货号:A458176
同义名:
Q-100692; KB-289522
Glabridin是一种天然产物,从甘草根部提取和纯化,具有多种生物学功能,如在高葡萄糖水平下调节iNOS的合成和活性,显著抑制代谢中产生的自由基,保护抗氧化敏感的生物大分子(如LDL、DNA)和细胞壁,具有美白和抗衰老活性。


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| 产品名称 | PPARα ↓ ↑ | PPARβ/δ ↓ ↑ | PPARγ ↓ ↑ | PPARδ ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Fenofibric acid | ✔ | 98% | |||||||||||||||||
| GW6471 |
++
PPARα, IC50: 0.24 μM |
99%+ | |||||||||||||||||
| GSK3787 |
++
PPARδ, pIC50: 6.6 |
++
PPARδ, pIC50: 6.6 |
99%+ | ||||||||||||||||
| FH535 | ✔ | 98%+ | |||||||||||||||||
| GW9662 |
+++
PPARα, IC50: 32 nM |
+++
PPARγ, IC50: 3.3 nM |
98% | ||||||||||||||||
| T0070907 |
++++
PPARγ, IC50: 1 nM |
98% | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | Glabridin, a compound in the root extract of Glycyrrhiza glabra, as an effective tyrosinase inhibitor. Glabridin applied on skin can inhibit melanin synthesis[3]. Glabridin significantly inhibited migration/invasion capacities of HCC cells, Huh7 and Sk-Hep-1[6]. Glabridin-induced cell apoptosis in HL-60 and MV4-11 cells[7]. Glabridin also upregulated the expression of miR-148a in a dose-dependent manner and attenuated angiogenesis in two human breast cancer cell lines (MDA-MB-231 and Hs-578T)[5]. Glabridin((10 or 50 mg/kg/day) ) could ameliorate dextran sulphate sodium (DSS)-induced colitis[8]. |
| Concentration | Treated Time | Description | References | |
| Peripheral blood mononuclear cells (PBMCs) | 20 μM | 1 hour | Glabridin effectively inhibited the activation of IRF3 in PBMCs and reduced the expression of IFN-β, IL-6, and TNF-α. | Mol Med. 2023 Dec 8;29(1):167 |
| Bone-marrow-derived macrophages (BMDMs) | 20 μM | 1 hour | Glabridin significantly inhibited the activation of STING and IRF3 in BMDMs and reduced the expression of IFN-β, IL-6, and TNF-α. | Mol Med. 2023 Dec 8;29(1):167 |
| RAW264.7 cells | 10 μM and 20 μM | 24 hours | To evaluate the anti-inflammatory effect of GLA, results showed that GLA significantly inhibited NO secretion by macrophages. | Adv Sci (Weinh). 2025 May;12(18):e2407802 |
| Peripheral blood mononuclear cells (PBMCs) | 20 μM | 1 hour | To verify the broad-spectrum inhibitory effect of Glabridin on the cGAS-STING signaling pathway. Results showed that Glabridin effectively inhibited cGAMP and diABZI-induced IRF3 activation and reduced the gene expression of IFN-β, IL-6, and TNF-α. | Mol Med. 2023 Dec 8;29(1):167 |
| Bone-marrow-derived macrophages (BMDMs) | 20 μM | 1 hour | To evaluate the effect of Glabridin on the cGAS-STING signaling pathway. Results showed that Glabridin significantly inhibited HT-DNA-induced activation of STING and IRF3, and reduced the gene expression of IFN-β, IL-6, and TNF-α. | Mol Med. 2023 Dec 8;29(1):167 |
| T. gondii RH strain tachyzoites | 5 µg/ml | 24 and 48 hours | To evaluate the inhibitory effects of glabridin on T. gondii tachyzoites, results showed significant inhibition of proliferation and invasion, along with structural damage. | Parasit Vectors. 2024 Dec 18;17(1):522 |
| Vero cells | 5 µg/ml | 24 hours | To evaluate the cytotoxicity of glabridin on Vero cells, results showed 99.05% cell viability at 5 µg/ml with no significant toxicity. | Parasit Vectors. 2024 Dec 18;17(1):522 |
