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Details

Stereochemistry ACHIRAL
Molecular Formula C7H2I2NO.Na
Molecular Weight 392.8956
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IOXYNIL-SODIUM

SMILES

[Na+].[O-]C1=C(I)C=C(C=C1I)C#N

InChI

InChIKey=QGKPUZOFTJQTHL-UHFFFAOYSA-M
InChI=1S/C7H3I2NO.Na/c8-5-1-4(3-10)2-6(9)7(5)11;/h1-2,11H;/q;+1/p-1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Ioxynil and tetrabromobisphenol A suppress thyroid-hormone-induced activation of transcriptional elongation mediated by histone modifications and RNA polymerase II phosphorylation.
2014-04
Hydrolysis of benzonitrile herbicides by soil actinobacteria and metabolite toxicity.
2010-09
Unique cellular effect of the herbicide bromoxynil revealed by electrophysiological studies using characean cells.
2010-09
Inhibition of connexin 43 gap junction channels by the endocrine disruptor ioxynil.
2010-08-15
Transgene x environment interactions in genetically modified wheat.
2010-07-12
Structures and binding sites of phenolic herbicides in the Q(B) pocket of photosystem II.
2010-07-06
Light-induced changes within photosystem II protects Microcoleus sp. in biological desert sand crusts against excess light.
2010-06-08
Multi-residue determination of phenolic and salicylanilide anthelmintics and related compounds in bovine kidney by liquid chromatography-tandem mass spectrometry.
2009-11-13
The genome of Nectria haematococca: contribution of supernumerary chromosomes to gene expansion.
2009-08
Disruption of the thyroid system by diethylstilbestrol and ioxynil in the sea bream (Sparus aurata).
2009-05-17
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.
2008-07
Interaction of diethylstilbestrol and ioxynil with transthyretin in chicken serum.
2008-04
Herbicide effect on the hydrogen-bonding interaction of the primary quinone electron acceptor QA in photosystem II as studied by Fourier transform infrared spectroscopy.
2007-12-29
Disruption of thyroid hormone binding to sea bream recombinant transthyretin by ioxinyl and polybrominated diphenyl ethers.
2007-08
Demonstrating formation of potentially persistent transformation products from the herbicides bromoxynil and ioxynil using liquid chromatography-tandem mass spectrometry (LC-MS/MS).
2007-02
Quality control of photosystem II. Cleavage of reaction center D1 protein in spinach thylakoids by FtsH protease under moderate heat stress.
2006-08-04
Proximity to crops and residential exposure to agricultural herbicides in iowa.
2006-06
Spatial and geographical variations of urban, suburban and rural atmospheric concentrations of phenols and nitrophenols.
2006-03
Herbicide binding and thermal stability of photosystem II isolated from Thermosynechococcus elongatus.
2006-02
Detection of thyroid system-disrupting chemicals using in vitro and in vivo screening assays in Xenopus laevis.
2005-12
Characteristics of 3,5,3'-triiodothyronine (T3)-uptake system of tadpole red blood cells: effect of endocrine-disrupting chemicals on cellular T3 response.
2004-12
Bioaccumulation and toxicity of sediment associated herbicides (ioxynil, pendimethalin, and bentazone) in Lumbriculus variegatus (Oligochaeta) and Chironomus riparius (Insecta).
2003-11
The effect of endocrine disrupting chemicals on thyroid hormone binding to Japanese quail transthyretin and thyroid hormone receptor.
2003-10-15
Off-line solid-phase microextraction and capillary electrophoresis mass spectrometry to determine acidic pesticides in fruits.
2003-02-01
Endocrine disrupting chemicals: interference of thyroid hormone binding to transthyretins and to thyroid hormone receptors.
2003-01-31
Movement of pendimethalin, ioxynil and soil particles to field drainage tiles.
2003-01
The effects of endocrine-disrupting chemicals on thyroid hormone binding to Xenopus laevis transthyretin and thyroid hormone receptor.
2002-12
Analysis of acidic pesticides using in situ derivatization with alkylchloroformate and solid-phase microextraction (SPME) for GC-MS.
2001-09
Patents
Name Type Language
3,5-DIIODO-4-HYDROXYBENZONITRILE SODIUM SALT
Preferred Name English
IOXYNIL-SODIUM
ISO  
Common Name English
IOXYNIL SODIUM [MI]
Common Name English
BENZONITRILE, 4-HYDROXY-3,5-DIIODO-, SODIUM SALT (1:1)
Systematic Name English
IOXYNIL-SODIUM [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 353300
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
Code System Code Type Description
PUBCHEM
23666695
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
ECHA (EC/EINECS)
220-995-7
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
ALANWOOD
ioxynil-sodium
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
FDA UNII
YJ5PH80ES6
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
MERCK INDEX
m11756
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
CAS
2961-62-8
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID0058354
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY