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Cystamine dihydrochloride

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纯度: 99.81%

货号 T20109Cas号 56-17-7

别名 胱胺二盐酸盐

Cystamine dihydrochloride 是一种辐射防护剂。它还可以防止四氯化碳肝损伤。

Cystamine dihydrochloride
其他形式的 “Cystamine dihydrochloride”:

Cystamine dihydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.81%

货号 T20109 别名 胱胺二盐酸盐Cas号 56-17-7

Cystamine dihydrochloride 是一种辐射防护剂。它还可以防止四氯化碳肝损伤。

规格价格库存数量
10 g
¥ 278
现货
1 mL x 10 mM (in DMSO)
¥ 195
现货
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产品介绍


Cystamine dihydrochloride AI Summary
Cystamine dihydrochloride exhibits a range of bioactivities, including potent inhibition of the proliferation of Plasmodium falciparum line 3D7 with an IC50 of 8912.5 nM. It serves as an inhibitor of Tyrosyl-DNA Phosphodiesterase (TDP1) with IC50 values of 28183.8 nM and 1778.3 nM. Additionally, Cystamine dihydrochloride inhibits Tau Fibril Formation, with potencies between 12589.3 nM and 14125.4 nM. It is also effective as a cell-membrane permeable IMPase inhibitor, showing potency at 5623.4 nM. Furthermore, the compound displays inhibitory activities on Fructose-1,6-bisphosphate Aldolase, MPP8 Chromodomain Interactions, Histone Lysine Methyltransferase G9a, vitamin D receptor (VDR), Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1), and Marburg Virus entry, with potencies spanning from 44.7 nM to 79432.8 nM. In terms of transporter interactions, Cystamine dihydrochloride strongly inhibits sodium fluorescein uptake, demonstrating an 89.2% inhibition in OATP1B3-transfected CHO cells and 111.28% in OATP1B1-transfected CHO cells at a 10 µM concentration, indicating its capacity to interfere with the transport mechanisms mediated by these transporters. Additionally, Cystamine dihydrochloride acts as an inhibitor of histone lysine methyltransferases G9a with an IC50 of 15000.0 nM, albeit showing weaker inhibition of GLP, with an IC50 greater than 100000.0 nM. It also has a weak to negligible inhibitory effect on ALDH1A1, as evidenced by an IC50 value exceeding 100000.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Cystamine dihydrochloride is a radiation-protective agent. It also protects against carbon tetrachloride liver damage.
靶点活性
Caspase-3:23.6 μM
别名胱胺二盐酸盐
化学信息
分子量225.19
分子式C4H14Cl2N2S2
CAS No.56-17-7
SmilesC(CSSCCN)N.Cl.Cl
密度1.172g/cm3
颜色White
物理性状Solid
储存&溶解度
存储keep away from moisture | 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: 50 mg/mL (222.03 mM), Sonication is recommended.
H2O: 50 mg/mL (222.03 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (8.88 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO/H2O
1mg5mg10mg50mg
1 mM4.4407 mL22.2035 mL44.4069 mL222.0347 mL
5 mM0.8881 mL4.4407 mL8.8814 mL44.4069 mL
10 mM0.4441 mL2.2203 mL4.4407 mL22.2035 mL
20 mM0.2220 mL1.1102 mL2.2203 mL11.1017 mL
50 mM0.0888 mL0.4441 mL0.8881 mL4.4407 mL
100 mM0.0444 mL0.2220 mL0.4441 mL2.2203 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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