| Human platelets | 5–30 µM | 3 minutes | Inhibited collagen-induced platelet aggregation | Chin Med. 2023 Jun 10;18(1):71 |
| Human cutaneous T-cell lymphoma cell line H9 | 0, 2.5, 5, 10, 20, 40, 80 μM | 24 hours | To evaluate the effect of Glabridin on CTCL cell viability, results showed that Glabridin significantly inhibits cell viability and induces programmed cell death (apoptosis, autophagy, and necrosis). | Cell Prolif. 2024 Sep;57(9):e13701 |
| Human cutaneous T-cell lymphoma cell line HH | 0, 2.5, 5, 10, 20, 40, 80 μM | 24 hours | To evaluate the effect of Glabridin on CTCL cell viability, results showed that Glabridin significantly inhibits cell viability and induces programmed cell death (apoptosis, autophagy, and necrosis). | Cell Prolif. 2024 Sep;57(9):e13701 |
| Human platelets | 20 and 30 µM | 3 minutes | Inhibited phosphorylation of Lyn, Fyn, Syk, and integrin β3 | Chin Med. 2023 Jun 10;18(1):71 |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6J mice | Trex1-deficient mice | Intraperitoneal injection | 40 mg/kg | Daily for 14 days | Glabridin significantly alleviated the inflammatory response in Trex1-deficient mice and reduced the expression of IFN-β, CXCL10, ISG15, IL-6, and TNF-α in various tissues. | Mol Med. 2023 Dec 8;29(1):167 |
| C57BL/6J mice | DMXAA-induced cGAS-STING signaling pathway activation model | Intraperitoneal injection | 20 or 40 mg/kg | Single injection, lasting 4 hours | To study the inhibitory effect of Glabridin on the cGAS-STING signaling pathway in vivo. Results showed that Glabridin significantly reduced the levels of IFN-β, IL-6, and TNF-α in serum and peritoneal lavage fluid induced by DMXAA. | Mol Med. 2023 Dec 8;29(1):167 |
| Sprague-Dawley rats | High-fat diet combined with streptozotocin-induced diabetic nephropathy model | Intraperitoneal injection | 50 mg/kg | Once daily for 28 consecutive days | To investigate the protective effect of Glabridin on diabetic nephropathy in rats, results showed that Glabridin could improve renal function, alleviate renal pathological changes, inhibit oxidative stress and ferroptosis, and exert its effects by regulating the VEGF/Akt/ERK pathway. | Mol Med. 2022 May 20;28(1):58 |
| BALB/c mice | T. gondii RH strain infection model | Oral gavage | 50 mg/kg and 100 mg/kg | 7 consecutive days | To evaluate the effect of glabridin on the survival rate of T. gondii-infected mice, results showed that 100 mg/kg dose significantly prolonged survival time, with 20% of mice surviving until day 25 post-infection. | Parasit Vectors. 2024 Dec 18;17(1):522 |
| ICR mice | Acute pulmonary thromboembolism model | Intraperitoneal injection | 6 and 12 mg/kg | Single dose | Reduced thrombus formation in lung vessels | Chin Med. 2023 Jun 10;18(1):71 |
| 计算器 | ||||
| 存储液制备 | ![]() |
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 |
|
| CAS号 | 59870-68-7 |
| 分子式 | C20H20O4 |
| 分子量 | 324.37 |
| SMILES Code | OC1=CC=C([C@H]2CC3=CC=C4C(C=CC(C)(C)O4)=C3OC2)C(O)=C1 |
| MDL No. | MFCD03427694 |
| 别名 | Q-100692; KB-289522; LS-176045 |
| 运输 | 蓝冰 |
| InChI Key | LBQIJVLKGVZRIW-ZDUSSCGKSA-N |
| Pubchem ID | 124052 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 25 mg/mL(77.07 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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