(20S)-Protopanaxatriol
(Synonyms: 20 (S)-原人参三醇; 20(S)-APPT; g-PPT) 目录号 : GC34965An active ginsenoside metabolite
Cas No.:34080-08-5
Sample solution is provided at 25 µL, 10mM.
20(S)-Protopanaxatriol is an active aglycone metabolite of various panaxatriol ginsenosides, including ginsenoside Re , ginsenoside Rf , ginsenoside Rg1 , ginsenoside Rg2 , and ginsenoside Rh1 .1 It is cytotoxic to HL-60 cancer cells (IC50 = 16 ?M).2 20(S)-Protopanaxatriol inhibits the proliferation of human umbilical vein endothelial cells (HUVECs; EC50 = 6.64 ?g/ml).3 It inhibits LPS-induced increases in the protein levels of COX-2 and inducible nitric oxide synthase (iNOS) and decreases LPS-induced NF-κB activity in RAW 264.7 cells when used at concentrations ranging from 1 to 20 ?M.4
1.Helms, S.Cancer prevention and therapeutics: Panax ginsengAltern. Med. Rev.9(3)259-274(2004) 2.Tian, Y., Guo, H., Han, J., et al.Microbial transformation of 20(S)-protopanaxatriol by Mucor spinosusJ. Nat. Prod.68(5)678-680(2005) 3.Usami, Y., Liu, Y.-N., Lin, A.-S., et al.Antitumor agents. 261. 20(S)-Protopanaxadiol and 20(s)-protopanaxatriol as antiangiogenic agents and total assignment of 1H NMR spectraJ. Nat. Prod.71(3)478-481(2008) 4.Oh, G.S., Pae, H.O., Choi, B.M., et al.20(S)-Protopanaxatriol, one of ginsenoside metabolites, inhibits inducible nitric oxide synthase and cyclooxygenase-2 expressions through inactivation of nuclear factor-κB in RAW 264.7 macrophages stimulated with lipopolysaccharideCancer Lett.205(1)23-29(2004)
Cas No. | 34080-08-5 | SDF | |
别名 | 20 (S)-原人参三醇; 20(S)-APPT; g-PPT | ||
Canonical SMILES | C[C@]([C@@](C[C@H]1O)([H])[C@]2(CC[C@@H]3O)C)(C[C@H](O)[C@@]2([H])C3(C)C)[C@]4([C@@]1([H])[C@]([C@@](C)(O)CC/C=C(C)/C)([H])CC4)C | ||
分子式 | C30H52O4 | 分子量 | 476.73 |
溶解度 | DMSO: 100 mg/mL (209.76 mM) | 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 | 2.0976 mL | 10.4881 mL | 20.9762 mL |
5 mM | 0.4195 mL | 2.0976 mL | 4.1952 mL |
10 mM | 0.2098 mL | 1.0488 mL | 2.0976 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
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- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet