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Amifampridine

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纯度: 99.82%

货号 T4497Cas号 54-96-6

别名 阿米吡啶, Pyridine-3,4-Diamine, 3,4-Pyridinediamine, 3,4-Diaminopyridine

Amifampridine (3,4-Diaminopyridine) 可用于罕见肌肉疾病的研究。

Amifampridine
其他形式的 “Amifampridine”:

Amifampridine

一键复制产品信息
Rating icon 很棒

纯度: 99.82%

货号 T4497 别名 阿米吡啶, Pyridine-3,4-Diamine, 3,4-Pyridinediamine, 3,4-DiaminopyridineCas号 54-96-6

Amifampridine (3,4-Diaminopyridine) 可用于罕见肌肉疾病的研究。

规格价格库存数量
1 g
¥ 99
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1 mL x 10 mM (in DMSO)
¥ 99
现货
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产品介绍


Amifampridine AI Summary
Amifampridine exhibits a diverse range of bioactivities. Primarily, the compound selectively increases both basal and K+-stimulated acetylcholine (AcCh) release across various brain regions, including the hippocampus, cortex, and striatum, with dose-dependent effects in these areas. Additionally, it inhibits [3H]choline uptake at choline transporter 1 in mouse brain synaptosomes with a Ki value of 820351.54 nM. Beyond its impact on neurotransmitter release, Amifampridine demonstrates inhibitory activities against multiple targets such as lipid storage, AmpC beta-lactamase, histone lysine methyltransferase G9a, and several others, with potencies in the nanomolar to micromolar range. The compound also shows antiviral properties, including inhibition of cytotoxicity induced by SARS-CoV-2 in various cell lines and inhibition of the SARS-CoV-2 3CL-Pro protease. However, its effectiveness against SARS-CoV-2 is limited, with an IC50 value greater than 20000.0 nM and variable inhibition percentages. Additionally, the compound exhibits notable activity in an enzymatic assay of human HDAC6 and functions as a substrate for human OCT1, characterized by specific kinetic parameters and intrinsic clearance values. Despite these activities, Amifampridine has shown no significant bioactivity in binding affinity and inhibition assays against several human and rat receptors, enzymes, and ion channels, with all AC50 values exceeding 30,000.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Amifampridine (3,4-Diaminopyridine) is predominantly in the treatment of a number of rare muscle diseases. Amifampridine works by blocking potassium channel efflux in nerve terminals so that action potential duration is increased. Ca2+ channels can then be open for a longer time and allow greater acetylcholine release to stimulate muscle at the end plate.
别名阿米吡啶, Pyridine-3,4-Diamine, 3,4-Pyridinediamine, 3,4-Diaminopyridine
化学信息
分子量109.13
分子式C5H7N3
CAS No.54-96-6
SmilesNC1=C(N)C=NC=C1
密度1.251g/cm3
颜色Red
物理性状Solid
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
H2O: 24 mg/mL (219.92 mM), Sonication is recommended.
DMSO: 60 mg/mL (549.8 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (18.33 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
H2O/DMSO
1mg5mg10mg50mg
1 mM9.1634 mL45.8169 mL91.6338 mL458.1692 mL
5 mM1.8327 mL9.1634 mL18.3268 mL91.6338 mL
10 mM0.9163 mL4.5817 mL9.1634 mL45.8169 mL
20 mM0.4582 mL2.2908 mL4.5817 mL22.9085 mL
50 mM0.1833 mL0.9163 mL1.8327 mL9.1634 mL
100 mM0.0916 mL0.4582 mL0.9163 mL4.5817 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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