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A9611

Sigma-Aldrich

Atipamezole

≥98% (HPLC)

Sinónimos:

4-(2-Ethyl-2,3-dihydro-1H-inden-2-yl)-1H-Imidazole, Antisedan, MPV 1248

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5 MG
$124.00
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$451.25

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5 MG
$124.00
25 MG
$451.25

About This Item

Fórmula empírica (notación de Hill):
C14H16N2
Número de CAS:
104054-27-5
Peso molecular:
212.29
Número MDL:
MFCD00864502
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
329771055
NACRES:
NA.77

$124.00

Disponible para envío el08 de abril de 2025Detalles

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Ensayo

≥98% (HPLC)

Formulario

powder

color

white to brown

solubilidad

DMSO: ≥30 mg/mL

temp. de almacenamiento

room temp

cadena SMILES

CCC1(Cc2ccccc2C1)c3c[nH]cn3

InChI

1S/C14H16N2/c1-2-14(13-9-15-10-16-13)7-11-5-3-4-6-12(11)8-14/h3-6,9-10H,2,7-8H2,1H3,(H,15,16)

Clave InChI

HSWPZIDYAHLZDD-UHFFFAOYSA-N

Descripción general

Atipamezole has an imidazole structure and gets localized in the central nervous system on administration.[1]

Aplicación

Atipamezole has been used as a α2-adrenoceptor antagonist in mesencephalic trigeminal nucleus (MTN) neurons,[2] CD4+ T-lymphocyte[3] and human embryonic kidney (HEK293) membrane preparation.[4]

Acciones bioquímicas o fisiológicas

Atipamezole elicits affinity towards adrenoreceptor subtypes namely α2A, α2B and α2C. High levels of atipamezole impairs cognitive functions. It also reverses the adrenoreceptor agonist functionalities.[1] Atipamezole shows no affinity towards muscarinic[1] and dopamine or neurotransmitter receptors.[5] Atipamezole when used along with morphine elicits antinociceptive effects.[6]
Atipamezole is a selective α2 adrenergic blocker. Atipamezole is more potent than yohimbine; it is very selective for α2 adrenergic vs α1 sites, but not selelctive for α2 subtypes.
Atipamezole is a selective α2 adrenergic blocker; neutral antagonist

Características y beneficios

This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the α2-Adrenoceptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number
0000213795
0000064006
0000141686
0000141687
0000139669

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Brian Milne et al.
Anesthesia and analgesia, 112(6), 1500-1503 (2011-05-06)
Ultralow-dose opioid antagonists prolong opioid antinociception and block tolerance. In this study we determined whether low doses of the α-2 adrenergic receptor (A2-R) antagonist, atipamezole, similarly influenced A2-R-induced antinociception and tolerance. In rats, intrathecal norepinephrine (NE) or clonidine in combination
A Olsson et al.
Australian veterinary journal, 90(6), 240-244 (2012-05-29)
Restraint of large estuarine crocodiles is potentially dangerous. Neuromuscular blockers and other immobilising drugs have been used with variable results. Medetomidine has been reported as a reliable, repeatable and reversible immobilisation agent in small estuarine crocodilians. Two wild and two
Antti Pertovaara et al.
CNS drug reviews, 11(3), 273-288 (2006-01-04)
Atipamezole is an alpha2-adrenoceptor antagonist with an imidazole structure. Receptor binding studies indicate that its affinity for alpha2-adrenoceptors and its alpha2/alpha1 selectivity ratio are considerably higher than those of yohimbine, the prototype alpha2-adrenoceptor antagonist. Atipamezole is not selective for subtypes
Annabelle Olsson et al.
Veterinary anaesthesia and analgesia, 39(4), 345-356 (2012-05-31)
To establish a safe, reliable and reversible immobilization protocol for captive juvenile crocodiles. Prospective, randomized, clinical study. Thirty male estuarine crocodiles (body mass 1-12.1 kg) and 10 male Australian freshwater crocodiles (body mass 4.1-12.8 kg). An optimized dose of medetomidine
The C-terminal half of the alpha 2C-adrenoceptor determines the receptor's membrane expression level and drug selectivity
Jahnsen JA and Uhlen S
Naunyn-Schmiedeberg'S Archives of Pharmacology, 386(12), 1031-1040 (2013)
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