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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:5'-ethylthioadenosine
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Accession:CHEBI:74046 term browser browse the term
Definition:A thioadenosine that is adenosine with the hydroxy group at C-5' substituted with an ethylthio (ethylsulfanyl) group.
Synonyms:exact_synonym: 5'-S-ethyl-5'-thioadenosine
 related_synonym: Formula=C12H17N5O3S;   InChI=1S/C12H17N5O3S/c1-2-21-3-6-8(18)9(19)12(20-6)17-5-16-7-10(13)14-4-15-11(7)17/h4-6,8-9,12,18-19H,2-3H2,1H3,(H2,13,14,15)/t6-,8-,9-,12-/m1/s1;   InChIKey=HMXHURAGFHWODC-WOUKDFQISA-N;   S-adenosylethane;   SMILES=CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12
 xref: DrugBank:DB07052;   PDBeChem:3DH;   Reaxys:45581

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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            5'-ethylthioadenosine 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
                                  carbohydrates and carbohydrate derivatives 0
                                    carbohydrate 0
                                      carbohydrate derivative 0
                                        glycosyl compound 0
                                          N-glycosyl compound 0
                                            nucleoside 0
                                              ribonucleoside 0
                                                purine ribonucleoside 0
                                                  purines D-ribonucleoside 0
                                                    adenosine 0
                                                      thioadenosine 0
                                                        5'-ethylthioadenosine 0
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