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Details

Stereochemistry ACHIRAL
Molecular Formula C15H16N4O5S
Molecular Weight 364.376
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFOMETURON-METHYL

SMILES

COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC2=NC(C)=CC(C)=N2

InChI

InChIKey=ZDXMLEQEMNLCQG-UHFFFAOYSA-N
InChI=1S/C15H16N4O5S/c1-9-8-10(2)17-14(16-9)18-15(21)19-25(22,23)12-7-5-4-6-11(12)13(20)24-3/h4-8H,1-3H3,(H2,16,17,18,19,21)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Sulfonylureas have antifungal activity and are potent inhibitors of Candida albicans acetohydroxyacid synthase.
2013-01-10
Predicting the pathway involved in post-translational modification of elongation factor P in a subset of bacterial species.
2010-01-13
A kinetic platform for in silico modeling of the metabolic dynamics in Escherichia coli.
2010
The study of the interactions between heavy metals with sulfonylurea herbicides using ACE.
2009-02
MFS transportome of the human pathogenic yeast Candida albicans.
2008-12-03
Effects of low concentrations of herbicides on full-season, field-grown potatoes.
2008-10-25
Can artificial soil be used in the vegetative vigor test for U.S. pesticide registration?
2008-10
Inference of protein complex activities from chemical-genetic profile and its applications: predicting drug-target pathways.
2008-08-29
An enzyme-centric approach for modelling non-linear biological complexity.
2008-08-01
Transcription factor control of growth rate dependent genes in Saccharomyces cerevisiae: a three factor design.
2008-07-18
Identification of molecular pathways affected by pterostilbene, a natural dimethylether analog of resveratrol.
2008-03-20
Selecting and evaluating native plants for region-specific phytotoxicity testing.
2008-01
Identification of the catalytic subunit of acetohydroxyacid synthase in Haemophilus influenzae and its potent inhibitors.
2007-10-01
Transcriptional regulation by protein kinase A in Cryptococcus neoformans.
2007-03
Pesticide mixtures, endocrine disruption, and amphibian declines: are we underestimating the impact?
2006-04
Unraveling condition specific gene transcriptional regulatory networks in Saccharomyces cerevisiae.
2006-03-21
Sulfometuron resistance as a genetic marker for yeast populations in wine fermentations.
2005-09-21
Engineering of an oenological Saccharomyces cerevisiae strain with pectinolytic activity and its effect on wine.
2005-07-15
New small-molecule synthetic antimycobacterials.
2005-06
Microarray karyotyping of commercial wine yeast strains reveals shared, as well as unique, genomic signatures.
2005-04-16
Elucidating the specificity of binding of sulfonylurea herbicides to acetohydroxyacid synthase.
2005-02-22
Cryptococcus neoformans Ilv2p confers resistance to sulfometuron methyl and is required for survival at 37 degrees C and in vivo.
2004-05
Discovering modes of action for therapeutic compounds using a genome-wide screen of yeast heterozygotes.
2004-01-09
Integration of chemical-genetic and genetic interaction data links bioactive compounds to cellular target pathways.
2004-01
Molecular cloning of an arabidopsis homologue of GCN2, a protein kinase involved in co-ordinated response to amino acid starvation.
2003-08
Acetohydroxyacid synthase from Mycobacterium avium and its inhibition by sulfonylureas and imidazolinones.
2003-06-26
Trace analysis of sulfonylurea herbicides in water by on-line continuous flow liquid membrane extraction--C18 precolumn liquid chromatography with ultraviolet absorbance detection.
2003-05-02
Environmental fate and impacts of sulfometuron on watersheds in the southern United States.
2003-04-24
Slow-release formulations of sulfometuron incorporated in micelles adsorbed on montmorillonite.
2002-05-08
Sulfometuron incorporation in cationic micelles adsorbed on montmorillonite.
2002-05-08
Stable chloroplast transformation of the unicellular red alga Porphyridium species.
2002-05
Isoleucine starvation caused by sulfometuron methyl in Salmonella typhimurium measured by translational frameshifting.
2002-03
Simultaneous determination of binary mixtures of sulfonylurea herbicides in water by first-derivative photochemically induced spectrofluorimetry.
2002-01-05
Molecular analysis of the acetolactate synthase gene of Chlamydomonas reinhardtii and development of a genetically engineered gene as a dominant selectable marker for genetic transformation.
2002-01
Evolution of herbicide resistance in weeds: initial frequency of target site-based resistance to acetolactate synthase-inhibiting herbicides in Lolium rigidum.
2002-01
Inhibitors of branched-chain amino acid biosynthesis as potential antituberculosis agents.
1998-10
Patents
Name Type Language
OUST
Preferred Name English
SULFOMETURON-METHYL
HSDB   ISO   MI  
Common Name English
SULFOMETURON METHYL ESTER
Common Name English
2-(3-(4,6-DIMETHYLPYRIMIDIN-2-YL)UREIDOSULFONYL)BENZOIC ACID METHYL ESTER
Systematic Name English
SULFOMETURON-METHYL [HSDB]
Common Name English
DPX-5648
Code English
SULFOMETURON-METHYL [ISO]
Common Name English
SULFOMETURON-METHYL [MI]
Common Name English
Code System Code Type Description
PUBCHEM
52997
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID0034936
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY
ALANWOOD
sulfometuron-methyl
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY
HSDB
7732
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY
WIKIPEDIA
Sulfometuron methyl
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
277-780-6
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY
MERCK INDEX
m10357
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY Merck Index
FDA UNII
JLY5D60J1A
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY
CAS
74222-97-2
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY
CHEBI
9348
Created by admin on Mon Mar 31 21:40:34 GMT 2025 , Edited by admin on Mon Mar 31 21:40:34 GMT 2025
PRIMARY