CHEBI:82220 - atraton

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ChEBI Name atraton
ChEBI ID CHEBI:82220
Definition A diamino-1,3,5-triazine that is N-ethyl-N'-(propan-2-yl)-1,3,5-triazine-2,4-diamine substituted by a methoxy group at position 6. It is an agrochemical used as a herbicide.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C9H17N5O
Net Charge 0
Average Mass 211.26420
Monoisotopic Mass 211.14331
InChI InChI=1S/C9H17N5O/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)
InChIKey PXWUKZGIHQRDHL-UHFFFAOYSA-N
SMILES CCNc1nc(NC(C)C)nc(OC)n1
Roles Classification
Chemical Role(s): environmental contaminant
Any minor or unwanted substance introduced into the environment that can have undesired effects.
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): 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): 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 atraton (CHEBI:82220) has role agrochemical (CHEBI:33286)
atraton (CHEBI:82220) has role environmental contaminant (CHEBI:78298)
atraton (CHEBI:82220) has role herbicide (CHEBI:24527)
atraton (CHEBI:82220) has role xenobiotic (CHEBI:35703)
atraton (CHEBI:82220) is a diamino-1,3,5-triazine (CHEBI:38170)
atraton (CHEBI:82220) is a methoxy-1,3,5-triazine (CHEBI:38177)
IUPAC Name
N-ethyl-6-methoxy-N'-(propan-2-yl)-1,3,5-triazine-2,4-diamine
Synonyms Sources
2-Methoxy-4-ethylamino-6-isopropylamino-s-triazine ChemIDplus
2-Methoxy-4-isopropylamino-6-ethylamino-s-triazine ChemIDplus
Manual Xrefs Databases
1692 PPDB
atraton Alan Wood's Pesticides
C19098 KEGG COMPOUND
WO2008062557 Patent
View more database links
Registry Numbers Types Sources
1610-17-9 CAS Registry Number ChemIDplus
1610-17-9 CAS Registry Number NIST Chemistry WebBook
613098 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
21254126 PubMed citation Europe PMC
25301341 PubMed citation Europe PMC
Last Modified
17 November 2014