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Clopamide

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纯度: 99.71%

货号 T6086Cas号 636-54-4

别名 氯帕胺, Brinaldix, Aquex, Adurix

Clopamide (Brinaldix) 是口服有效的噻嗪类利尿剂,对钠耦合的氯离子共转运蛋白 SLC12A3有抑制作用。Clopamide 在高血压和心力衰竭中具有研究价值。

Clopamide
其他形式的 “Clopamide”:

Clopamide

一键复制产品信息
Rating icon 很棒

纯度: 99.71%

货号 T6086 别名 氯帕胺, Brinaldix, Aquex, AdurixCas号 636-54-4

Clopamide (Brinaldix) 是口服有效的噻嗪类利尿剂,对钠耦合的氯离子共转运蛋白 SLC12A3有抑制作用。Clopamide 在高血压和心力衰竭中具有研究价值。

规格价格库存数量
25 mg
¥ 296
4-6周
50 mg
¥ 417
4-6周
100 mg
¥ 671
4-6周
1 mL x 10 mM (in DMSO)
¥ 195
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产品介绍


Clopamide AI Summary
Clopamide exhibits a range of bioactivities with varying potencies across multiple targets. It shows moderate potency (316.2 nM) in altering Lamin A splicing and a higher potency as an inhibitor of HSD17B4 (19952.6 nM). The compound also exhibits moderate potencies in inducing genomic imprint erasure (5011.9 nM), inhibiting chronic active B-cell receptor signaling (5804.8 nM), and inhibiting cell surface uPA generation (8912.5 nM). It demonstrates good potency (585.8 nM) as a delayed death inhibitor of the malarial parasite plastid after 96 hours of incubation and notable potency (1000.0 nM) in inducing DNA re-replication in SW480 colon adenocarcinoma cells. Additionally, it shows moderate potency (6309.6 nM) as an inhibitor of TDP-43. The compound displays low bioactivity in inhibiting the cell viability of Vero E6 cells infected with SARS-CoV-2, with an inhibition index of 0.2254, suggesting limited effectiveness compared to the control. It exhibits weak antiviral activity against SARS-CoV-2 in VERO-6 cells with an IC50 value greater than 20000.0 nM. In terms of HDAC6 inhibition, the compound shows a 10.39% inhibition rate using a commercial peptide substrate but -4.01% using a custom peptide substrate. Further assessments indicate that Clopamide demonstrated no significant bioactivity in various assays, showing AC50 values greater than 30000.0 nM across different targets such as ion channels, neurotransmitter receptors, enzymes, and nuclear receptors, and it did not exhibit significant agonist or antagonist effects in the tested in vitro assays..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Clopamide (Brinaldix) is a piperidine and sulfamoylbenzamide-based diuretic with thiazide-like diuretic activity.
别名氯帕胺, Brinaldix, Aquex, Adurix
化学信息
分子量345.84
分子式C14H20ClN3O3S
CAS No.636-54-4
SmilesCC1CCCC(C)N1NC(=O)c1ccc(Cl)c(c1)S(N)(=O)=O
密度1.39 g/cm3
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: 25 mg/mL (72.29 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.78 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
1mg5mg10mg50mg
1 mM2.8915 mL14.4576 mL28.9151 mL144.5755 mL
5 mM0.5783 mL2.8915 mL5.7830 mL28.9151 mL
10 mM0.2892 mL1.4458 mL2.8915 mL14.4576 mL
20 mM0.1446 mL0.7229 mL1.4458 mL7.2288 mL
50 mM0.0578 mL0.2892 mL0.5783 mL2.8915 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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