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The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at The data is made available under the Creative Commons License (CC 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:bauhinoxepin J
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Accession:CHEBI:65472 term browser browse the term
Definition:A dibenzooxepine that is 10,11-dihydrodibenzo[b,f]oxepine-1,4-dione substituted by a methoxy group at position 2. It is isolated from the root extract of Bauhinia purpurea and exhibits antimalarial, antimycobacterial, antifungal and cytotoxic activities.
Synonyms:exact_synonym: 2-methoxy-10,11-dihydrodibenzo[b,f]oxepine-1,4-dione
 related_synonym: 5,6-dihydro-3-methoxy-1,4-dionedibenz[b,f]oxepin;   Formula=C15H12O4;   InChI=1S/C15H12O4/c1-18-13-8-11(16)15-10(14(13)17)7-6-9-4-2-3-5-12(9)19-15/h2-5,8H,6-7H2,1H3;   InChIKey=LAAFMXBDDPXIKZ-UHFFFAOYSA-N;   SMILES=COC1=CC(=O)C2=C(CCc3ccccc3O2)C1=O
 xref: PMID:17480099;   Reaxys:11175327

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  CHEBI ontology 19860
    role 19832
      biological role 19830
        biochemical role 19538
          metabolite 19525
            bauhinoxepin J 0
Path 2
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  CHEBI ontology 19860
    subatomic particle 19858
      composite particle 19858
        hadron 19858
          baryon 19858
            nucleon 19858
              atomic nucleus 19858
                atom 19858
                  main group element atom 19804
                    p-block element atom 19804
                      carbon group element atom 19745
                        carbon atom 19741
                          organic molecular entity 19741
                            heteroorganic entity 19494
                              organochalcogen compound 19257
                                organooxygen compound 19173
                                  carbonyl compound 18897
                                    ketone 17186
                                      cyclic ketone 15703
                                        quinone 8648
                                          p-quinones 8556
                                            bauhinoxepin J 0
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