Page last updated: 2024-12-06

imazaquin

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

Description

imazaquin: RN given refer to parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

imazaquin : A racemate comprising equimolar amounts of (R)- and (S)-imazaquin. It is a pre- and post-emergence herbicide used for the control of grasses and broad-leaved weeds. [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]

2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid : A quinolinemonocarboxylic acid that is quinoline-3-carboxylic acid which is substituted by a 4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl group at position 2. [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 CID54739
CHEMBL ID1447880
CHEBI ID147361
CHEBI ID5869
SCHEMBL ID18804
MeSH IDM0161402

Synonyms (73)

Synonym
caswell no. 003c
scepter herbicide
epa pesticide chemical code 128840
imazaquin [bsi:iso]
brn 5450078
2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1h-imidazol-2-yl)-3-quinolinecarboxylic acid
2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)quinoline-3-carboxylic acid
3-quinolinecarboxylic acid, 2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1h-imidazol-2-yl)-
2-(5-isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl)-3-quinolinecarboxylic acid
ac 252214
hsdb 6677
imazaquine [iso-french]
3-quinolinecarboxylic acid, 2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1h-imidazol-2-yl]-
2-(4-isopropyl-4-methyl-5-oxo-1h-imidazol-2-yl)quinoline-3-carboxylic acid
MLS000080369
2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1h-imidazol-2-yl)quinoline-3-carboxylic acid
81335-37-7
imazaquin
C05076
NCGC00163758-01
smr000059314
NCGC00163758-02
2,6-pyridinedicarboxylicacid
2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)quinoline-3-carboxylic acid
CHEBI:147361
2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1h-imidazol-2-yl]quinoline-3-carboxylic acid
2-(4-methyl-5-oxidanylidene-4-propan-2-yl-1h-imidazol-2-yl)quinoline-3-carboxylic acid
A840099
2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)-3-quinolinecarboxylic acid
AKOS004910001
NCGC00065519-02
NCGC00065519-03
NCGC00065519-04
NCGC00065519-05
imazaquin acid
STK711163
8lzy7c31xa ,
unii-8lzy7c31xa
imazaquine
NCGC00254700-01
cas-81335-37-7
dtxcid904152
tox21_202008
NCGC00259557-01
tox21_300796
dtxsid3024152 ,
BBL010099
HMS2336H03
2-(5-isopropyl-5-methyl-4-oxo-2-imidazolin-2-yl)-3- quinolinecarboxylic acid
imazaquin [iso]
2-(4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1h-imidazol- 2-yl)-3-quinolinecarboxylic acid
imazaquin, (+/-)-
2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-3-quinolinecarboxylic acid
imazaquin [mi]
2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)quinoline-3- carboxylic acid
3-quinolinecarboxylic acid, 2-(4,5-dihydro-4-methyl-4-(1- methylethyl)-5-oxo-1h-imidazol-2-yl)-
image (pesticide)
imazaquine [hsdb]
SCHEMBL18804
CHEMBL1447880
chebi:5869
2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)3-quinolinecarboxylic acid
2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1h-imidazol-2-yl)-3-quinolinecarboxylic acid
imazaquin, pestanal(r), analytical standard
bdbm50486241
FT-0706952
HY-W040189
VS-02316
Q15303948
mfcd00778521
CS-W020929
2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1h-imidazol-2-yl]-3-quinolinecarboxylicacid
AKOS040741872

Research Excerpts

Overview

Imazaquin is a chiral herbicide which displays high mobility in soils.

ExcerptReferenceRelevance
"Imazaquin is a chiral herbicide which displays high mobility in soils. "( A clay-based formulation of the herbicide imazaquin containing exclusively the biologically active enantiomer.
Celis, R; Cornejo, J; López-Cabeza, R; Poiger, T, 2019
)
2.22

Bioavailability

ExcerptReferenceRelevance
" The concentrations that inhibited growth by 50% (IC50) of FLU and IMA individually and their combination estimated from the herbicide concentrations in soil pore water notably differed from those based on the amended concentrations, due to the decline in bioavailability resulting from adsorption of the herbicides onto soil."( Estimating the combined toxicity of flufenacet and imazaquin to sorghum with pore water herbicide concentration.
Lin, D; Wang, D; Yu, Y; Zhang, Q; Zheng, Y, 2016
)
0.69

Dosage Studied

ExcerptRelevanceReference
" In this study, dose-response of the SU-resistant accession was compared with that of a SU-susceptible accession at in vivo whole-plant level as well as at in vitro enzymatic level."( Characterization of sulfonylurea-resistant Schoenoplectus juncoides having a target-site Asp(376)Glu mutation in the acetolactate synthase.
Ikeda, H; Kizawa, S; Sada, Y; Yamato, S, 2013
)
0.39
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (3)

ClassDescription
quinolinemonocarboxylic acidAny aromatic carboxylic acid that contains a quinoline moiety that is substituted by one carboxy substituent.
imidazolone
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]

Protein Targets (16)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, Putative fructose-1,6-bisphosphate aldolaseGiardia intestinalisPotency6.29460.140911.194039.8107AID2451
ATAD5 protein, partialHomo sapiens (human)Potency3.66260.004110.890331.5287AID504467
GLI family zinc finger 3Homo sapiens (human)Potency30.88730.000714.592883.7951AID1259369
thyroid stimulating hormone receptorHomo sapiens (human)Potency39.81070.001318.074339.8107AID926
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency24.53460.000657.913322,387.1992AID1259377
farnesoid X nuclear receptorHomo sapiens (human)Potency0.00710.375827.485161.6524AID588527
pregnane X nuclear receptorHomo sapiens (human)Potency79.43280.005428.02631,258.9301AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency55.47320.000229.305416,493.5996AID743075; AID743077
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency19.95260.001024.504861.6448AID588535
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency38.57080.001723.839378.1014AID743083
importin subunit beta-1 isoform 1Homo sapiens (human)Potency63.09575.804836.130665.1308AID540263
snurportin-1Homo sapiens (human)Potency63.09575.804836.130665.1308AID540263
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency54.48270.000627.21521,122.0200AID651741
VprHuman immunodeficiency virus 1Potency14.12541.584919.626463.0957AID651644
survival motor neuron protein isoform dHomo sapiens (human)Potency0.00280.125912.234435.4813AID1458
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Acetolactate synthase, chloroplasticArabidopsis thaliana (thale cress)Ki236.50000.00800.72643.0000AID1083000; AID1083001
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (16)

Assay IDTitleYearJournalArticle
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID1083000Inhibition of Arabidopsis thaliana acetohydroxyacid synthase W574L mutant colorimetric assay2012Journal of agricultural and food chemistry, Aug-29, Volume: 60, Issue:34
Synthesis, crystal structure, in vitro acetohydroxyacid synthase inhibition, in vivo herbicidal activity, and 3D-QSAR of new asymmetric aryl disulfides.
AID1082999Resistance index, ratio of Ki for Arabidopsis thaliana acetohydroxyacid synthase W574L mutant to Ki for wild type Arabidopsis thaliana acetohydroxyacid synthase2012Journal of agricultural and food chemistry, Aug-29, Volume: 60, Issue:34
Synthesis, crystal structure, in vitro acetohydroxyacid synthase inhibition, in vivo herbicidal activity, and 3D-QSAR of new asymmetric aryl disulfides.
AID1083001Inhibition of wild type Arabidopsis thaliana acetohydroxyacid synthase colorimetric assay2012Journal of agricultural and food chemistry, Aug-29, Volume: 60, Issue:34
Synthesis, crystal structure, in vitro acetohydroxyacid synthase inhibition, in vivo herbicidal activity, and 3D-QSAR of new asymmetric aryl disulfides.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (46)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (2.17)18.7374
1990's1 (2.17)18.2507
2000's28 (60.87)29.6817
2010's15 (32.61)24.3611
2020's1 (2.17)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 29.94

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 Index29.94 (24.57)
Research Supply Index3.95 (2.92)
Research Growth Index5.77 (4.65)
Search Engine Demand Index65.56 (26.88)
Search Engine Supply Index3.83 (0.95)

This Compound (29.94)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other51 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]