Page last updated: 2024-12-05

isoprocarb

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

Cross-References

ID SourceID
PubMed CID17517
CHEMBL ID2251586
CHEBI ID38505
SCHEMBL ID64155
MeSH IDM0179476

Synonyms (88)

Synonym
2-(propan-2-yl)phenyl n-methylcarbamate
2631-40-5
isoprocarb
o-isopropylphenyl methylcarbamate
nsc191479
o-isopropylphenyl n-methylcarbamate
hytox
o-cumenyl methylcarbamate
wln: 1yr bovm1
oms 32
ent 25670
carbamic acid, o-isopropylphenyl ester
o-cumenyl n-methylcarbamate
2-isopropylphenyl methylcarbamate
bay 39731
2-isopropylphenyl n-methylcarbamate
khe 0145
bayer 39,731
carbamic acid, o-cumenyl ester
ro 7-5050
o-isopropylphenol methylcarbamate
isopropylphenol methylcarbamate
ppc 3
bay 105807
mipcine
nsc-191479
etrofolan
mipcin
phenol, 2-(1-methylethyl)-, methylcarbamate
carbamic acid, methyl-, o-cumenyl ester
carbamic acid, methyl-, 2-(1-methylethyl)phenyl ester
einecs 220-114-6
isoprocarb [bsi:iso]
ai3-25670
nsc 191479
oms-32
isoprocarbe [iso-french]
phenol, o-isopropyl-, methylcarbamate
bayer 39731
epa pesticide chemical code 512300
isoprocarbe
carbamic acid, methyl-, o-isopropylphenyl ester
brn 1875020
caswell no. 512b
mipsin
n-methyl-2-isopropylphenylcarbam
CHEBI:38505 ,
2-(propan-2-yl)phenyl methylcarbamate
2-(1-methylethyl)phenyl methylcarbamate
2-(1-methylethyl)phenol methylcarbamate
NCGC00160600-01
(2-propan-2-ylphenyl) n-methylcarbamate
qbsjmkiucuggng-uhfffaoysa-
inchi=1/c11h15no2/c1-8(2)9-6-4-5-7-10(9)14-11(13)12-3/h4-8h,1-3h3,(h,12,13)
C18418
phenol, 2-(1-methylethyl)-, 1-(n-methylcarbamate)
4-06-00-03212 (beilstein handbook reference)
unii-714i55qh9k
714i55qh9k ,
cas-2631-40-5
NCGC00255918-01
dtxsid6042072 ,
dtxcid4022072
tox21_301361
AKOS006229087
FT-0603616
CHEMBL2251586
SCHEMBL64155
isoprocarb [iso]
bay-39731
ent-25670
2-(1-methylethyl)phenyl n-methylcarbamate
n-methyl-2-isopropylphenylcarbamate
isopropyl phenylmethyl carbamate
methylcarbamic acid, o-cumenyl ester
2-(1-methylethyl)-phenol methyl-carbamate
isoprocarb, pestanal(r), analytical standard
etrolan
2-(1-methylethyl)phenyl methylcarbamate, 9ci
mipc, jmaf
cumenyl n-methylcarbamate
isoprocarb, bsi, iso
J-016376
Q27117880
CAA63140
AS-80767
CS-0012844
HY-B0830

Research Excerpts

Overview

Isoprocarb is a widely used carbamate insecticide in agriculture and aquaculture.

ExcerptReferenceRelevance
"Isoprocarb is a widely used carbamate insecticide in agriculture and aquaculture. "( Isoprocarb causes neurotoxicity of zebrafish embryos through oxidative stress-induced apoptosis.
Han, X; Hu, C; Liu, Y; Mao, H; Wang, S; Xu, X; Yu, T; Zhang, H, 2022
)
3.61

Toxicity

ExcerptReferenceRelevance
" The toxic effects as observed 10 or 21 days after medication include a statistically significant reduction in haemoglobin (Hb) content, haematocrit (Ht), protein and serum glutamate pyruvate transaminase (SGPT), and an increase in glucose, serum glutamate oxaloacetate transaminase (SGOT) and serum acid phosphatase (SAP) activities of male and female chicken."( Haematological and hepatotoxic effects of isoprocarb in chicken.
Mahboob, M; Mustafa, M; Rahman, MF; Siddiqui, MK, 1990
)
0.54
" Overuse of isoprocarb always leaves toxic residues in soil and water, however, the potential ecotoxicity of isoprocarb to organisms is still confusing."( Isoprocarb causes neurotoxicity of zebrafish embryos through oxidative stress-induced apoptosis.
Han, X; Hu, C; Liu, Y; Mao, H; Wang, S; Xu, X; Yu, T; Zhang, H, 2022
)
2.54

Dosage Studied

ExcerptRelevanceReference
" A significant inhibition of RBC acetylcholinesterase was noticed after 21 days of dosing only at the high dose (150 mg kg-1) in hens."( Haematological and hepatotoxic effects of isoprocarb in chicken.
Mahboob, M; Mustafa, M; Rahman, MF; Siddiqui, MK, 1990
)
0.54
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
EC 3.1.1.7 (acetylcholinesterase) inhibitorAn EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of enzyme acetylcholinesterase (EC 3.1.1.7), which helps breaking down of acetylcholine into choline and acetic acid.
carbamate insecticideDerivatives of carbamic acid with insecticidal properties of general formula ROC(=O)NR(1)R(2), where ROH is an alcohol, oxime, or phenol and R(1) is hydrogen or methyl. Like organophosphate insecticides, they are cholinesterase inhibitors, but carbamate insecticides differ in action from the organophosphates in that the inhibitory effect on cholinesterase is generally brief.
agrochemicalAn agrochemical is a substance that is used in agriculture or horticulture.
[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 (1)

ClassDescription
carbamate esterAny ester of carbamic acid or its N-substituted derivatives.
[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 (4)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
acetylcholinesteraseHomo sapiens (human)Potency18.09530.002541.796015,848.9004AID1347395; AID1347397; AID1347398; AID1347399
RAR-related orphan receptor gammaMus musculus (house mouse)Potency76.95880.006038.004119,952.5996AID1159521
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency54.48270.001022.650876.6163AID1224839
retinoid X nuclear receptor alphaHomo sapiens (human)Potency48.96620.000817.505159.3239AID1159527; AID1159531
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (23)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (4.35)18.2507
2000's6 (26.09)29.6817
2010's10 (43.48)24.3611
2020's6 (26.09)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 27.94

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 Index27.94 (24.57)
Research Supply Index3.22 (2.92)
Research Growth Index5.30 (4.65)
Search Engine Demand Index47.56 (26.88)
Search Engine Supply Index3.00 (0.95)

This Compound (27.94)

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%
Other24 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]