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Merck
CN

SML0956

Sigma-Aldrich

右美托咪啶 盐酸盐

≥98% (HPLC)

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别名:
(+)-美托咪定 盐酸盐, (S)-美托咪定 盐酸盐, 4-[(S)-α2,3-三甲基苄基咪唑 单盐酸盐, 5-[(1S)-1-(2,3-二甲基苯基)乙基]-1H-咪唑 盐酸盐
经验公式(希尔记法):
C13H16N2 · HCl
分子量:
236.74
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

检测方案

≥98% (HPLC)

形式

powder

旋光性

[α]/D +48 to +58°, c = 1 in H2O

储存条件

desiccated

颜色

white to beige

溶解性

H2O: 20 mg/mL, clear

储存温度

2-8°C

InChI

1S/C13H16N2.ClH/c1-9-5-4-6-12(10(9)2)11(3)13-7-14-8-15-13;/h4-8,11H,1-3H3,(H,14,15);1H/t11-;/m0./s1

InChI key

VPNGEIHDPSLNMU-MERQFXBCSA-N

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应用

盐酸右美托咪定已被用于研究其在缺氧/复氧条件下对原代乳鼠心肌细胞的影响。也用于研究右美托咪定预处理对脂多糖诱导的小鼠急性肺损伤的影响。

生化/生理作用

盐酸右美托咪定是一种高效选择性且具有镇痛和镇静属性的 α2-肾上腺素能激动剂,是美托咪定的 (+)-异构体。盐酸右美托咪定在临床上作为一种麻醉剂,用于减轻焦虑和紧张情绪,促进松弛和镇静,而不引起呼吸抑制。

特点和优势

这种化合物是神经科学研究的特色产品。 点击此处 ,发现更多特色神经科学产品。前往 sigma.com/discover-bsm 了解更多关于其他研究领域的生物活性小分子。

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Aquatic Chronic 2 - STOT SE 3

靶器官

Central nervous system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Dexmedetomidine is an α2-adrenoceptor agonist used for perioperative and intensive care sedation. This study develops mechanism-based population pharmacokinetic-pharmacodynamic models for the cardiovascular and central nervous system (CNS) effects of intravenously (IV) and intranasally (IN) administered dexmedetomidine in healthy subjects. Single
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Journal of biochemical and molecular toxicology, 36(6), e23044-e23044 (2022-05-03)
Inhibition of histone deacetylase (HDAC) may be a useful approach in the treatment of disorders characterized by cognitive dysfunction. Dexmedetomidine (DEX), an α2-adrenoceptor (α2-AR) agonist, has demonstrated neuroprotective effects. Here, we attempted to investigate the protective effects of DEX on
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Dexmedetomidine (DEX), a selective α2 adrenergic receptor (AR) agonist, is commonly used as a sedative drug during critical illness. In the present study, we explored a novel accelerative effect of DEX on cardiac fibroblast (CF) differentiation mediated by LPS and
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To explore the anti-inflammatory effect and the potential mechanism of dexmedetomidine in ARDS/ALI. C57BL/6 mice and EL-4 cells were used in this research. The ALI model was established by CLP. The level of inflammatory cytokines in the lung and blood

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