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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:1H-pyrrole
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Accession:CHEBI:19203 term browser browse the term
Definition:A tautomer of pyrrole that has the double bonds at positions 2 and 4.
Synonyms:related_synonym: 1-aza-2,4-cyclopentadiene;   Formula=C4H5N;   InChI=1S/C4H5N/c1-2-4-5-3-1/h1-5H;   InChIKey=KAESVJOAVNADME-UHFFFAOYSA-N;   Pyrrol;   SMILES=c1cc[nH]c1;   divinyleneimine;   divinylenimine;   imidole;   monopyrrole;   pyrrole
 xref: Beilstein:1159;   CAS:109-97-7;   Gmelin:1705;   PMID:1556177;   PMID:2917974
 cyclic_relationship: is_tautomer_of CHEBI:35557;   is_tautomer_of CHEBI:35558

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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      application 0
        NMR chemical shift reference compound 0
          ammonia 0
            organic amino compound 0
              amine 0
                secondary amine 0
                  1H-pyrrole 0
                    1H-pyrrolediyl group + 0
                    maleimide + 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
                    main group molecular entity 0
                      s-block molecular entity 0
                        hydrogen molecular entity 0
                          hydrides 0
                            inorganic hydride 0
                              pnictogen hydride 0
                                nitrogen hydride 0
                                  azane 0
                                    ammonia 0
                                      organic amino compound 0
                                        amine 0
                                          secondary amine 0
                                            1H-pyrrole 0
                                              1H-pyrrolediyl group + 0
                                              maleimide + 0
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