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Details

Stereochemistry RACEMIC
Molecular Formula C15H18N3O4.Na
Molecular Weight 327.3109
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Imazamox-Sodium

SMILES

[Na+].COCC1=CC(C([O-])=O)=C(N=C1)C2=NC(=O)C(C)(N2)C(C)C

InChI

InChIKey=LYXJJLQNVOKQBQ-UHFFFAOYSA-M
InChI=1S/C15H19N3O4.Na/c1-8(2)15(3)14(21)17-12(18-15)11-10(13(19)20)5-9(6-16-11)7-22-4;/h5-6,8H,7H2,1-4H3,(H,19,20)(H,17,18,21);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C15H18N3O4
Molecular Weight 304.3211
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Cross resistance to ALS-inhibiting herbicides in Euphorbia heterophylla L. biotypes resistant to imazethapyr.
2003
Evaluation of resistance in Cyperus difformis populations to ALS inhibiting herbicides.
2004
Biomassbed: a biological system to reduce pesticide point contamination at farm level.
2004 May
A comparative risk assessment of genetically engineered, mutagenic, and conventional wheat production systems.
2005 Dec
Does the effect of herbicide pulse exposure on aquatic plants depend on Kow or mode of action?
2005 Feb 10
Imidazolinone-tolerant crops: history, current status and future.
2005 Mar
High-performance liquid chromatographic separation of imidazolinone herbicide enantiomers and their methyl derivatives on polysaccharide-coated chiral stationary phases.
2006 Jun 9
Photochemical degradation of imazamox in aqueous solution: influence of metal ions and anionic species on the ultraviolet photolysis.
2006 May 17
Sorption and predicted mobility of herbicides in Baltic soils.
2007 Aug
Molecular and biochemical characterization of an induced mutation conferring imidazolinone resistance in sunflower.
2008 Dec
Comparative genotoxicity evaluation of imidazolinone herbicides in somatic cells of Drosophila melanogaster.
2008 Jan
Are herbicide-resistant crops the answer to controlling Cuscuta?
2009 Jul
Resistance mechanism to bensulfuron-methyl in biotypes of Scirpus mucronatus L. collected in Chilean rice fields.
2009 May 27
Identification of a hybridization window that facilitates sizeable reductions of pollen-mediated gene flow in spring wheat.
2010 Jun
Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays.
2013 Jun 17
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 19:48:40 GMT 2023
Edited
by admin
on Sat Dec 16 19:48:40 GMT 2023
Record UNII
U3NM8KFD9Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Imazamox-Sodium
Common Name English
3-Pyridinecarboxylic acid, 2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-5-(methoxymethyl)-, sodium salt (1:1)
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID70904420
Created by admin on Sat Dec 16 19:48:40 GMT 2023 , Edited by admin on Sat Dec 16 19:48:40 GMT 2023
PRIMARY
CAS
1226788-26-6
Created by admin on Sat Dec 16 19:48:40 GMT 2023 , Edited by admin on Sat Dec 16 19:48:40 GMT 2023
PRIMARY
PUBCHEM
138394675
Created by admin on Sat Dec 16 19:48:40 GMT 2023 , Edited by admin on Sat Dec 16 19:48:40 GMT 2023
PRIMARY
FDA UNII
U3NM8KFD9Z
Created by admin on Sat Dec 16 19:48:40 GMT 2023 , Edited by admin on Sat Dec 16 19:48:40 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE