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YTM-T - Ontology Report - Rat Genome Database

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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:YTM-T
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Accession:CHEBI:87402 term browser browse the term
Definition:A member of the class of pyrroloindoles that is an intermediate in the biosynthesis of yatakemycin by Streptomyces sp. TP-A0356
Synonyms:exact_synonym: S-methyl 5-hydroxy-6-[4-hydroxy-6-(5-hydroxy-6-methoxy-1H-indole-2-carbonyl)-3,6-dihydropyrrolo[3,2-e]indole-2-carbonyl]-4-methoxy-3,6,7,8-tetrahydropyrrolo[3,2-e]indole-2-carbothioate
 related_synonym: Formula=C34H27N5O8S;   InChI=1S/C34H27N5O8S/c1-46-26-12-19-14(9-24(26)40)8-20(35-19)32(43)38-6-4-15-17-10-21(36-27(17)25(41)13-23(15)38)33(44)39-7-5-16-18-11-22(34(45)48-3)37-28(18)31(47-2)30(42)29(16)39/h4,6,8-13,35-37,40-42H,5,7H2,1-3H3;   InChIKey=SGORHDMZLHXJRN-UHFFFAOYSA-N;   SMILES=COc1cc2[nH]c(cc2cc1O)C(=O)n1ccc2c3cc([nH]c3c(O)cc12)C(=O)N1CCc2c1c(O)c(OC)c1[nH]c(cc21)C(=O)SC
 xref: PMID:22612591;   Reaxys:22725943

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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            prokaryotic metabolite 0
              bacterial metabolite 0
                YTM-T 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
                                        indoles 0
                                          hydroxyindoles 0
                                            YTM-T 0
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