CHEBI:83924 - strobilurin B

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ChEBI Name strobilurin B
ChEBI ID CHEBI:83924
Definition An enoate ester that is the methyl ester of (2E,3Z,5E)-6-(4-chloro-3-methoxyphenyl)-2-(methoxymethylene)-3-methylhexa-3,5-dienoic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
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-bc1 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 (2E,3Z,5E)-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 Waiting for 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