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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:dichotomide VI
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Accession:CHEBI:70214 term browser browse the term
Definition:A beta-carboline alkaloid that is 9H-beta-carboline substituted by acetyl group at position 1, a hydroxy group at position 8 and an aminocarbonyl at position 3. It has been isolated from Stellaria dichotoma var. lanceolata.
Synonyms:exact_synonym: 1-acetyl-8-hydroxy-9H-beta-carboline-3-carboxamide
 related_synonym: Formula=C14H11N3O3;   InChI=1S/C14H11N3O3/c1-6(18)11-13-8(5-9(16-11)14(15)20)7-3-2-4-10(19)12(7)17-13/h2-5,17,19H,1H3,(H2,15,20);   InChIKey=BQCOVTPWSCEKDZ-UHFFFAOYSA-N;   SMILES=CC(=O)c1nc(cc2c3cccc(O)c3[nH]c12)C(N)=O
 xref: PMID:21090796

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Term Annotations click to browse term
  CHEBI ontology 2
    role 2
      biological role 2
        biochemical role 2
          metabolite 2
            eukaryotic metabolite 2
              plant metabolite 1
                dichotomide VI 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 2
    subatomic particle 2
      composite particle 2
        hadron 2
          baryon 2
            nucleon 2
              atomic nucleus 2
                atom 2
                  main group element atom 2
                    p-block element atom 2
                      carbon group element atom 2
                        carbon atom 2
                          organic molecular entity 2
                            heteroorganic entity 2
                              organochalcogen compound 1
                                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
                                                dichotomide VI 0
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