Compounds > dioxacarb
Page last updated: 2024-12-06

dioxacarb

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

Description

dioxacarb: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID23421
CHEMBL ID3188645
CHEBI ID82093
SCHEMBL ID119641
MeSH IDM0062163

Synonyms (62)

Synonym
carbamic acid, methyl-, o-(1,3-dioxolan-2-yl)phenyl ester
phenol, 2-(1,3-dioxolan-2-yl)-, methylcarbamate
elocron 8353
2-(1,3-dioxolan-2-yl)phenyl-n-methylcarbamat [german]
dioxacarb [ansi:bsi:iso]
mcdp
c 8353
ai3-27389
ent 27,389
caswell no. 393a
einecs 230-253-4
dioxacarb
elocron
epa pesticide chemical code 392100
du pont insecticide 1519
ciba c 8353
c-8353 ,
dioxokarb [polish]
carbamic acid, methyl-, o-1,3-dioxolan-2-ylphenyl ester
ciba 8353
famid
rovlinka
nsc 190981
elocron 50wp
brn 1348191
dioxacarbe
2-(1,3-dioxolan-2-yl)phenol methylcarbamate
o-(1,3-dioxolan-2-yl)phenyl methylcarbamate
dioxacarbe [iso-french]
du pont 1519
dioxocarb
2-(1,3-dioxolan-2-yl)phenyl methylcarbamate
[2-(1,3-dioxolan-2-yl)phenyl] n-methylcarbamate
C18953
6988-21-2
dtxcid0021886
NCGC00255496-01
cas-6988-21-2
tox21_302420
dtxsid2041886 ,
2-(1,3-dioxolan-2-yl)phenyl-n-methylcarbamat
698bek3133 ,
5-19-02-00547 (beilstein handbook reference)
unii-698bek3133
dioxokarb
AKOS015902513
dioxacarb [iso]
phenol, 2-(1,3-dioxolan-2-yl)-, 1-(n-methylcarbamate)
2-(1,3-dioxolane-2-yl)-phenyl n-methylcarbamate
2-(1,3-dioxolan-2-yl)phenyl n-methylcarbamate
du pont-1519
elocron-8353
SCHEMBL119641
CHEBI:82093 ,
2-(1,3-dioxolan-2-yl)phenyl methylcarbamate #
elecron 50
2-(1,3-dioxolane-2-yl)phenyl n-methylcarbamate
CHEMBL3188645
pesticide3_dioxacarb_c11h13no4_phenol, 2-(1,3-dioxolan-2-yl)-, methylcarbamate
FT-0667620
Q22807435
o-(1,3-dioxalan-2-yl)phenyl methylcarbamate
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
benzenesAny benzenoid aromatic compound consisting of the benzene skeleton and its 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)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency0.54210.006038.004119,952.5996AID1159521
AR proteinHomo sapiens (human)Potency46.69430.000221.22318,912.5098AID743035; AID743036
aryl hydrocarbon receptorHomo sapiens (human)Potency59.11880.000723.06741,258.9301AID743085; AID743122
heat shock protein beta-1Homo sapiens (human)Potency21.76810.042027.378961.6448AID743210
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (40.00)18.7374
1990's2 (40.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 23.88

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 Index23.88 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.32 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (23.88)

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%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
carbamates
[no description available]		3.0850amino-acid anion
carbofuran
Carbofuran: A cholinesterase inhibitor that is used as a systemic insecticide, an acaricide, and nematocide. (From Merck Index, 11th ed)		1.96101-benzofurans;
carbamate ester		acaricide;
agrochemical;
avicide;
carbamate insecticide;
EC 3.1.1.7 (acetylcholinesterase) inhibitor;
EC 3.1.1.8 (cholinesterase) inhibitor;
nematicide
phosalone
phosalone: structure. phosalone : A member of the class of 1,3-benzoxazoles carrying a [(diethoxyphosphorothioyl)sulfanyl]methyl group at the nitrogen atom, an oxo group at position 2 and a chloro group at position 6. It is an organothiophosphate insecticide.		1.96101,3-benzoxazoles;
carbamate ester;
organochlorine insecticide;
organothiophosphate insecticide		acaricide;
agrochemical;
EC 3.1.1.7 (acetylcholinesterase) inhibitor;
EC 3.1.1.8 (cholinesterase) inhibitor
propoxur
Propoxur: A carbamate insecticide.. propoxur : A carbamate ester that is phenyl methylcarbamate substituted at position 2 by a propan-2-yloxy group.		1.9610aromatic ether;
carbamate ester		acaricide;
agrochemical;
carbamate insecticide;
EC 3.1.1.7 (acetylcholinesterase) inhibitor
carbaryl
Carbaryl: A carbamate insecticide and parasiticide. It is a potent anticholinesterase agent belonging to the carbamate group of reversible cholinesterase inhibitors. It has a particularly low toxicity from dermal absorption and is used for control of head lice in some countries.. carbaryl : A carbamate ester obtained by the formal condensation of 1-naphthol with methylcarbamic acid.		1.9610carbamate ester;
naphthalenes		acaricide;
agrochemical;
carbamate insecticide;
EC 3.1.1.7 (acetylcholinesterase) inhibitor;
EC 3.1.1.8 (cholinesterase) inhibitor;
plant growth retardant
quinalphos
quinalphos: RN given refers to cpd with locant for quinoxalinyl group in position 2; structure		1.9610organic thiophosphate;
organothiophosphate insecticide		acaricide;
agrochemical;
EC 3.1.1.7 (acetylcholinesterase) inhibitor
iodofenphos
[no description available]		1.9710organic thiophosphate
permethrin
hemoglobin Atlanta-Coventry: Leu replaced by Pro at beta75 and Leu deleted at beta141		2.3720cyclopropanecarboxylate ester;
cyclopropanes		agrochemical;
ectoparasiticide;
pyrethroid ester acaricide;
pyrethroid ester insecticide;
scabicide
tetramethrin
tetramethrin: structure		1.9610cyclopropanecarboxylate ester;
maleimides;
phthalimide insecticide		pyrethroid ester insecticide
thiofanox
thiofanox: shows potential systemic & contact insecticidal properties against certain phytophagous pests; structure		2.0810
propetamphos
[no description available]		1.9710isopropyl ester;
organophosphate insecticide;
phosphoramidate ester		agrochemical;
EC 3.1.1.7 (acetylcholinesterase) inhibitor
n-methylcarbamate
N-methylcarbamate: RN given refers to parent cpd		1.9610amino-acid anion
pyrethrins
[no description available]		2.3720
ConditionIndicatedRelationship StrengthStudiesTrials