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CIL56

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纯度: 99.91%

货号 T4309Cas号 300802-28-2

别名 CA3

CIL56 (CA3) 是一种选择性铁死亡诱导剂,可通过产生铁依赖性活性氧来诱导细胞铁死亡。

CIL56
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CIL56

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Rating icon 很棒

纯度: 99.91%

货号 T4309 别名 CA3Cas号 300802-28-2

CIL56 (CA3) 是一种选择性铁死亡诱导剂,可通过产生铁依赖性活性氧来诱导细胞铁死亡。

规格价格库存数量
1 mg
¥ 240
现货
2 mg
¥ 351
现货
5 mg
¥ 609
现货
10 mg
¥ 950
现货
25 mg
¥ 1,570
现货
50 mg
¥ 2,560
现货
100 mg
¥ 3,930
现货
1 mL x 10 mM (in DMSO)
¥ 642
现货
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产品介绍


CIL56 AI Summary
CIL56 exhibits a wide range of bioactivities, making it a versatile compound for potential drug development and research. Its bioactivities include inhibition of Luciferase Translation or Activity in H4 Neuroglioblastoma Cells, modulation of Lamin A Splicing, and inhibition of HSD17B4 and Human Jumonji Domain Containing 2E (JMJD2E). Additionally, it acts as a modulator of miRNAs and/or activator of miR-21, enhances SMN2 Splice Variant Expression, and serves as an agonist of the Thyroid Stimulating Hormone Receptor. CIL56 also inhibits Tyrosyl-DNA Phosphodiesterase (TDP1) and Heat Shock Factor 1 (HSF1), as well as various enzymes such as Aldehyde Dehydrogenase 1, HPGD, DNA Polymerase Beta. It inhibits ROR gamma transcriptional activity, T-Type Calcium Channel, and ATXN expression, induces DNA re-replication in various cell lines, and inhibits the Hepatitis C Virus (HCV) and various cellular signaling pathways. Notably, CIL56 inhibits Wnt/beta-catenin transcriptional activity in human HT-29 cells with an IC50 value of 990.0 nM, as assessed by TCF luciferase promoter reporter assay. It also shows cytotoxicity against human BJeLR cells overexpressing oncogenic RAS, though with an IC50 value greater than 1000.0 nM. These diverse bioactivities indicate that CIL56 has the potential for affecting numerous cellular processes and pathways, warranting further investigation for therapeutic applications..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
CIL56 (CA3) is a small molecule that induces cellular ferroptosis through the production of iron-dependent reactive oxygen species (ROS). It also induces accumulation of long-chain saturated, monounsaturated, and polyunsaturated fatty acids in HT-1080 cells in vitro.HT-1080 cells lacking acetyl-CoA carboxylase 1 (ACC1), the rate-limiting enzyme in fatty acid synthesis, exhibit 5-fold resistance to CIL56 treatment, indicating ACC1 activity sensitizes cells to CIL56-induced cell death.
别名CA3
化学信息
分子量489.61
分子式C23H27N3O5S2
CAS No.300802-28-2
SmilesON=C1c2cc(ccc2-c2ccc(cc12)S(=O)(=O)N1CCCCC1)S(=O)(=O)N1CCCCC1
密度1.51 g/cm3 (Predicted)
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 6.94 mg/mL (14.17 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM2.0424 mL10.2122 mL20.4244 mL102.1221 mL
5 mM0.4085 mL2.0424 mL4.0849 mL20.4244 mL
10 mM0.2042 mL1.0212 mL2.0424 mL10.2122 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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