Dexmedetomidine
Dexmedetomidine ((+) -Medetomidine) is a potent, selective and orally active agonist of α2-adrenoceptor, with a Ki of 1.08 nM. Dexmedetomidine shows 1620-fold selectivity against α1-adrenoceptor. Dexmedetomidine exhibits anxiolysis, sedation, and modest analgesia effects[1][2][3].
Product Specifications
CAS Number
[113775-47-6]
Product Name Alternative
(+) -Medetomidine; (S) -Medetomidine
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
Adrenergic Receptor
Type
Reference compound
Related Pathways
GPCR/G Protein; Neuronal Signaling
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease; Cancer
Assay Protocol
https://www.medchemexpress.com/dexmedetomidine.html
Purity
99.93
Solubility
DMSO : 125 mg/mL (ultrasonic)
Smiles
C[C@H](C1=CN=CN1)C2=CC=CC(C)=C2C
Molecular Formula
C13H16N2
Molecular Weight
200.28
Precautions
H302, H315, H319, H335
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, protect from light)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
α adrenergic receptor
Citation 01
Available Sizes
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