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Mecamylamine hydrochloride

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纯度: 99.76%

货号 T2141Cas号 826-39-1

别名 盐酸美加明, Mevasin, Inversine

Mecamylamine hydrochloride (Mevasin) 是一种易穿过血脑屏障的烟碱拮抗剂,用作高血压的神经节阻滞剂,具有抗神经疾病作用。

Mecamylamine hydrochloride
其他形式的 “Mecamylamine hydrochloride”:

Mecamylamine hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.76%

货号 T2141 别名 盐酸美加明, Mevasin, InversineCas号 826-39-1

Mecamylamine hydrochloride (Mevasin) 是一种易穿过血脑屏障的烟碱拮抗剂,用作高血压的神经节阻滞剂,具有抗神经疾病作用。

规格价格库存数量
1 mg
¥ 228
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5 mg
¥ 578
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10 mg
¥ 955
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25 mg
¥ 1,920
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50 mg
¥ 2,720
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100 mg
¥ 3,990
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200 mg
¥ 5,680
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1 mL x 10 mM (in DMSO)
¥ 638
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产品介绍


Mecamylamine hydrochloride AI Summary
Mecamylamine hydrochloride exhibits a range of bioactivities across various biological targets and cell lines. It shows antiplasmodial activity against Plasmodium falciparum GB4 and W2 strains with IC50 values of 12,589.25 nM and 6,309.57 nM, respectively, as measured by SYBR green assays over 72 hours. Additionally, it functions as an inhibitor of Polymerase Iota with a potency of 15.8 nM and impacts the binding or entry of Marburg Virus with potencies ranging from 1,834.9 nM to 22,387.2 nM. In transfected CHO cells, Mecamylamine hydrochloride significantly inhibits sodium fluorescein uptake in OATP1B1- and OATP1B3-transfected cells at a concentration of 10 µM, demonstrating 93.56% and 106.78% inhibition, respectively. The compound also affects cell viability in Vero E6 cells infected with SARS-CoV-2, showing an inhibition index of 0.674 compared to the arbidol control after 72 hours. When tested on HEK293T and U2OS cell lines, Mecamylamine hydrochloride exhibits variable growth rates, ranging from 0.74 to 0.95 and -0.76 to 1.0, respectively. Likewise, in human fibroblast cells, the growth rates range from -1.0 to 0.92, indicating both stimulatory and inhibitory effects on cell viability. Overall, Mecamylamine hydrochloride demonstrates a diverse bioactivity profile, impacting multiple targets and cellular processes..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Mecamylamine hydrochloride (Mevasin) is a nicotinic antagonist, used as a ganglionic blocker in hypertension.
别名盐酸美加明, Mevasin, Inversine
化学信息
分子量203.75
分子式C11H22ClN
CAS No.826-39-1
SmilesCl.N(C)C1(C)C2CCC(C2)C1(C)C
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: 35.71 mg/mL (175.26 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (9.82 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 mM4.9080 mL24.5399 mL49.0798 mL245.3988 mL
5 mM0.9816 mL4.9080 mL9.8160 mL49.0798 mL
10 mM0.4908 mL2.4540 mL4.9080 mL24.5399 mL
20 mM0.2454 mL1.2270 mL2.4540 mL12.2699 mL
50 mM0.0982 mL0.4908 mL0.9816 mL4.9080 mL
100 mM0.0491 mL0.2454 mL0.4908 mL2.4540 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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