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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:laxiracemosin H
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Accession:CHEBI:69007 term browser browse the term
Definition:A terpene alkaloid with a tirucallane skeleton isolated from Dysoxylum lenticellatum.
Synonyms:exact_synonym: 3-[(5alpha,13alpha,14beta,17alpha)-4,4,14-trimethyl-3-oxoandrost-7-en-17-yl]-1H-pyrrole-2,5-dione
 related_synonym: Formula=C26H35NO3;   InChI=1S/C26H35NO3/c1-23(2)19-7-6-18-17(24(19,3)11-10-20(23)28)9-13-25(4)16(8-12-26(18,25)5)15-14-21(29)27-22(15)30/h6,14,16-17,19H,7-13H2,1-5H3,(H,27,29,30)/t16-,17-,19-,24+,25-,26+/m0/s1;   InChIKey=MBOKEBRRTSUMOO-CVRFEKSNSA-N;   SMILES=C[C@@]12CC[C@H]3C(=CC[C@H]4C(C)(C)C(=O)CC[C@]34C)[C@@]1(C)CC[C@H]2C1=CC(=O)NC1=O
 xref: PMID:21954912;   Reaxys:22781646

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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            laxiracemosin H 0
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  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
                                    dicarboxylic acids and O-substituted derivatives 0
                                      dicarboxylic acid 0
                                        C4-dicarboxylic acid 0
                                          butenedioic acid 0
                                            maleic acid 0
                                              maleimides 0
                                                laxiracemosin H 0
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