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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:biotin sulfoxide
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Accession:CHEBI:62193 term browser browse the term
Definition:A sulfoxide that is the S-oxide of biotin.
Synonyms:exact_synonym: 5-[(3aS,4S,6aR)-5-oxido-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoic acid
 related_synonym: Formula=C10H16N2O4S;   InChI=1S/C10H16N2O4S/c13-8(14)4-2-1-3-7-9-6(5-17(7)16)11-10(15)12-9/h6-7,9H,1-5H2,(H,13,14)(H2,11,12,15)/t6-,7-,9-,17?/m0/s1;   InChIKey=KCSKCIQYNAOBNQ-YBSFLMRUSA-N;   SMILES=[H][C@]12CS(=O)[C@@H](CCCCC(O)=O)[C@@]1([H])NC(=O)N2;   biotin S-oxide
 xref: CAS:10406-89-0;   PMID:13174559;   PMID:16248062;   PMID:6460021;   PMID:7722698;   PMID:8683347;   PMID:8919859;   PMID:9038855;   PMID:9329428;   PMID:9349849;   Reaxys:4492830
 cyclic_relationship: is_conjugate_acid_of CHEBI:62046


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Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            biotin sulfoxide 0
              biotin sulfone 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
                                              monocarboxylic acid amide 0
                                                urea 0
                                                  ureas 0
                                                    biotins 0
                                                      biotin sulfoxide 0
                                                        biotin sulfone 0
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