Dexmedetomidine (hydrochloride)
Dexmedetomidine hydrochloride ((+) -Medetomidine hydrochloride) is a potent, selective and orally active agonist of α2-adrenoceptor, with a Ki of 1.08 nM. Dexmedetomidine hydrochloride shows 1620-fold selectivity against α1-adrenoceptor. Dexmedetomidine hydrochloride exhibits anxiolysis, sedation, and modest analgesia effects[1][2][3].
Product Specifications
CAS Number
[145108-58-3]
Product Name Alternative
(+) -Medetomidine (hydrochloride) ; (S) -Medetomidine (hydrochloride)
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
Adrenergic Receptor
Type
Reference compound
Related Pathways
GPCR/G Protein; Neuronal Signaling
Applications
Cancer-programmed cell death
Field of Research
Cancer; Infection
Assay Protocol
https://www.medchemexpress.com/Dexmedetomidine-hydrochloride.html
Concentration
10mM
Purity
99.94
Solubility
DMSO : 250 mg/mL (ultrasonic) |H2O : ≥ 50 mg/mL
Smiles
C[C@H](C1=CN=CN1)C2=CC=CC(C)=C2C.Cl
Molecular Formula
C13H17ClN2
Molecular Weight
236.74
Precautions
H302, H315, H319, H335
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
α adrenergic receptor
Citation 01
Available Sizes
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