Ginsenoside Rh7
(Synonyms: 人参皂苷RH7) 目录号 : GC61629GinsenosideRh7是一种从人参叶片中分离出的次要皂苷。
Cas No.:343780-68-7
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >96.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Ginsenoside Rh7 is a minor saponin isolated from the leaves of Panax ginseng[1].
[1]. D Q Dou, et al. Six New Dammarane-Type Triterpene Saponins From the Leaves of Panax Ginseng. Chem Pharm Bull (Tokyo). 2001 Apr;49(4):442-6.
Cas No. | 343780-68-7 | SDF | |
别名 | 人参皂苷RH7 | ||
Canonical SMILES | C[C@]12[C@]3([C@@]([C@H](O)C[C@]1([H])[C@@]4(C(C(C)([C@@H](O)CC4)C)=C[C@@H]2O)C)([H])[C@]([C@@](CC/C=C(C)/C)(C)O[C@@H]5O[C@@H]([C@@H](O)[C@H](O)[C@H]5O)CO)([H])CC3)C | ||
分子式 | C36H60O9 | 分子量 | 636.86 |
溶解度 | 储存条件 | Store at -20°C | |
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 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 1.5702 mL | 7.851 mL | 15.702 mL |
5 mM | 0.314 mL | 1.5702 mL | 3.1404 mL |
10 mM | 0.157 mL | 0.7851 mL | 1.5702 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。
Ginsenoside Rh7 Suppresses Proliferation, Migration and Invasion of NSCLC Cells Through Targeting ILF3-AS1 Mediated miR-212/SMAD1 Axis
Front Oncol 2021 Apr 29;11:656132.PMID:33996578DOI:10.3389/fonc.2021.656132.
It is reported that ginsenosides have a significant anti-tumor effect on a variety of tumors. However, the role and mechanism of Rh7 in non-small cell lung cancer (NSCLC) are unclear. In this study, we aimed to study the anti-tumor effect of Rh7 on the proliferation and progression of NSCLC. Bioinformatics analysis showed that ILF3-AS1 was regulated by Ginsenoside Rh7 in NSCLC. Down-regulation of ILF3-AS1 could significantly inhibit the proliferation, metastasis and invasion of NSCLC. In addition, ILF3-AS1 negatively controlled miR-212, which in turn targeted SMAD1 expression, thereby regulating NSCLC cell viability and apoptosis. Our results indicate that ILF3-AS1 can be used as a diagnostic and therapeutic target for non-small cell lung cancer. It is discovered for the first time that Ginsenoside Rh7 inhibits the expression of ILF3-AS1 and exerts antitumor effects.