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

Details

Stereochemistry ACHIRAL
Molecular Formula C7H3I2NO
Molecular Weight 370.9138
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IOXYNIL

SMILES

OC1=C(I)C=C(C=C1I)C#N

InChI

InChIKey=NRXQIUSYPAHGNM-UHFFFAOYSA-N
InChI=1S/C7H3I2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H

HIDE SMILES / InChI

Molecular Formula C7H3I2NO
Molecular Weight 370.9138
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Analysis of acidic pesticides using in situ derivatization with alkylchloroformate and solid-phase microextraction (SPME) for GC-MS.
2001 Sep
The effects of endocrine-disrupting chemicals on thyroid hormone binding to Xenopus laevis transthyretin and thyroid hormone receptor.
2002 Dec
Off-line solid-phase microextraction and capillary electrophoresis mass spectrometry to determine acidic pesticides in fruits.
2003 Feb 1
Movement of pendimethalin, ioxynil and soil particles to field drainage tiles.
2003 Jan
Endocrine disrupting chemicals: interference of thyroid hormone binding to transthyretins and to thyroid hormone receptors.
2003 Jan 31
Bioaccumulation and toxicity of sediment associated herbicides (ioxynil, pendimethalin, and bentazone) in Lumbriculus variegatus (Oligochaeta) and Chironomus riparius (Insecta).
2003 Nov
The effect of endocrine disrupting chemicals on thyroid hormone binding to Japanese quail transthyretin and thyroid hormone receptor.
2003 Oct 15
Characteristics of 3,5,3'-triiodothyronine (T3)-uptake system of tadpole red blood cells: effect of endocrine-disrupting chemicals on cellular T3 response.
2004 Dec
Detection of thyroid system-disrupting chemicals using in vitro and in vivo screening assays in Xenopus laevis.
2005 Dec
Quality control of photosystem II. Cleavage of reaction center D1 protein in spinach thylakoids by FtsH protease under moderate heat stress.
2006 Aug 4
Herbicide binding and thermal stability of photosystem II isolated from Thermosynechococcus elongatus.
2006 Feb
Proximity to crops and residential exposure to agricultural herbicides in iowa.
2006 Jun
Spatial and geographical variations of urban, suburban and rural atmospheric concentrations of phenols and nitrophenols.
2006 Mar
Disruption of thyroid hormone binding to sea bream recombinant transthyretin by ioxinyl and polybrominated diphenyl ethers.
2007 Aug
Demonstrating formation of potentially persistent transformation products from the herbicides bromoxynil and ioxynil using liquid chromatography-tandem mass spectrometry (LC-MS/MS).
2007 Feb
Interaction of diethylstilbestrol and ioxynil with transthyretin in chicken serum.
2008 Apr
Microbial degradation of the benzonitrile herbicides dichlobenil, bromoxynil and ioxynil in soil and subsurface environments--insights into degradation pathways, persistent metabolites and involved degrader organisms.
2008 Jul
Herbicide effect on the hydrogen-bonding interaction of the primary quinone electron acceptor QA in photosystem II as studied by Fourier transform infrared spectroscopy.
2008 Oct-Dec
The genome of Nectria haematococca: contribution of supernumerary chromosomes to gene expansion.
2009 Aug
Disruption of the thyroid system by diethylstilbestrol and ioxynil in the sea bream (Sparus aurata).
2009 May 17
Multi-residue determination of phenolic and salicylanilide anthelmintics and related compounds in bovine kidney by liquid chromatography-tandem mass spectrometry.
2009 Nov 13
Inhibition of connexin 43 gap junction channels by the endocrine disruptor ioxynil.
2010 Aug 15
Transgene x environment interactions in genetically modified wheat.
2010 Jul 12
Structures and binding sites of phenolic herbicides in the Q(B) pocket of photosystem II.
2010 Jul 6
Light-induced changes within photosystem II protects Microcoleus sp. in biological desert sand crusts against excess light.
2010 Jun 8
Hydrolysis of benzonitrile herbicides by soil actinobacteria and metabolite toxicity.
2010 Sep
Unique cellular effect of the herbicide bromoxynil revealed by electrophysiological studies using characean cells.
2010 Sep
Ioxynil and tetrabromobisphenol A suppress thyroid-hormone-induced activation of transcriptional elongation mediated by histone modifications and RNA polymerase II phosphorylation.
2014 Apr
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:56:16 GMT 2023
Edited
by admin
on Fri Dec 15 18:56:16 GMT 2023
Record UNII
8Y734M4V9E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IOXYNIL
HSDB   ISO  
Common Name English
M&B 8873
Code English
IOXYNIL [MI]
Common Name English
4-HYDROXY-3,5-DIIODOBENZONITRILE
Systematic Name English
IOXYNIL [HSDB]
Common Name English
IOXYNIL [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 353200
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
Code System Code Type Description
HSDB
1584
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
FDA UNII
8Y734M4V9E
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
PUBCHEM
15530
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
ALANWOOD
ioxynil
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
MERCK INDEX
m11756
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
CHEBI
81821
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
EPA CompTox
DTXSID8022161
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
ECHA (EC/EINECS)
216-881-1
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
MESH
C008161
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY
CAS
1689-83-4
Created by admin on Fri Dec 15 18:56:16 GMT 2023 , Edited by admin on Fri Dec 15 18:56:16 GMT 2023
PRIMARY