CHEBI:51763 - cellocidin

ChEBI IDCHEBI:51763
ChEBI Namecellocidin
Stars
DefinitionA dicarboxylic acid diamide resulting from the formal condensation of both of the carboxy groups of butynedioic acid with ammonia. An antibacterial agent produced by Streptomyces chibaensis.
Last Modified12 October 2020
SubmitterMarcus Ennis
DownloadsMolfile
FormulaC4H4N2O2
Net Charge0
Average Mass112.088
Monoisotopic Mass112.02728
SMILESNC(=O)C#CC(N)=O
InChIInChI=1S/C4H4N2O2/c5-3(7)1-2-4(6)8/h(H2,5,7)(H2,6,8)
InChIKeyJBTGHKUTYAMZEZ-UHFFFAOYSA-N
Wikipedia
Roles Classification
Biological Roles:
antimicrobial agent  A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
antibacterial agent  A substance (or active part thereof) that kills or slows the growth of bacteria.
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application:
pesticide  Strictly, a substance intended to kill pests. In common usage, any substance used for controlling, preventing, or destroying animal, microbiological or plant pests.
ChEBI Ontology
Outgoing Relation(s)
cellocidin (CHEBI:51763) has functional parent butynedioic acid (CHEBI:30781)
cellocidin (CHEBI:51763) has role antibacterial agent (CHEBI:33282)
cellocidin (CHEBI:51763) has role antimicrobial agent (CHEBI:33281)
cellocidin (CHEBI:51763) has role metabolite (CHEBI:25212)
cellocidin (CHEBI:51763) has role pesticide (CHEBI:25944)
cellocidin (CHEBI:51763) is a dicarboxylic acid diamide (CHEBI:35779)
cellocidin (CHEBI:51763) is a primary carboxamide (CHEBI:140324)
cellocidin (CHEBI:51763) is a ynamide (CHEBI:51752)
IUPAC Name 
but-2-ynediamide
Synonyms  Source
AcetylendicarbonsäureamidChemIDplus
Acetylene dicarboxamideChemIDplus
AcetylenedicarboxamideChemIDplus
Acetylenedicarboxylic acid diamideChemIDplus
AquamycinChemIDplus
LenamycinChemIDplus
Manual XrefsDatabases
cellocidinAlan Wood's Pesticides
C00018677KNApSAcK
CellocidinWikipedia
Registry NumbersSources
Reaxys:1756134Reaxys
CAS:543-21-5ChemIDplus
CAS:543-21-5NIST Chemistry WebBook
Citations