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iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
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ChEBI
> Main
CHEBI:133457 - (3
E
)-3-nonen-2-one
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ChEBI Name
(3
E
)-3-nonen-2-one
ChEBI ID
CHEBI:133457
ChEBI ASCII Name
(3E)-3-nonen-2-one
Definition
An enone that is (
E
)-3-nonene in which the two methylene hydrogens at position 2 have been replaced by an oxo group.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
AnneNiknejad
Supplier Information
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Formula
C9H16O
Net Charge
0
Average Mass
140.223
Monoisotopic Mass
140.12012
InChI
InChI=1S/C9H16O/c1-3-4-5-6-7-8-9(2)10/h7-8H,3-6H2,1-2H3/b8-7+
InChIKey
HDKLIZDXVUCLHQ-BQYQJAHWSA-N
SMILES
CCCCC/C=C/C(C)=O
Roles Classification
Biological Role
(s):
EC 2.5.1.18 (glutathione transferase) inhibitor
An EC 2.5.1.* (non-methyl-alkyl or aryl transferase) inhibitor that interferes with the action of a glutathione transferase (EC 2.5.1.18).
Application
(s):
fumigant
A volatile or volatilizable chemical compound utilized for control of pests in buildings, soil, grain, as well as during processing of goods to be imported or exported to prevent transfer of exotic organisms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(3
E
)-3-nonen-2-one (
CHEBI:133457
)
has role
EC 2.5.1.18 (glutathione transferase) inhibitor (
CHEBI:76797
)
(3
E
)-3-nonen-2-one (
CHEBI:133457
)
has role
fumigant (
CHEBI:39276
)
(3
E
)-3-nonen-2-one (
CHEBI:133457
)
is a
enone (
CHEBI:51689
)
IUPAC Name
(3
E
)-non-3-en-2-one
Synonyms
Sources
(3
E
)-nonen-2-one
UniProt
(
E
)-3-nonen-2-one
ChEBI
(
E
)-non-3-en-2-one
ChEBI
3-Nonen-2-one
ChemIDplus
trans-3-Nonen-2-one
ChemIDplus
Manual Xrefs
Databases
CPD-16995
MetaCyc
LMFA12000133
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
1700427
Reaxys Registry Number
Reaxys
18402-83-0
CAS Registry Number
NIST Chemistry WebBook
18402-83-0
CAS Registry Number
ChemIDplus
Citations
Types
Sources
17245784
PubMed citation
Europe PMC
25619643
PubMed citation
Europe PMC
8142457
PubMed citation
Europe PMC
IND20620571
Agricola citation
Europe PMC
IND21636698
Agricola citation
Europe PMC
Last Modified
31 August 2020