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> Main
CHEBI:83924 - strobilurin B
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ChEBI Ontology
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ChEBI Name
strobilurin B
ChEBI ID
CHEBI:83924
Definition
An enoate ester that is the methyl ester of (2
E
,3
Z
,5
E
)-6-(4-chloro-3-methoxyphenyl)-2-(methoxymethylene)-3-methylhexa-3,5-dienoic acid.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C17H19ClO4
Net Charge
0
Average Mass
322.78300
Monoisotopic Mass
322.09719
InChI
InChI=1S/C17H19ClO4/c1-
12(14(11-
20-
2)
17(19)
22-
4)
6-
5-
7-
13-
8-
9-
15(18)
16(10-
13)
21-
3/h5-
11H,1-
4H3/b7-
5+,12-
6-
,14-
11+
InChIKey
ZDIQYKMDNQULMX-PJUQCDRASA-N
SMILES
CO\C=C(/C(/C)=C\C=C\c1ccc(Cl)c(OC)c1)\C(=O)OC
Metabolite of Species
Details
Favolaschia tonkinensis
(NCBI:txid333979)
See:
PubMed
Strobilurus tenacellus
(NCBI:txid41251)
of strain No.21602 See:
PubMed
Roles Classification
Biological Role
(s):
antifungal agent
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
(via
methoxyacrylate strobilurin antifungal agent
)
(via
strobilurin antifungal agent
)
(via
antibiotic antifungal agent
)
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
mitochondrial cytochrome-bc1 complex inhibitor
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
strobilurin B (
CHEBI:83924
)
has role
antifungal agent (
CHEBI:35718
)
strobilurin B (
CHEBI:83924
)
has role
fungal metabolite (
CHEBI:76946
)
strobilurin B (
CHEBI:83924
)
has role
mitochondrial cytochrome-
b
c
1
complex inhibitor (
CHEBI:38499
)
strobilurin B (
CHEBI:83924
)
is a
enoate ester (
CHEBI:51702
)
strobilurin B (
CHEBI:83924
)
is a
enol ether (
CHEBI:47985
)
strobilurin B (
CHEBI:83924
)
is a
methoxyacrylate strobilurin antifungal agent (
CHEBI:86484
)
strobilurin B (
CHEBI:83924
)
is a
monochlorobenzenes (
CHEBI:83403
)
strobilurin B (
CHEBI:83924
)
is a
monomethoxybenzene (
CHEBI:25235
)
IUPAC Name
methyl (2
E
,3
Z
,5
E
)-
6-
(4-
chloro-
3-
methoxyphenyl)-
2-
(methoxymethylene)-
3-
methylhexa-
3,5-
dienoate
Manual Xref
Database
C00018155
KNApSAcK
View more database links
Registry Numbers
Types
Sources
5285030
Reaxys Registry Number
Reaxys
65105-52-4
CAS Registry Number
ChemIDplus
Citations
Types
Sources
11561403
PubMed citation
Europe PMC
16493822
PubMed citation
Europe PMC
17474024
PubMed citation
Europe PMC
20329738
PubMed citation
Europe PMC
563391
PubMed citation
Europe PMC
6271595
PubMed citation
Europe PMC
Last Modified
15 July 2015