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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6N2O2.ClH
Molecular Weight 162.574
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IMIDAZOLEACETIC ACID HYDROCHLORIDE

SMILES

Cl.OC(=O)CC1=CNC=N1

InChI

InChIKey=MWHLCFYPFGFBQO-UHFFFAOYSA-N
InChI=1S/C5H6N2O2.ClH/c8-5(9)1-4-2-6-3-7-4;/h2-3H,1H2,(H,6,7)(H,8,9);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C5H6N2O2
Molecular Weight 126.1133
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Quantitative determination of 1,4-methyl-imidazoleacetic acid in urine by high performance liquid chromatography.
1982 Nov
Presence and measurement of methylimidazoleacetic acids in brain and body fluids.
1982 Nov 10
Simultaneous determination of imidazoleacetic acid and N tau- and N pi-methylimidazoleacetic acids in human urine by high-performance liquid chromatography with fluorescence detection.
1987 Apr 24
Multireceptor GABAergic regulation of synaptic communication in amphibian retina.
2001 Jan 1
Effects of central imidazolinergic and alpha2-adrenergic activation on water intake.
2001 Sep
Medicinal chemistry and molecular pharmacology of GABA(C) receptors.
2002 Aug
trans-4-Amino-2-methylbut-2-enoic acid (2-MeTACA) and (+/-)-trans-2-aminomethylcyclopropanecarboxylic acid ((+/-)-TAMP) can differentiate rat rho3 from human rho1 and rho2 recombinant GABA(C) receptors.
2002 Feb
Imidazoline receptors in the heart: characterization, distribution, and regulation.
2002 Jun
Pharmacology of GABA(A) receptors exhibiting different levels of spontaneous activity.
2003 Aug 22
Peripheral GABAB agonists stimulate gastric acid secretion in mice.
2004 Jul
Suppression of different phases of systemic contact hypersensitivity by urocanic acid oxidation products.
2004 Jul-Aug
Coordination sphere vibrations in copper(II), nickel(II) and cobalt(II) complexes with 4-imidazoleacetic acid; metal isotope, deuteration, and density functional study.
2004 Jun
Activation of single heteromeric GABA(A) receptor ion channels by full and partial agonists.
2004 Jun 1
Mutations of the 2' proline in the M2 domain of the human GABAC rho1 subunit alter agonist responses.
2004 May
Kinetic analysis of the role of histidine chloramines in hypochlorous acid mediated protein oxidation.
2005 May 17
A catalytic mechanism revealed by the crystal structures of the imidazolonepropionase from Bacillus subtilis.
2006 Dec 1
OFF response of bullfrog cones is shaped by terminal ionotropic GABA receptors.
2006 Dec 11
Rapid determination of histamine and its metabolites in mice hair by ultra-performance liquid chromatography with time-of-flight mass spectrometry.
2006 Nov 3
High pH accelerates GABA deactivation on perch-rho1B receptors.
2006 Nov 3
An ionotropic GABA receptor with novel pharmacology at bullfrog cone photoreceptor terminals.
2006-2007
5-Substituted imidazole-4-acetic acid analogues: synthesis, modeling, and pharmacological characterization of a series of novel gamma-aminobutyric acid(C) receptor agonists.
2007 Aug 23
Hair analysis of histamine and several metabolites in C3H/HeNCrj mice by ultra performance liquid chromatography with electrospray ionization time-of-flight mass spectrometry (UPLC-ESI-TOF-MS): influence of hair cycle and age.
2007 Mar
Metabolic signature of breast cancer cell line MCF-7: profiling of modified nucleosides via LC-IT MS coupling.
2007 Nov 29
High-throughput phenotypic characterization of Pseudomonas aeruginosa membrane transport genes.
2008 Oct 3
Postelicitation model of allergic contact dermatitis for predicting the efficacy of topical drugs.
2009 Jan
Characterizing metabolic inhibition using electrochemical enzyme/DNA biosensors.
2009 Jan 15
Effects of 4-methylimidazole on cerebral glutamate decarboxylase activity and specific GABA receptor binding in mice.
2009 Mar
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:44:02 GMT 2023
Edited
by admin
on Fri Dec 15 19:44:02 GMT 2023
Record UNII
ET7A74ROAO
Record Status Validated (UNII)
Record Version
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Name Type Language
IMIDAZOLEACETIC ACID HYDROCHLORIDE
Systematic Name English
1H-IMIDAZOLE-5-ACETIC ACID, HYDROCHLORIDE (1:1)
Common Name English
1H-IMIDAZOLE-5-ACETIC ACID HYDROCHLORIDE
Systematic Name English
IMIDAZOLE-4-ACETIC ACID, MONOHYDROCHLORIDE
Common Name English
(1H-IMIDAZOL-5-YL)ACETIC ACID HYDROCHLORIDE
Systematic Name English
(1H-IMIDAZOL-4-YL)ACETIC ACID HYDROCHLORIDE
Systematic Name English
IMIDAZOLE-4-ACETIC ACID HYDROCHLORIDE
Systematic Name English
4-IMIDAZOLEACETIC ACID HYDROCHLORIDE
Systematic Name English
1H-IMIDAZOLE-4-ACETIC ACID, HYDROCHLORIDE
Common Name English
IMIDAZOL-4-ACETIC ACID HYDROCHLORIDE
Systematic Name English
1H-IMIDAZOLE-4-ACETIC ACID, MONOHYDROCHLORIDE
Common Name English
Code System Code Type Description
PUBCHEM
145685
Created by admin on Fri Dec 15 19:44:02 GMT 2023 , Edited by admin on Fri Dec 15 19:44:02 GMT 2023
PRIMARY
FDA UNII
ET7A74ROAO
Created by admin on Fri Dec 15 19:44:02 GMT 2023 , Edited by admin on Fri Dec 15 19:44:02 GMT 2023
PRIMARY
ECHA (EC/EINECS)
221-840-6
Created by admin on Fri Dec 15 19:44:02 GMT 2023 , Edited by admin on Fri Dec 15 19:44:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID00186237
Created by admin on Fri Dec 15 19:44:02 GMT 2023 , Edited by admin on Fri Dec 15 19:44:02 GMT 2023
PRIMARY
CAS
3251-69-2
Created by admin on Fri Dec 15 19:44:02 GMT 2023 , Edited by admin on Fri Dec 15 19:44:02 GMT 2023
PRIMARY