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Amitraz

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纯度: 99.88%

货号 T1632Cas号 33089-61-1

别名 双甲脒, NSC 324552, BTS-27419

Amitraz (NSC 324552) 是一种非系统性杀螨剂和杀虫剂,,可治疗犬蠕形螨。它具有α-肾上腺素能激动剂活性, 与中枢神经系统的章鱼胺受体相互作用, 抑制单胺氧化酶和前列腺素合成。

Amitraz

Amitraz

一键复制产品信息
Rating icon 很棒

纯度: 99.88%

货号 T1632 别名 双甲脒, NSC 324552, BTS-27419Cas号 33089-61-1

Amitraz (NSC 324552) 是一种非系统性杀螨剂和杀虫剂,,可治疗犬蠕形螨。它具有α-肾上腺素能激动剂活性, 与中枢神经系统的章鱼胺受体相互作用, 抑制单胺氧化酶和前列腺素合成。

规格价格库存数量
200 mg
¥ 147
现货
500 mg
¥ 248
现货
1 g
¥ 357
现货
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产品介绍


Amitraz AI Summary
Amitraz exhibits a wide range of bioactivities across various biological targets and systems. It shows high potency in modulating Lamin A splicing with an EC50 of 0.9 nM, while demonstrating significantly lower potency in other assays such as activating Cytochrome P450 3A4 (39810.7 nM) and thyroid hormone receptor beta (44668.4 nM). The compound functions as both an agonist and antagonist of peroxisome proliferator-activated receptor gamma (PPARγ) with potencies of 39810.7 nM and 50118.7 nM, respectively, and similarly activates Aryl hydrocarbon Receptor (50118.7 nM) and the antioxidant response element (ARE) signaling pathway (24336.5 nM). It induces DNA re-replication in SW480 colon adenocarcinoma cells with a potency of 33498.3 nM and exhibits modest inhibition of Human Apurinic/apyrimidinic Endonuclease 1 (APE1) at 31622.8 nM. In virological assays, it inhibits Ebola virus entry (25118.9 to 631.0 nM) and SARS-CoV-2 induced cytotoxicity in Caco-2 and VERO-6 cells. In addition to its antiviral capabilities, Amitraz demonstrates antitrypanosomal activity against Trypanosoma cruzi with an EC50 of 16000.0 nM and exhibits cytotoxicity against BESM cells with an EC50 of 33000.0 nM. It acts as a ligand for Alpha-2A adrenergic receptor and Imidazoline I2, Central receptors, showing IC50 values between 47.7 and 926.9 nM. The compound also demonstrates significant insecticidal activity against two-spotted spider mite Tetranychus urticae and shows toxicity to worker Bombus terrestris (bumblebees). Pharmacokinetically, Amitraz influences multiple physiological systems, including liver and kidney function, electrolyte balance, cholesterol metabolism, and various hematological parameters based on DrugMatrix assay results. Furthermore, it inhibits human HDAC6 enzyme activity, suggesting potential bioactivity in modulating epigenetic functions. Overall, Amitraz is a multifunctional molecule with broad-spectrum bioactivities, significant antiviral potential, insecticidal properties, and the ability to modulate multiple physiological and enzymatic pathways..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Amitraz (NSC 324552) is a white monoclinic crystals. Melting point 187-189°F (86-87°C). Insoluble in water. Used as an acaricide, insecticide and treatment of demodectic mange in dogs.
别名双甲脒, NSC 324552, BTS-27419
化学信息
分子量293.41
分子式C19H23N3
CAS No.33089-61-1
SmilesN(=CN(C=NC1=C(C)C=C(C)C=C1)C)C2=C(C)C=C(C)C=C2
密度1.1280 g/cm3
储存&溶解度
存储store at low temperature | 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: 50 mg/mL (170.41 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.82 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 mM3.4082 mL17.0410 mL34.0820 mL170.4100 mL
5 mM0.6816 mL3.4082 mL6.8164 mL34.0820 mL
10 mM0.3408 mL1.7041 mL3.4082 mL17.0410 mL
20 mM0.1704 mL0.8521 mL1.7041 mL8.5205 mL
50 mM0.0682 mL0.3408 mL0.6816 mL3.4082 mL
100 mM0.0341 mL0.1704 mL0.3408 mL1.7041 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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