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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 V
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Accession:CHEBI:70213 term browser browse the term
Definition:A beta-carboline alkaloid isolated from Stellaria dichotoma var. lanceolata.
Synonyms:exact_synonym: methyl (2Z)-3-{[(1-acetyl-8-hydroxy-9H-beta-carbolin-3-yl)carbonyl]amino}prop-2-enoate
 related_synonym: Formula=C18H15N3O5;   InChI=1S/C18H15N3O5/c1-9(22)15-17-11(10-4-3-5-13(23)16(10)21-17)8-12(20-15)18(25)19-7-6-14(24)26-2/h3-8,21,23H,1-2H3,(H,19,25)/b7-6-;   InChIKey=MSIFARBJMGDQFS-SREVYHEPSA-N;   SMILES=COC(=O)\\C=C/NC(=O)c1cc2c3cccc(O)c3[nH]c2c(n1)C(C)=O
 xref: PMID:21090796;   Reaxys:21155696

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Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      application 0
        fuel 0
          methanol 0
            methyl ester 0
              dichotomide V 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
                                  carbon oxoacid 0
                                    carboxylic acid 0
                                      carboacyl group 0
                                        univalent carboacyl group 0
                                          carbamoyl group 0
                                            carboxamide 0
                                              secondary carboxamide 0
                                                dichotomide V 0
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