U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C13H13Cl2N3O3
Molecular Weight 330.167
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IPRODIONE

SMILES

CC(C)NC(=O)N1CC(=O)N(C1=O)C2=CC(Cl)=CC(Cl)=C2

InChI

InChIKey=ONUFESLQCSAYKA-UHFFFAOYSA-N
InChI=1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)

HIDE SMILES / InChI

Molecular Formula C13H13Cl2N3O3
Molecular Weight 330.167
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A concentration addition model to assess activation of the pregnane X receptor (PXR) by pesticide mixtures found in the French diet.
2014-09
A novel MDCKII in vitro model for assessing ABCG2-drug interactions and regulation of ABCG2 transport activity in the caprine mammary gland by environmental pollutants and pesticides.
2014-04
Genotoxicity of pesticide mixtures present in the diet of the French population.
2012-04
Impact of environmental chemicals on key transcription regulators and correlation to toxicity end points within EPA's ToxCast program.
2010-03-15
Cumulative and antagonistic effects of a mixture of the antiandrogens vinclozolin and iprodione in the pubertal male rat.
2009-09
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Molecular mechanism of the aryl hydrocarbon receptor activation by the fungicide iprodione in rainbow trout (Oncorhynchus mykiss) hepatocytes.
2005-04-30
Cytotoxicity and transcriptional activation of stress genes in human liver carcinoma (HepG2) cells exposed to iprodione.
2004-03
Effects of currently used pesticides in the AhR-CALUX assay: comparison between the human TV101L and the rat H4IIE cell line.
2003-12-15
Effects of currently used pesticides in assays for estrogenicity, androgenicity, and aromatase activity in vitro.
2002-02-15
Degradation of iprodione by a soil Arthrobacter-like strain.
1995-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:06:30 GMT 2025
Edited
by admin
on Mon Mar 31 19:06:30 GMT 2025
Record UNII
S3AYV2A6EU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHIPCO-26019
Preferred Name English
IPRODIONE
HSDB   ISO   MI  
Common Name English
IPRODIONE [HSDB]
Common Name English
PROMIDIONE
Common Name English
FA-2071
Code English
IPRODIONE [MI]
Common Name English
3-(3,5-DICHLOROPHENYL)-N-(1-METHYLETHYL)-2,4-DIOXO-1-IMIDAZOLIDINECARBOXAMIDE
Systematic Name English
ROVRAL
Brand Name English
LFA-2043
Code English
NRC-910
Code English
IPRODIONE [ISO]
Common Name English
3-(3,5-DICHLOROPHENYL)-N-ISOPROPYL-2,4-DIOXOIMIDAZOLIDINE-1-CARBOXAMIDE
Systematic Name English
RP-26019
Code English
GLYCOPHENE
Common Name English
ROP-500F
Code English
Classification Tree Code System Code
EPA PESTICIDE CODE 109801
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID3024154
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
253-178-9
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
MESH
C033148
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
WIKIPEDIA
IPRODIONE
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
HSDB
6855
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
CAS
36734-19-7
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
CHEBI
28909
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
PUBCHEM
37517
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
FDA UNII
S3AYV2A6EU
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
ALANWOOD
iprodione
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY
MERCK INDEX
m6391
Created by admin on Mon Mar 31 19:06:30 GMT 2025 , Edited by admin on Mon Mar 31 19:06:30 GMT 2025
PRIMARY Merck Index