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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:annomontine
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Accession:CHEBI:65409 term browser browse the term
Definition:An alkaloid that is beta-carboline substituted at position C-1 by a 2-aminopyrimidin-4-yl moiety. An antiparasitic agent found in Annona montana and Annona foteida.
Synonyms:exact_synonym: 4-(9H-beta-carbolin-1-yl)pyrimidin-2-amine
 related_synonym: Formula=C15H11N5;   InChI=1S/C15H11N5/c16-15-18-8-6-12(20-15)14-13-10(5-7-17-14)9-3-1-2-4-11(9)19-13/h1-8,19H,(H2,16,18,20);   InChIKey=IUDMZJRPDRCJEB-UHFFFAOYSA-N;   SMILES=Nc1nccc(n1)-c1nccc2c3ccccc3[nH]c12
 xref: CAS:82504-00-5
 xref_mesh: MESH:C508838
 xref: PMID:16499336;   PMID:18098158;   PMID:20449727;   PMID:20890807;   PMID:22113579;   Reaxys:5567152

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Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            annomontine 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
                    main group molecular entity 0
                      s-block molecular entity 0
                        hydrogen molecular entity 0
                          hydrides 0
                            inorganic hydride 0
                              pnictogen hydride 0
                                nitrogen hydride 0
                                  azane 0
                                    ammonia 0
                                      organic amino compound 0
                                        aromatic amine 0
                                          aminopyrimidine 0
                                            pyrimidin-2-amine 0
                                              annomontine 0
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