CHEBI:82042 - sulfometuron

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ChEBI Name sulfometuron
ChEBI ID CHEBI:82042
Definition An N-sulfonylurea that is urea substituted by 4,6-dimethylpyrimidin-2-yl and (2-carboxyphenyl)sulfonyl groups at positions 1 and 3, respectively.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C14H14N4O5S
Net Charge 0
Average Mass 350.350
Monoisotopic Mass 350.06849
InChI InChI=1S/C14H14N4O5S/c1-8-7-9(2)16-13(15-8)17-14(21)18-24(22,23)11-6-4-3-5-10(11)12(19)20/h3-7H,1-2H3,(H,19,20)(H2,15,16,17,18,21)
InChIKey FZMKKCQHDROFNI-UHFFFAOYSA-N
SMILES CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C2=CC=CC=C2C(O)=O)=N1
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): EC 2.2.1.6 (acetolactate synthase) inhibitor
An EC 2.2.1.* (transketolase/transaldolase) inhibitor that interferes with the action of acetolactate synthase (EC 2.2.1.6).
Application(s): herbicide
A substance used to destroy plant pests.
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ChEBI Ontology
Outgoing sulfometuron (CHEBI:82042) has role EC 2.2.1.6 (acetolactate synthase) inhibitor (CHEBI:22180)
sulfometuron (CHEBI:82042) has role herbicide (CHEBI:24527)
sulfometuron (CHEBI:82042) is a N-sulfonylurea (CHEBI:76983)
sulfometuron (CHEBI:82042) is a benzoic acids (CHEBI:22723)
sulfometuron (CHEBI:82042) is a monocarboxylic acid (CHEBI:25384)
sulfometuron (CHEBI:82042) is a pyrimidines (CHEBI:39447)
Incoming sulfometuron methyl (CHEBI:9348) has functional parent sulfometuron (CHEBI:82042)
IUPAC Name
2-{[(4,6-dimethylpyrimidin-2-yl)carbamoyl]sulfamoyl}benzoic acid
Synonyms Sources
2-(3-(4,6-dimethylpyrimidin-2-yl)ureidosulfonyl)benzoic acid ChemIDplus
2-[3-(4,6-dimethylpyrimidin-2-yl)ureidosulfonyl]benzoic acid ChEBI
2-[[[[(4,6-dimethyl-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]benzoic acid Alan Wood's Pesticides
sulfométuron ChEBI
Manual Xrefs Databases
47882 ChemSpider
C18895 KEGG COMPOUND
sulfometuron Alan Wood's Pesticides
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Registry Numbers Types Sources
74223-56-6 CAS Registry Number ChemIDplus
937935 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11982411 PubMed citation Europe PMC
11982412 PubMed citation Europe PMC
14572103 PubMed citation Europe PMC
16159170 PubMed citation Europe PMC
17325226 PubMed citation Europe PMC
20821425 PubMed citation Europe PMC
20872651 PubMed citation Europe PMC
22383419 PubMed citation Europe PMC
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27976507 PubMed citation Europe PMC
Last Modified
15 October 2021