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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:pinosylvin
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Accession:CHEBI:36011 term browser browse the term
Definition:A stilbenol that has formula C14H12O2.
Synonyms:exact_synonym: 5-(2-phenylethenyl)benzene-1,3-diol
 related_synonym: 5-(2-phenylethenyl)-1,3-benzenediol;   5-(2-phenylvinyl)benzene-1,3-diol;   Formula=C14H12O2;   InChI=1S/C14H12O2/c15-13-8-12(9-14(16)10-13)7-6-11-4-2-1-3-5-11/h1-10,15-16H;   InChIKey=YCVPRTHEGLPYPB-UHFFFAOYSA-N;   SMILES=[H]C(=C([H])c1cc(O)cc(O)c1)c1ccccc1
 alt_id: CHEBI:14840;   CHEBI:8226
 xref: Beilstein:2047772;   CAS:102-61-4;   KEGG:C01745;   LINCS:LSM-24964
 xref_mesh: MESH:C049032



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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    chemical entity 0
      atom 0
        nonmetal atom 0
          carbon atom 0
            organic molecular entity 0
              olefinic compound 0
                stilbenoid 0
                  stilbenol 0
                    pinosylvin 0
                      cis-pinosylvin 0
                      trans-pinosylvin 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
                            organic molecule 0
                              organic cyclic compound 0
                                organic aromatic compound 0
                                  stilbenoid 0
                                    stilbenol 0
                                      pinosylvin 0
                                        cis-pinosylvin 0
                                        trans-pinosylvin 0
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