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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.
Term:cellocidin
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Accession:CHEBI:51763 term browser browse the term
Definition:A 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.
Synonyms:exact_synonym: but-2-ynediamide
 related_synonym: 2-butynediamide;   Acetylendicarbonsaeureamid;   Acetylene dicarboxamide;   Acetylenedicarboxamide;   Acetylenedicarboxylic acid diamide;   Aquamycin;   Formula=C4H4N2O2;   InChI=1S/C4H4N2O2/c5-3(7)1-2-4(6)8/h(H2,5,7)(H2,6,8);   InChIKey=JBTGHKUTYAMZEZ-UHFFFAOYSA-N;   Lenamycin;   Renamycin;   SMILES=NC(=O)C#CC(N)=O
 xref: Beilstein:1756134;   CAS:543-21-5;   KNApSAcK:C00018677;   PMID:13563326;   PMID:13563327;   PMID:4736298;   PMID:711614;   Pesticides:cellocidin;   Reaxys:1756134;   Wikipedia:Cellocidin

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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      application 0
        pesticide 0
          cellocidin 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 0
    subatomic particle 0
      composite particle 0
        hadron 0
          baryon 0
            nucleon 0
              atomic nucleus 0
                atom 0
                  main group element atom 0
                    p-block element atom 0
                      carbon group element atom 0
                        carbon atom 0
                          organic molecular entity 0
                            heteroorganic entity 0
                              organochalcogen compound 0
                                organooxygen compound 0
                                  carbon oxoacid 0
                                    carboxylic acid 0
                                      carboacyl group 0
                                        univalent carboacyl group 0
                                          carbamoyl group 0
                                            carboxamide 0
                                              dicarboxylic acid amide 0
                                                dicarboxylic acid diamide 0
                                                  cellocidin 0
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