Page last updated: 2024-12-07

methylimidazoleacetic acid

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

methylimidazoleacetic acid: urinary metabolite of histamine & end product of histamine metabolism; RN given refers to parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

1-methyl-4-imidazoleacetic acid : A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens has been replaced by a 1-methyl-1H-imidazol-4-yl group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

1-methyl-4-imidazoleacetate : A monocarboxylic acid anion that is the conjugate base of 1-methyl-4-imidazoleacetic acid, obtained by deprotonation of the carboxy group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID75810
CHEBI ID1606
SCHEMBL ID876467
MeSH IDM0043367

Synonyms (53)

Synonym
nsc66355
nsc-66355
methylimidazoleacetate
C05828
1-methyl-4-imidazoleacetic acid
tele-methylimidazoleacetic acid
1-methylimidazole-4-acetate
methylimidazoleacetic acid
2625-49-2
1-methyl-4-imidazoleacetate
imidazole-4-acetic acid, 1-methyl-
8D53E49D-B4B8-4F6B-86C8-B081DCB0AC38
1,4-methyl-imidazoleacetic acid
2-(1-methylimidazol-4-yl)acetic acid
2-(1-methyl-1h-imidazol-4-yl)acetic acid
A5220
(1-methyl-1h-imidazol-4-yl)-acetic acid
AKOS006239534
1h-imidazole-4-acetic acid, 1-methyl-
nsc 66355
hsdb 8464
unii-ekp351892f
ekp351892f ,
CHEBI:1606
(1-methyl-1h-imidazol-4-yl)acetic acid
n-methylimidazoleacetate
n-methylimidazoleacetic acid
mima
n-methylimidazole-4-acetic acid
1-methylimidazoleacetic acid
SCHEMBL876467
ZHCKPJGJQOPTLB-UHFFFAOYSA-N
1-methyl-4imidazoleacetic acid
1-methylimidazole-4-acetic acid
DTXSID30180884
1-methyl-1h-imidazole-4-acetate
miaa
1-methyl-1h-imidazole-4-acetic acid
1,4-methylimidazoleacetate
methylimidazole acetate
tele-methylimidazoleacetate
1-methyl-13c, d3-1h-imidazol-4-yl acetic acid
FT-0735633
DS-3866
mfcd08668290
Q27105479
n tau-methylimidazoleacetic acid
SB21943
P10612
EN300-816432
CS-0008620
PD044657
2-(1-methyl-1h-imidazol-4-yl)aceticacid

Research Excerpts

Overview

1,4‑methylimidazoleacetic acid (MIAA) is an endogenous biomarker and metabolite of histamine turnover.

ExcerptReferenceRelevance
"1,4‑methylimidazoleacetic acid (MIAA) is an endogenous biomarker and metabolite of histamine turnover."( Population histamine burden assessed using wastewater-based epidemiology: The association of 1,4‑methylimidazole acetic acid and fexofenadine.
Choi, PM; Jiang, G; Li, J; Mueller, JF; O'Brien, JW; Thomas, KV, 2018
)
0.96
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
GABA agonistA drug that binds to and activates gamma-aminobutyric acid receptors.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
imidazolesA five-membered organic heterocycle containing two nitrogen atoms at positions 1 and 3, or any of its derivatives; compounds containing an imidazole skeleton.
monocarboxylic acidAn oxoacid containing a single carboxy group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (4)

PathwayProteinsCompounds
Histidine Metabolism1735
Histidinemia1735
Histidine degradation ( Histidine degradation )2326
NAD+ + 3-Methyl-imidazole acetaldehyde + H2O = NADH + 3-Methyl-imidazole-acetic acid ( Histidine degradation )45

Research

Studies (95)

TimeframeStudies, This Drug (%)All Drugs %
pre-199050 (52.63)18.7374
1990's21 (22.11)18.2507
2000's11 (11.58)29.6817
2010's12 (12.63)24.3611
2020's1 (1.05)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 17.39

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index17.39 (24.57)
Research Supply Index4.62 (2.92)
Research Growth Index4.37 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (17.39)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials4 (4.17%)5.53%
Reviews4 (4.17%)6.00%
Case Studies8 (8.33%)4.05%
Observational0 (0.00%)0.25%
Other80 (83.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]