CHEBI:133621 - valanimycin

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ChEBI Name valanimycin
ChEBI ID CHEBI:133621
Definition An azoxy compound that is acrylic acid in which the olefinic hydrogen at position 2 has been replaced by an isobutyl-ONN-azoxy group.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Kristian Axelsen
Supplier Information
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Formula C7H12N2O3
Net Charge 0
Average Mass 172.182
Monoisotopic Mass 172.08479
InChI InChI=1S/C7H12N2O3/c1-5(2)4-9(12)8-6(3)7(10)11/h5H,3-4H2,1-2H3,(H,10,11)/b9-8-
InChIKey DTXMRELKPKEPSO-HJWRWDBZSA-N
SMILES CC(C/[N+](=N/C(C(O)=O)=C)/[O-])C
Metabolite of Species Details
Streptomyces viridifaciens (NCBI:txid48665) of strain MG456-hF10 See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing valanimycin (CHEBI:133621) has functional parent acrylic acid (CHEBI:18308)
valanimycin (CHEBI:133621) has role antimicrobial agent (CHEBI:33281)
valanimycin (CHEBI:133621) has role bacterial metabolite (CHEBI:76969)
valanimycin (CHEBI:133621) is a α,β-unsaturated monocarboxylic acid (CHEBI:79020)
valanimycin (CHEBI:133621) is a azoxy compound (CHEBI:37390)
IUPAC Name
2-[(2-methylpropyl)-ONN-azoxy]prop-2-enoic acid
Synonyms Sources
2-(Isobutyl-(ONN)azoxy)acrylic acid ChemIDplus
2-[(2-methylpropyl)-ONN-azoxy]acrylic acid ChEBI
Manual Xref Database
C00017752 KNApSAcK
View more database links
Registry Numbers Types Sources
101961-60-8 CAS Registry Number ChemIDplus
21142834 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
12406225 PubMed citation Europe PMC
12688722 PubMed citation Europe PMC
16857674 PubMed citation Europe PMC
18451033 PubMed citation SUBMITTER
19548668 PubMed citation Europe PMC
19892763 PubMed citation Europe PMC
28060488 PubMed citation Europe PMC
3754251 PubMed citation Europe PMC
Last Modified
20 February 2017