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美托咪定 /Medetomidine {[allProObj[0].p_purity_real_show]}

货号:A102119

Medetomidine is an agonist of α2-adrenoceptor with Ki value of 1.08 nM, used as both a surgical anesthetic and analgesic.

Medetomidine 化学结构 CAS号:86347-14-0
Medetomidine 化学结构
CAS号:86347-14-0
Medetomidine 3D分子结构
CAS号:86347-14-0
Medetomidine 化学结构 CAS号:86347-14-0
Medetomidine 3D分子结构 CAS号:86347-14-0
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Medetomidine 纯度/质量文件 产品仅供科研

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产品名称 Adrenergic Receptor α-adrenergic receptor β-adrenergic receptor 其他靶点 纯度
Ivabradine HCl 98%
Maprotiline hydrochloride 98%
Cisatracurium besylate 98%
Yohimbine HCI 99+%
BMY 7378 ++

α2C-adrenoceptor, pKi: 6.54

α1D-adrenoceptor, pKi: 5.1

+

β1-adrenoceptor, pIC50: 5.1

97%
Asenapine maleate ++++

α2B-adrenergic receptor, pKi: 8.9

α2A-adrenergic receptor, pKi: 8.9

97%
Piribedil ++

adrenoceptor α2A, pKi: 7.1

adrenoceptor α2C, pKi: 7.2

98%
Prazosin HCl 95%
Silodosin 98%
Phenoxybenzamine HCl 98%
Naftopidil +++

α1D-adrenergic receptor, Ki: 20 nM

α1A-adrenergic receptor, Ki: 3.7 nM

98%
Naftopidil 2HCl +

α1-adrenergic receptor, IC50: 0.2 μM

97%
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Terazosin HCl 99%
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Tolazoline HCl 98%
Zenidolol hydrochloride ++++

β1-adrenergic receptor, Ki: 611nM

β2-adrenergic receptor, Ki: 0.7nM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Medetomidine 生物活性

描述 Medetomidine is an alpha2-adrenergic receptor agonist and is used clinically in veterinary medicine to produce sedation and analgesia, with Ki values of 1.08 and 1750 nM for α2- and α1-adrenoceptors, respectively. Due to its lipophilic structure, medetomidine is rapidly absorbed after intramuscular administration and reaches peak plasma concentrations in approximately 0.5h[3]. In vivo research suggests that medetomidine has many beneficial effects in anesthesia practice, including reliable sedation, analgesia, muscle relaxation, and anxiolysis[4].

Medetomidine 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT01524367 Agitation Phase 4 Completed - Korea, Republic of ... 展开 >> Gangnam severance hospital Seoul, Korea, Republic of 收起 <<

Medetomidine 参考文献

[1]Wenger S, Hoby S, et al. Anaesthesia with medetomidine, midazolam and ketamine in six gorillas after premedication with oral zuclopenthixol dihydrochloride. Vet Anaesth Analg. 2013 Mar;40(2):176-80.

[2]Kallio A, Koulu M, et al. Acute effects of medetomidine, a selective alpha 2-adrenoceptor agonist, on anterior pituitary hormone and cortisol secretion in man. Acta Endocrinol (Copenh). 1988 Sep;119(1):11-5.

[3]Lamont LA, Burton SA, Caines D, Troncy ED. Effects of 2 different infusion rates of medetomidine on sedation score, cardiopulmonary parameters, and serum levels of medetomidine in healthy dogs. Can J Vet Res. 2012 Oct;76(4):308-16. PMID: 23543957; PMCID: PMC3460610.

[4]Pawela CP, Biswal BB, Hudetz AG, Schulte ML, Li R, Jones SR, Cho YR, Matloub HS, Hyde JS. A protocol for use of medetomidine anesthesia in rats for extended studies using task-induced BOLD contrast and resting-state functional connectivity. Neuroimage. 2009 Jul 15;46(4):1137-47. doi: 10.1016/j.neuroimage.2009.03.004. Epub 2009 Mar 12. PMID: 19285560; PMCID: PMC2693293.

Medetomidine 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.99mL

1.00mL

0.50mL

24.97mL

4.99mL

2.50mL

49.93mL

9.99mL

4.99mL

Medetomidine 技术信息

CAS号86347-14-0
分子式C13H16N2
分子量 200.28
别名
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Sealed in dry,Room Temperature

溶解度

DMSO: 250 mg/mL(1248.26 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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