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Glabridin/光甘草定 {[allProObj[0].p_purity_real_show]}

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。

Glabridin/光甘草定 化学结构 CAS号:59870-68-7
Glabridin/光甘草定 化学结构
CAS号:59870-68-7
Glabridin/光甘草定 3D分子结构
CAS号:59870-68-7
Glabridin/光甘草定 化学结构 CAS号:59870-68-7
Glabridin/光甘草定 3D分子结构 CAS号:59870-68-7
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Glabridin/光甘草定 纯度/质量文件 产品仅供科研

货号:A458176 标准纯度: {[allProObj[0].p_purity_real_show]}
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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。

Glabridin/光甘草定 生物活性

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].

Glabridin/光甘草定 细胞实验

Cell Line
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

Glabridin/光甘草定 动物实验

Species
Animal Model
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

Glabridin/光甘草定 参考文献

[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.

Glabridin/光甘草定 实验方案

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

Glabridin/光甘草定 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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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