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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6N2O2
Molecular Weight 126.1133
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IMIDAZOLE-2-ACETIC ACID

SMILES

OC(=O)CC1=NC=CN1

InChI

InChIKey=WUJUYHMGDPTLMG-UHFFFAOYSA-N
InChI=1S/C5H6N2O2/c8-5(9)3-4-6-1-2-7-4/h1-2H,3H2,(H,6,7)(H,8,9)

HIDE SMILES / InChI

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
Nanosegregated composites of an imidazolium salt and a layered inorganic compound: organization of both anions and cations in interlayer space.
2010-11
Extracellular Paracoccidioides brasiliensis phospholipase B involvement in alveolar macrophage interaction.
2010-09-15
Staging of Alzheimer's pathology in triple transgenic mice: a light and electron microscopic analysis.
2010-07-15
A single step purification for autolytic zinc proteinases.
2010-01-01
Expression and purification of full-length recombinant PrP of high purity.
2008
Highly Efficient Phosphopeptide Enrichment by Calcium Phosphate Precipitation Combined with Subsequent IMAC Enrichment.
2007-11
Electromigration of a heteroconjugated imidazole-acetate complex in ACN.
2007-10
Optimizing TiO2-based phosphopeptide enrichment for automated multidimensional liquid chromatography coupled to tandem mass spectrometry.
2007-06-15
Rat alpha6beta2delta GABAA receptors exhibit two distinct and separable agonist affinities.
2007-06-15
Characterization of phosphorylation sites on Tpl2 using IMAC enrichment and a linear ion trap mass spectrometer.
2007-06
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.
2007-03
Variation of atomic charges on proton transfer in strong hydrogen bonds: the case of anionic and neutral imidazole-acetate complexes.
2006-11-15
Comprehensive identification of phosphorylation sites in postsynaptic density preparations.
2006-05
Enhanced phosphopeptide isolation by Fe(III)-IMAC using 1,1,1,3,3,3-hexafluoroisopropanol.
2005-11
Kinetic analysis of the role of histidine chloramines in hypochlorous acid mediated protein oxidation.
2005-05-17
Charged residues at the 2' position of human GABAC rho 1 receptors invert ion selectivity and influence open state probability.
2004-12-24
Peripheral GABAB agonists stimulate gastric acid secretion in mice.
2004-07
Coordination sphere vibrations in copper(II), nickel(II) and cobalt(II) complexes with 4-imidazoleacetic acid; metal isotope, deuteration, and density functional study.
2004-06
Production and characterization of oil-in-water emulsions containing droplets stabilized by beta-lactoglobulin-pectin membranes.
2003-10-22
Theoretical studies of IMAC interfacial phenomena for the production of protein C.
2003
Towards crystallization of hydrophobic myelin glycoproteins: P0 and PASII/PMP22.
2002-12
Identification of a tyrosine in the agonist binding site of the homomeric rho1 gamma-aminobutyric acid (GABA) receptor that, when mutated, produces spontaneous opening.
2002-11-15
A novel affinity gene fusion system allowing protein A-based recovery of non-immunoglobulin gene products.
2002-10-09
Medicinal chemistry and molecular pharmacology of GABA(C) receptors.
2002-08
Urinary histamine metabolite elevations during experimental influenza infection.
2001-10
Oxidative breakdown and conversion of urocanic acid isomers by hydroxyl radical generating systems.
2001-06-15
Studies on the possibility of histidine biosynthesis from histodinol, imidazolepyruvic acid, imidazoleacetica acid, and imidazolelactic acid by mixed ruminal bacteria, protozoa, and their mixture in vitro.
2001-03
In vitro catabolism of histidine by mixed rumen bacteria and protozoa.
2001-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:26:49 GMT 2025
Edited
by admin
on Mon Mar 31 21:26:49 GMT 2025
Record UNII
Y47072X58S
Record Status Validated (UNII)
Record Version
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Name Type Language
1H-IMIDAZOLE-2-ACETIC ACID
Preferred Name English
IMIDAZOLE-2-ACETIC ACID
Systematic Name English
2-(1H-IMIDAZOL-2-YL)ACETIC ACID
Systematic Name English
2-IMIDAZOLEACETIC ACID
Systematic Name English
Code System Code Type Description
FDA UNII
Y47072X58S
Created by admin on Mon Mar 31 21:26:49 GMT 2025 , Edited by admin on Mon Mar 31 21:26:49 GMT 2025
PRIMARY
CAS
189502-92-9
Created by admin on Mon Mar 31 21:26:49 GMT 2025 , Edited by admin on Mon Mar 31 21:26:49 GMT 2025
PRIMARY
PUBCHEM
17935379
Created by admin on Mon Mar 31 21:26:49 GMT 2025 , Edited by admin on Mon Mar 31 21:26:49 GMT 2025
PRIMARY
EPA CompTox
DTXSID90172361
Created by admin on Mon Mar 31 21:26:49 GMT 2025 , Edited by admin on Mon Mar 31 21:26:49 GMT 2025
PRIMARY