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I6138

Idazoxan hydrochloride

α2-adrenoceptor antagonist

Synonym(s):

(±)-2-[1,4-Benzodioxan-2-yl]-2-imidazoline hydrochloride, RX 781094

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50 mg
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CLP 95,400
100 mg
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CLP 126,000

About This Item

Empirical Formula (Hill Notation):
C11H12N2O2 · HCl
CAS Number:
79944-56-2
Molecular Weight:
240.69
UNSPSC Code:
12352200
PubChem Substance ID:
24278493
NACRES:
NA.77
MDL number:
MFCD00069293
Quality level:
100

CLP 95,400

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Product Name

Idazoxan hydrochloride,

Quality Level

100

solubility

H2O: 50 mg/mL

SMILES string

Cl.C1CN=C(N1)C2COc3ccccc3O2

InChI

1S/C11H12N2O2.ClH/c1-2-4-9-8(3-1)14-7-10(15-9)11-12-5-6-13-11;/h1-4,10H,5-7H2,(H,12,13);1H

InChI key

MYUBYOVCLMEAOH-UHFFFAOYSA-N

Gene Information

human ... ADRA2A(150), ADRA2B(151), ADRA2C(152)

Application

Idazoxan hydrochloride has been used to study the efficacy of antidepressant treatments that interact with multiple neurotransmitter systems.

Biochem/physiol Actions

α2-adrenoceptor antagonist; I2 imidazoline receptor agonist; I1 imidazoline receptor antagonist. Idazoxan can antagonize various behaviors generated by ethanol in a preclinical setting. It possesses neuroprotective activity against spinal cord injury, resulted due to experimental autoimmune encephalomyelitis (EAE) in mouse, an animal modal of multiple sclerosis (MS).[1]

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Idazoxan hydrochloride

Sigma-Aldrich

I6138

Idazoxan hydrochloride

RX 821002 hydrochloride solid, ≥98% (HPLC)

Sigma-Aldrich

R9525

RX 821002 hydrochloride

p-Aminoclonidine hydrochloride solid

Sigma-Aldrich

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p-Aminoclonidine hydrochloride

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Sigma-Aldrich

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Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

solubility

H2O: 50 mg/mL

solubility

H2O: >20 mg/mL

solubility

45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 1.4 mg/mL (Solutions may be stored for several days at 4 °C), boiling water: 100 mg/mL (Solutions may be stored for several days at 4 °C), 0.1 M HCl: soluble (Solutions may be stored for several days at 4 °C), methanol: soluble (Solutions may be stored for several days at 4 °C)

solubility

H2O: soluble, methanol: soluble

Gene Information

human ... ADRA2A(150), ADRA2B(151), ADRA2C(152)

Gene Information

human ... ADRA2A(150), ADRA2B(151), ADRA2C(152)

Gene Information

human ... ADRA2A(150), ADRA2B(151), ADRA2C(152)

Gene Information

human ... ADRA2A(150), ADRA2B(151), ADRA2C(152)

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV6984
MKCW0789
MKCW4070
MKCW5110
MKCV4484

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Related Content

Product Information Sheet - I6138

Product Information Sheet

Vidya Narayanaswami et al.
Molecular imaging, 17, 1536012118792317-1536012118792317 (2018-09-12)
The dynamic and multicellular processes of neuroinflammation are mediated by the nonneuronal cells of the central nervous system, which include astrocytes and the brain's resident macrophages, microglia. Although initiation of an inflammatory response may be beneficial in response to injury
Idazoxan and 8-OH-DPAT modify the behavioral effects induced by either NA, or 5-HT, or dual NA/5-HT reuptake inhibition in the rat forced swimming test
Reneric, J P, et al.
Neuropsychopharmacology, 24(4), 379-379 (2001)
Sidney P Kuo et al.
Neuron, 71(2), 306-318 (2011-07-28)
Inhibitory interneurons across diverse brain regions commonly exhibit spontaneous spiking activity, even in the absence of external stimuli. It is not well understood how stimulus-evoked inhibition can be distinguished from background inhibition arising from spontaneous firing. We found that noradrenaline
View All Related Papers

Global Trade Item Number

SKUGTIN
I6138-50MG04061832091525
I6138-100MG04061832091518

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