CHEBI:82012 - fluometuron

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name fluometuron
ChEBI ID CHEBI:82012
Definition A member of the class of 3-(3,4-substituted-phenyl)-1,1-dimethylureas that is urea in which one of the nitrogens is substituted by a 3-(trifluoromethyl)phenyl group while the other is substituted by two methyl groups. It is a herbicide used for the control of broadleaf weeds and annual grasses in cotton.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB2724915, eMolecules:509860, ZINC000000097471
Download Molfile XML SDF
more structures >>
Wikipedia License
Venlafaxine, sold under the brand name Effexor among others, is an antidepressant medication of the serotonin–norepinephrine reuptake inhibitor (SNRI) class. It is used to treat major depressive disorder, generalized anxiety disorder, panic disorder, and social anxiety disorder. Studies have shown that venlafaxine improves post-traumatic stress disorder (PTSD). It may also be used for chronic neuropathic pain. It is taken orally (swallowed by mouth). It is also available as the salt venlafaxine besylate (venlafaxine benzenesulfonate monohydrate) in an extended-release formulation (Venbysi XR). Common side effects include loss of appetite, constipation, dry mouth, dizziness, sweating, insomnia, drowsiness and sexual problems. Severe side effects include an increased risk of suicide, mania, and serotonin syndrome. Antidepressant withdrawal syndrome may occur if stopped. There are concerns that use during the later part of pregnancy can harm the baby. How it works is not entirely clear, but it seems to be related to the potentiation of the activity of some neurotransmitters in the brain. Venlafaxine was approved for medical use in the United States in 1993. It is available as a generic medication. In 2022, it was the 44th most commonly prescribed medication in the United States, with more than 13 million prescriptions.
Read full article at Wikipedia
Formula C10H11F3N2O
Net Charge 0
Average Mass 232.206
Monoisotopic Mass 232.08235
InChI InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)
InChIKey RZILCCPWPBTYDO-UHFFFAOYSA-N
SMILES CN(C)C(=O)NC1=CC=CC(=C1)C(F)(F)F
Roles Classification
Chemical Role(s): environmental contaminant
Any minor or unwanted substance introduced into the environment that can have undesired effects.
Biological Role(s): photosystem-II inhibitor

xenobiotic
A xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
Application(s): photosystem-II inhibitor

agrochemical
An agrochemical is a substance that is used in agriculture or horticulture.
herbicide
A substance used to destroy plant pests.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing fluometuron (CHEBI:82012) has role agrochemical (CHEBI:33286)
fluometuron (CHEBI:82012) has role environmental contaminant (CHEBI:78298)
fluometuron (CHEBI:82012) has role herbicide (CHEBI:24527)
fluometuron (CHEBI:82012) has role photosystem-II inhibitor (CHEBI:26089)
fluometuron (CHEBI:82012) has role xenobiotic (CHEBI:35703)
fluometuron (CHEBI:82012) is a (trifluoromethyl)benzenes (CHEBI:83565)
fluometuron (CHEBI:82012) is a 3-(3,4-substituted-phenyl)-1,1-dimethylurea (CHEBI:157693)
IUPAC Name
1,1-dimethyl-3-[3-(trifluoromethyl)phenyl]urea
Synonyms Sources
1,1-dimethyl-3-(α,α,α-trifluoro-m-tolyl)urea Alan Wood's Pesticides
C 2059 ChemIDplus
Ciba 2059 ChemIDplus
fluometuron UniProt
herbicide C-2059 ChemIDplus
N,N-dimethyl-N'-[3-(trifluoromethyl)phenyl]urea IUPAC
N-(m-trifluoromethylphenyl)-N',N'-dimethylurea ChemIDplus
N-(meta-trifluoromethylphenyl)-N,N'-dimethylurea ChemIDplus
Brand Names Sources
Cotogard ChemIDplus
Cotoran ChemIDplus
Cottonex ChemIDplus
Higalcoton ChemIDplus
Lanex ChemIDplus
Pakhtaran ChemIDplus
Manual Xrefs Databases
15702 ChemSpider
336 PPDB
C18853 KEGG COMPOUND
CPD-23257 MetaCyc
fluometuron Alan Wood's Pesticides
Fluometuron Wikipedia
View more database links
Registry Numbers Types Sources
2164-17-2 CAS Registry Number NIST Chemistry WebBook
2164-17-2 CAS Registry Number ChemIDplus
2217354 Reaxys Registry Number Reaxys
Citations Types Sources
1384777 PubMed citation Europe PMC
15488576 PubMed citation Europe PMC
15537934 PubMed citation Europe PMC
17165123 PubMed citation Europe PMC
17263484 PubMed citation Europe PMC
17604822 PubMed citation Europe PMC
17760353 PubMed citation Europe PMC
18729373 PubMed citation Europe PMC
19356113 PubMed citation Europe PMC
20545302 PubMed citation Europe PMC
22023336 PubMed citation Europe PMC
32626105 PubMed citation Europe PMC
7571346 PubMed citation Europe PMC
IND21963329 Agricola citation Europe PMC
IND23242470 Agricola citation Europe PMC
IND23259860 Agricola citation Europe PMC
IND23265146 Agricola citation Europe PMC
IND23309858 Agricola citation Europe PMC
IND23328937 Agricola citation Europe PMC
IND43726769 Agricola citation Europe PMC
IND43952632 Agricola citation Europe PMC
IND43960254 Agricola citation Europe PMC
IND44774971 Agricola citation Europe PMC
IND601309267 Agricola citation Europe PMC
IND601309285 Agricola citation Europe PMC
IND601311640 Agricola citation Europe PMC
Last Modified
23 November 2020