Saponarin
(Synonyms: 皂草甙) 目录号 : GC64119
A flavonoid glycoside with diverse biological activities
Cas No.:20310-89-8
Sample solution is provided at 25 µL, 10mM.
Saponarin is a flavonoid glycoside that has been found in H. vulgare and has diverse biological activities.1,2,3,4 It prevents UV- or Fenton’s reagent-induced lipid peroxidation in cell-free assays.1 Saponarin (50 and 100 ?M) increases intracellular calcium concentrations and induces AMPK phosphorylation in HepG2 and TE 671 cells, as well as increases glucose uptake and reduces glucose production in HepG2 cells.2 It inhibits the LPS-induced production of TNF-α and IL-1β in RAW 264.7 cells and induces the expression of skin barrier genes encoding hyaluronan synthase-3, aquaporin-3, and the antimicrobial peptide LL-37 in HaCaT cells.3 In vivo, saponarin (80 mg/kg, p.o) reduces cocaine-induced production of thiobarbituric acid reactive substances (TBARS), decreases in hepatic levels of catalase, superoxide dismutase (SOD), and glutathione peroxidase (GPX), and hepatotoxicity in rats.4
1.Kamiyama, M., and Shibamoto, T.Flavonoids with potent antioxidant activity found in young green barley leavesJ. Agric. Food Chem.60(25)6260-6267(2012) 2.Seo, W.-D., Lee, J.H., Jia, Y., et al.Saponarin activates AMPK in a calcium-dependent manner and suppresses gluconeogenesis and increases glucose uptake via phosphorylation of CRTC2 and HDAC5Bioorg. Med. Chem. Lett.25(22)5237-5242(2015) 3.Min, S.-Y., Park, C.-H., Yu, H.-W., et al.Anti-inflammatory and anti-allergic effects of saponarin and its impact on signaling pathways of RAW 264.7, RBL-2H3, and HaCaT cellsInt. J. Mol. Sci.22(16)8431(2021) 4.Vitcheva, V., Simeonova, R., Krasteva, I., et al.Hepatoprotective effects of saponarin, isolated from Gypsophila trichotoma Wend. on cocaine-induced oxidative stress in ratsRedox Rep.16(2)56-61(2011)
Cas No. | 20310-89-8 | SDF | Download SDF |
别名 | 皂草甙 | ||
分子式 | C27H30O15 | 分子量 | 594.52 |
溶解度 | DMSO : 100 mg/mL (168.20 mM; Need ultrasonic) | 储存条件 | 4°C, away from moisture and light |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
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1 mg | 5 mg | 10 mg |
1 mM | 1.682 mL | 8.4101 mL | 16.8203 mL |
5 mM | 0.3364 mL | 1.682 mL | 3.3641 mL |
10 mM | 0.1682 mL | 0.841 mL | 1.682 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet