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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:G-Indomycinone
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Accession:CHEBI:219879 term browser browse the term
Synonyms:exact_synonym: 11-hydroxy-2-(2-hydroxybutan-2-yl)-5-methylnaphtho[2,3-h]chromene-4,7,12-trione
 related_synonym: Formula=C22H18O6;   InChI=1S/C22H18O6/c1-4-22(3,27)15-9-14(24)16-10(2)8-12-18(21(16)28-15)20(26)17-11(19(12)25)6-5-7-13(17)23/h5-9,23,27H,4H2,1-3H3/t22-/m0/s1;   InChIKey=SUGGWZIKECZBID-QFIPXVFZSA-N;   SMILES=O=C1C2=C3OC(=CC(C3=C(C)C=C2C(=O)C=4C1=C(O)C=CC4)=O)[C@@](O)(CC)C
 xref: Chemspider:10352882


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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    chemical entity 0
      molecular entity 0
        polyatomic entity 0
          molecule 0
            cyclic compound 0
              homocyclic compound 0
                carbocyclic compound 0
                  carbopolycyclic compound 0
                    carbotricyclic compound 0
                      anthracenes 0
                        anthraquinone 0
                          G-Indomycinone 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
                                  carbonyl compound 0
                                    ketone 0
                                      cyclic ketone 0
                                        quinone 0
                                          acenoquinone 0
                                            anthraquinone 0
                                              G-Indomycinone 0
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