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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:gliotoxin
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Accession:CHEBI:5385 term browser browse the term
Definition:A pyrazinoindole with a disulfide bridge spanning a dioxo-substituted pyrazine ring; mycotoxin produced by several species of fungi.
Synonyms:exact_synonym: (3R,5aS,6S,10aR)-6-hydroxy-3-(hydroxymethyl)-2-methyl-2,3,6,10-tetrahydro-5aH-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione
 related_synonym: Aspergillin;   Formula=C13H14N2O4S2;   InChI=1S/C13H14N2O4S2/c1-14-10(18)12-5-7-3-2-4-8(17)9(7)15(12)11(19)13(14,6-16)21-20-12/h2-4,8-9,16-17H,5-6H2,1H3/t8-,9-,12+,13+/m0/s1;   InChIKey=FIVPIPIDMRVLAY-RBJBARPLSA-N;   SMILES=[H][C@@]12[C@@H](O)C=CC=C1C[C@@]13SS[C@@](CO)(N(C)C1=O)C(=O)N23
 xref: Beilstein:50675;   CAS:67-99-2;   KEGG:C10595;   KNApSAcK:C00002340
 xref_mesh: MESH:D005912
 xref: PMID:16020669;   PMID:23832115;   PMID:24368570;   PMID:24847038;   PMID:25062268;   PMID:25494483;   PMID:25766143;   PMID:25816130;   PMID:25982450;   PPDB:2793;   Reaxys:50675;   Wikipedia:Gliotoxin


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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        immunomodulator 0
          immunosuppressive agent 0
            gliotoxin 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
                                              peptide 0
                                                oligopeptide 0
                                                  dipeptide 0
                                                    gliotoxin 0
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