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Proadifen hydrochloride

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Rating icon 很棒

纯度: 99.98%

货号 T1597Cas号 62-68-0

别名 盐酸丙基解痉素, U-5446, SKF-525A, RP-5171

Proadifen hydrochloride (RP-5171) 是细胞色素 P450抑制剂,它的 IC50值为19μM。

Proadifen hydrochloride
其他形式的 “Proadifen hydrochloride”:

Proadifen hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.98%

货号 T1597 别名 盐酸丙基解痉素, U-5446, SKF-525A, RP-5171Cas号 62-68-0

Proadifen hydrochloride (RP-5171) 是细胞色素 P450抑制剂,它的 IC50值为19μM。

规格价格库存数量
50 mg
¥ 142
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100 mg
¥ 255
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1 mL x 10 mM (in DMSO)
¥ 150
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产品介绍


Proadifen hydrochloride AI Summary
Proadifen hydrochloride exhibits a broad spectrum of bioactivities. It demonstrates potent antispasmodic activity against isolated guinea pig ileum, with an IC50 value of 0.0000012 M, and a potency relative to adiphenine of 0.62. It inhibits several enzymatic activities, such as Aryl hydrocarbon hydroxylase and Aminopyrine N-demethylase, with IC50 values of 22000.0 nM and 8200.0 nM respectively in phenobarbitone-treated rats. Additionally, it shows antiplasmodial activity against various strains of Plasmodium falciparum with IC50 values ranging from 1584.89 nM to 7943.28 nM. The compound inhibits sodium fluorescein uptake in OATP1B1 and OATP1B3 transfected CHO cells. Furthermore, it demonstrates cytotoxicity in a HepG2 cell line with an IC50 of 57000.0 nM, and inhibits mitochondrial permeability transition pore as well as several specific enzymes and proteins, including HSD17B4, JMJD2E, TGF-b, and USP1/UAF1. Additionally, Proadifen hydrochloride activates the human and rat pregnane X receptor (PXR), inducing CYP3A4 expression in human liver cells, and exhibits antiviral activity against SARS-CoV-2 with inhibitory effects on both 3CL-Pro protease and virus-induced cytotoxicity in various cell lines. Its multifunctional bioactivities make it a potential candidate for further pharmacological investigation..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Proadifen hydrochloride (RP-5171) is an inhibitor of drug metabolism and cytochrome P-450 enzyme system activity.
靶点活性
CYP:19μM
别名盐酸丙基解痉素, U-5446, SKF-525A, RP-5171
化学信息
分子量389.96
分子式C23H32ClNO2
CAS No.62-68-0
SmilesCl.CCCC(C(=O)OCCN(CC)CC)(c1ccccc1)c1ccccc1
密度no data available
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: 45 mg/mL (115.4 mM), Sonication is recommended.
H2O: 197.4 mM, Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.13 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 mM2.5644 mL12.8218 mL25.6437 mL128.2183 mL
5 mM0.5129 mL2.5644 mL5.1287 mL25.6437 mL
10 mM0.2564 mL1.2822 mL2.5644 mL12.8218 mL
20 mM0.1282 mL0.6411 mL1.2822 mL6.4109 mL
50 mM0.0513 mL0.2564 mL0.5129 mL2.5644 mL
100 mM0.0256 mL0.1282 mL0.2564 mL1.2822 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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