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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:chaetoglobosin V
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Accession:CHEBI:68777 term browser browse the term
Definition:A cytochalasan alkaloid found in Chaetomium globosum.
Synonyms:exact_synonym: (3S,3aR,6S,6aR,7E,10S,10aS,13aS,15aR)-6,12-dihydroxy-3-(1H-indol-3-ylmethyl)-4,5,10,11-tetramethyl-2,3,3a,6,6a,9,10,10a,13a,14-decahydro-1H-cyclopenta[7,8]cyclodeca[1,2-d]isoindole-1,13,15-trione
 related_synonym: Formula=C32H36N2O5;   InChI=1S/C32H36N2O5/c1-15-8-7-10-22-28(36)17(3)16(2)27-24(12-19-14-33-23-11-6-5-9-20(19)23)34-31(39)32(22,27)25(35)13-21-26(15)18(4)29(37)30(21)38/h5-7,9-11,14-15,21-22,24,26-28,33,36-37H,8,12-13H2,1-4H3,(H,34,39)/b10-7+/t15-,21-,22-,24-,26+,27-,28+,32+/m0/s1;   InChIKey=PRTGSLLKDHOTJT-HMPNXLKUSA-N;   SMILES=C[C@H]1C\\C=C\\[C@H]2[C@H](O)C(C)=C(C)[C@H]3[C@H](Cc4c[nH]c5ccccc45)NC(=O)[C@@]23C(=O)C[C@H]2[C@H]1C(C)=C(O)C2=O
 xref: PMID:22593034;   Reaxys:21630862

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  CHEBI ontology 0
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      molecular entity 0
        polyatomic entity 0
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            cyclic compound 0
              macrocycle 0
                chaetoglobosin V 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
                            organic molecule 0
                              organic cyclic compound 0
                                organic heterocyclic compound 0
                                  organic heteropolycyclic compound 0
                                    organic heterobicyclic compound 0
                                      benzopyrrole 0
                                        isoindoles 0
                                          cytochalasin 0
                                            cytochalasan alkaloid 0
                                              chaetoglobosin V 0
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