Page last updated: 2024-09-22

dioxacarb

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

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]

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]