E17241
(Synonyms: 4-(1,3-Dithiolan-2-yl)-N-(3-hydroxypyridin-2-yl)benzamide) 目录号 : GC91933E17241是编码ATP结合盒转运蛋白1的基因ABCA1表达的诱导剂;亚家族A(ABCA1)。
Cas No.:1060968-92-4
Sample solution is provided at 25 µL, 10mM.
E17241 is an inducer of the expression of ABCA1, the gene encoding ATP-binding cassette transporter 1; subfamily A (ABCA1).1 It induces the expression of ABCA1 in a reporter assay using HepG2 cells (EC50 = 280 nM). E17241 is also an agonist of peroxisome proliferator-activated receptors (PPARs).2 It induces PPAR-mediated gene expression in reporter assays using HepG2 cells expressing PPARγ, PPARα, or PPARδ (EC50s = 290, 3,900, and 879 nM, respectively). It increases the protein levels of ACBA1 in RAW 264.7 macrophages but not in the presence of siRNA targeting mRNA encoding PKCζ.1 E17241 (0.4, 2, or 10 ?M) increases cholesterol efflux in RAW 264.7 cells. It reduces plasma levels of cholesterol, alanine transaminase (ALT), and aspartate aminotransferase (AST) and hepatic levels of cholesterol and triglycerides, as well as decreases aortic lesion area, in an ApoE-/- mouse model of atherosclerosis when administered at a dose of 25 mg/kg. E17241 (50 mg/kg per day) decreases plasma glucose levels and body weight in KKAy diabetic mice fed a high-fat and high-glucose (HFHG) diet.2
References:
[1]. Xu, Y., Liu, C., Hang, X., et al.E17241 as a novel ABCA1 (ATP-binding cassette transporter A1) upregulator ameliorates atherosclerosis in miceArterioscler. Thromb. Vasc. Biol.41(6)e284-e298(2021).
[2]. Sheng, R., Li, Y., Wu, Y., et al.A pan-PPAR agonist E17241 ameliorates hyperglycemia and diabetic dyslipidemia in KKAy mice via up-regulating ABCA1 in islet, liver, and white adipose tissueBiomed. Pharmacother.172116200(2024).
Cas No. | 1060968-92-4 | SDF | |
别名 | 4-(1,3-Dithiolan-2-yl)-N-(3-hydroxypyridin-2-yl)benzamide | ||
化学名 | 4-(1,3-dithiolan-2-yl)-N-(3-hydroxypyridin-2-yl)benzamide | ||
Canonical SMILES | OC1=CC=CN=C1NC(C(C=C2)=CC=C2C3SCCS3)=O | ||
分子式 | C15H14N2O2S2 | 分子量 | 318.4 |
溶解度 | DMSO: Soluble: ≥10 mg/ml | 储存条件 | -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。 |
||
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 | 3.1407 mL | 15.7035 mL | 31.407 mL |
5 mM | 0.6281 mL | 3.1407 mL | 6.2814 mL |
10 mM | 0.3141 mL | 1.5704 mL | 3.1407 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: >95.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet