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Orphenadrine hydrochloride

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纯度: 99.88%

货号 T1308Cas号 341-69-5

别名 盐酸邻甲苯海拉明, Mephenamin, Mebedrol

Orphenadrine hydrochloride (Mephenamin) 是一种非竞争性的NMDA 受体拮抗剂, Ki=6.0 ± 0.7 μM。

Orphenadrine hydrochloride
其他形式的 “Orphenadrine hydrochloride”:

Orphenadrine hydrochloride

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Rating icon 很棒

纯度: 99.88%

货号 T1308 别名 盐酸邻甲苯海拉明, Mephenamin, MebedrolCas号 341-69-5

Orphenadrine hydrochloride (Mephenamin) 是一种非竞争性的NMDA 受体拮抗剂, Ki=6.0 ± 0.7 μM。

规格价格库存数量
5 mg
¥ 279
现货
10 mg
¥ 393
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25 mg
¥ 659
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50 mg
¥ 978
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100 mg
¥ 1,450
现货
200 mg
¥ 2,150
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500 mg
¥ 3,630
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1 g
¥ 5,250
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1 mL x 10 mM (in DMSO)
¥ 323
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产品介绍


Orphenadrine hydrochloride AI Summary
Orphenadrine hydrochloride exhibits a range of bioactivities, demonstrating antiplasmodial activity against various Plasmodium falciparum strains, with IC50 values ranging from 630.96 nM to 11220.2 nM. It shows efficacy in inhibiting the growth of infected Vero E6 cells with SARS-CoV-2, with an inhibition index of 0.9732. The compound also modulates Lamin A splicing, induces erasure of genomic imprints, and inhibits Bloom's syndrome helicase. Furthermore, it acts as an antagonist of the Neuropeptide S receptor and inhibits several enzymes and receptors, including thyroid hormone receptor beta, Histone Lysine Methyltransferase G9a, Mammalian Selenoprotein Thioredoxin Reductase 1, human hERG channel activity, and human Apurinic/apyrimidinic Endonuclease 1. It induces DNA re-replication in MCF 10a normal breast cells and shows activity against Hepatitis C Virus. Additionally, Orphenadrine hydrochloride exhibits moderate antifungal activity against Candida albicans and varying antibacterial activities, ranging from weak to strong inhibition against multiple bacterial strains, including moderate to strong inhibition against Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Staphylococcus aureus MRSA..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Orphenadrine hydrochloride (Mephenamin) is a muscarinic antagonist used to treat drug-induced parkinsonism and to relieve pain from muscle spasm.
靶点活性
NMDAR:6.0 ±0.7 μM (Ki)
别名盐酸邻甲苯海拉明, Mephenamin, Mebedrol
化学信息
分子量305.85
分子式C18H23NO·HCl
CAS No.341-69-5
SmilesCl.CN(C)CCOC(c1ccccc1)c1ccccc1C
密度1.014g/cm3
颜色White
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
DMSO: 45 mg/mL (147.13 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM3.2696 mL16.3479 mL32.6958 mL163.4788 mL
5 mM0.6539 mL3.2696 mL6.5392 mL32.6958 mL
10 mM0.3270 mL1.6348 mL3.2696 mL16.3479 mL
20 mM0.1635 mL0.8174 mL1.6348 mL8.1739 mL
50 mM0.0654 mL0.3270 mL0.6539 mL3.2696 mL
100 mM0.0327 mL0.1635 mL0.3270 mL1.6348 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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