Dexmedetomidine hydrochloride

Pricing Availability   Qty
Description: Potent, highly selective α2 agonist. Active isomer of medetomidine (Cat. No. 5160)
Alternative Names: d-Medetomidine hydrochloride
Chemical Name: 4-[(1S)-1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole hydrochloride
Purity: ≥98%
Datasheet
Citations (7)
Reviews
Literature (2)

Biological Activity for Dexmedetomidine hydrochloride

Dexmedetomidine hydrochloride is an active isomer of medetomidine, a potent, highly selective α2-adrenoceptor agonist (Ki values are 1.08 and 1750 nM for α2- and α1-adrenoceptors respectively). Displays greater selectivity over α1-adrenoceptors than Clonidine (Cat. No. 0690) and UK 14,304 (1620-, 220- and 300-fold respectively). Active in vivo; displays hypotensive, bradycardic, sedative, anxiolytic, hypothermic and analgesic effects.

Racemate also available.

Compound Libraries for Dexmedetomidine hydrochloride

Dexmedetomidine hydrochloride is also offered as part of the Tocriscreen FDA-Approved Drugs. Find out more about compound libraries available from Tocris.

Technical Data for Dexmedetomidine hydrochloride

M. Wt 236.74
Formula C13H16N2.HCl
Storage Desiccate at RT
Purity ≥98%
CAS Number 145108-58-3
PubChem ID 6918081
InChI Key VPNGEIHDPSLNMU-MERQFXBCSA-N
Smiles C[C@H](C2=CN=CN2)C1=C(C)C(C)=CC=C1.Cl

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

Tocris products are intended for laboratory research use only, unless stated otherwise.

Solubility Data for Dexmedetomidine hydrochloride

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
water 23.67 100
DMSO 23.67 100

Preparing Stock Solutions for Dexmedetomidine hydrochloride

The following data is based on the product molecular weight 236.74. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 4.22 mL 21.12 mL 42.24 mL
5 mM 0.84 mL 4.22 mL 8.45 mL
10 mM 0.42 mL 2.11 mL 4.22 mL
50 mM 0.08 mL 0.42 mL 0.84 mL

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Product Datasheets for Dexmedetomidine hydrochloride

Certificate of Analysis / Product Datasheet
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References for Dexmedetomidine hydrochloride

References are publications that support the biological activity of the product.

Virtanen et al (1988) Characterization of the selectivity, specificity and potency of medetomidine as an α2-adrenoceptor agonist. Eur.J.Pharmacol. 150 9 PMID: 2900154

Fisher et al (1991) Antinociceptive properties of intrathecal dexmedetom. in rats. Eur.J.Pharmacol. 192 221 PMID: 1674472

Scheinin et al (1989) Medetomidine - a novel α2-adrenoceptor agonist: a review of its pharmacodynamic effects. Prog.Neuro-Psychopharm.Biol.Psychiat. 13 635 PMID: 2571177


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7 Citations for Dexmedetomidine hydrochloride

Citations are publications that use Tocris products. Selected citations for Dexmedetomidine hydrochloride include:

Yuki et al (2011) Sedative drug modulates T-cell and lymphocyte function-associated antigen-1 function. Anesth Analg 112 830 PMID: 21385989

Uchida et al (2019) Induction of Non-Apoptotic Cell Death by Adrenergic Agonists in Human Oral Squamous Cell Carcinoma Cell Lines. Anticancer Res 39 3519 PMID: 31262876

Rennekamp et al (2016) σ1 receptor ligands control a switch between passive and active threat responses. Nat Chem Biol 12 552 PMID: 27239788

Gozzi et al (2013) Differential effect of orexin-1 and CRF-1 antagonism on stress circuits: a fMRI study in the rat with the pharmacological stressor Yohimbine. Neuropsychopharmacology 38 2120 PMID: 23736277

Ma et al (2019) Galanin Neurons Unite Sleep Homeostasis and α2-Adrenergic Sedation Curr Biol 29 3315 PMID: 31543455

Garrity et al (2015) Dexmedetomidine-induced sedation does not mimic the neurobehavioral phenotypes of sleep in Sprague Dawley rat. Invest Ophthalmol Vis Sci 38 73 PMID: 25325438

McAlvin et al (2015) Corneal Anesthesia With Site 1 Sodium Channel Blockers and dexmedetom. J Inflamm (Lond) 56 3820 PMID: 26066750


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Literature in this Area

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

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