrrhizin Ameliorates Radiation Enteritis in Mice Accompanied by the Regulation of the HMGB1/TLR4 Pathway. [Abstract]2020 May 31;2020:8653783. PMID: 32595744
Solvent & Solubility
DMSO : 100 mg/mL (121.52 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
H2O : < 0.1 mg/mL (insoluble)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (3.04 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (3.04 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Protocol
Mice[3]
NOD.H-2h4 mice are fed in the animal house until 4 weeks of age. A total of 24 male mice are then randomly separated into three different groups (n=8 per group). Mice in the control group are given sterile water without supplement. Mice in the iodine supplement (NaI) group are given 0.005% NaI in the drinking water. Mice in the NaI+Glycyrrhizic acid group are treated with 50 mg/kg Glycyrrhizic acid once daily for 4 weeks, administered via intraperitoneal injection after 8 weeks of iodine supplementation. Thyroid tissues are removed surgically under anesthesia, washed with cold saline, blotted on filter paper and weighed using an electronic balance. The thyroid gland tissues are then stored at -80°C until use[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Purity & Documentation
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Data Sheet (283 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
[1]. Su X, et al. Glycyrrhizic acid: A promising carrier material for anticancer therapy. Biomed Pharmacother. 2017 Sep 5;95:670-678 [Content Brief]
[2]. Wang LY, et al. Glycyrrhizic acid increases glucagon like peptide-1 secretion via TGR5 activation in type 1-like diabetic rats. Biomed Pharmacother. 2017 Sep 4;95:599-604. [Content Brief]
[3]. Li C, et al. Glycyrrhizin, a Direct HMGB1 Antagonist, Ameliorates Inflammatory Infiltration in a Model of Autoimmune Thyroiditis via Inhibition of TLR2-HMGB1 Signaling. Thyroid. 2017 May;27(5):722-731. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 1.2152 mL | 6.0759 mL | 12.1517 mL | 30.3793 mL |
| 5 mM | 0.2430 mL | 1.2152 mL | 2.4303 mL | 6.0759 mL | |
| 10 mM | 0.1215 mL | 0.6076 mL | 1.2152 mL | 3.0379 mL | |
| 15 mM | 0.0810 mL | 0.4051 mL | 0.8101 mL | 2.0253 mL | |
| 20 mM | 0.0608 mL | 0.3038 mL | 0.6076 mL | 1.5190 mL | |
| 25 mM | 0.0486 mL | 0.2430 mL | 0.4861 mL | 1.2152 mL | |
| 30 mM | 0.0405 mL | 0.2025 mL | 0.4051 mL | 1.0126 mL | |
| 40 mM | 0.0304 mL | 0.1519 mL | 0.3038 mL | 0.7595 mL | |
| 50 mM | 0.0243 mL | 0.1215 mL | 0.2430 mL | 0.6076 mL | |
| 60 mM | 0.0203 mL | 0.1013 mL | 0.2025 mL | 0.5063 mL | |
| 80 mM | 0.0152 mL | 0.0759 mL | 0.1519 mL | 0.3797 mL | |
| 100 mM | 0.0122 mL | 0.0608 mL | 0.1215 mL | 0.3038 mL |