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质量水平
方案
≥98% (HPLC)
表单
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
SMILES字符串
[Cl-].[N+H2]1C=NC=C1[C@@H](C)c2c(c(ccc2)C)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。
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
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
Jia Liao et al.
International journal of molecular sciences, 22(23) (2021-12-11)
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
Yu-Fang Liu et al.
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
Anna K Shoveller et al.
Journal of feline medicine and surgery, 16(12), 957-965 (2014-03-15)
Body condition scoring (BCS) provides a readily available technique that can be used by both veterinary professionals and owners to assess the body condition of cats, and diagnose overweight or underweight conditions. The objective of this study was to evaluate
Heedoo Yoo et al.
European journal of clinical pharmacology, 71(10), 1197-1207 (2015-08-04)
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
Dexmedetomidine attenuates hypoxia/reoxygenation injury in primary neonatal rat cardiomyocytes
Ke Peng
Experimental and Therapeutic Medicine (2017)
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