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Accession:CHEBI:29665 term browser browse the term
Definition:A macrolide antibiotic that is biosynthesised by Streptomyces venezuelae.
Synonyms:exact_synonym: (3R,5R,6S,7S,9R,11E,13S,14R)-14-ethyl-13-hydroxy-3,5,7,9,13-pentamethyl-2,4,10-trioxooxacyclotetradec-11-en-6-yl 3,4,6-trideoxy-3-(dimethylamino)-beta-D-xylo-hexopyranoside
 related_synonym: Albomycetin;   Amaromycin;   Antibiotic B 62169A;   Formula=C28H47NO8;   InChI=1S/C28H47NO8/c1-10-22-28(7,34)12-11-21(30)15(2)13-16(3)25(18(5)23(31)19(6)26(33)36-22)37-27-24(32)20(29(8)9)14-17(4)35-27/h11-12,15-20,22,24-25,27,32,34H,10,13-14H2,1-9H3/b12-11+/t15-,16+,17-,18+,19-,20+,22-,24-,25+,27+,28+/m1/s1;   InChIKey=UZQBOFAUUTZOQE-VSLWXVDYSA-N;   Picromycin;   SMILES=CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@@H](C)C[C@@H](C)C(=O)\\C=C\\[C@]1(C)O
 xref: CAS:19721-56-3 "ChemIDplus";   CAS:19721-56-3 "KEGG COMPOUND";   KEGG:C11999;   KNApSAcK:C00018659;   LIPID_MAPS_instance:LMPK04000038 "LIPID MAPS";   MetaCyc:CPD-13835;   PMID:10421766 "Europe PMC";   PMID:10713461 "Europe PMC";   PMID:12733905 "Europe PMC";   PMID:14531700 "Europe PMC";   PMID:15530995 "Europe PMC";   PMID:16249083 "Europe PMC";   PMID:16724858 "Europe PMC";   PMID:17168607 "Europe PMC";   PMID:18421418 "Europe PMC";   PMID:22168449 "Europe PMC";   PMID:23866020 "Europe PMC";   PMID:9873687 "Europe PMC";   Patent:US2006234958;   Reaxys:67880 "Reaxys";   Wikipedia:Pikromycin
 cyclic_relationship: is_conjugate_base_of CHEBI:76800

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  CHEBI ontology 0
    role 0
      biological role 0
        antimicrobial agent 0
          macrolide antibiotic 0
            pikromycin 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 group 0
                              organic divalent group 0
                                organodiyl group 0
                                  carbonyl group 0
                                    carbonyl compound 0
                                      carboxylic ester 0
                                        lactone 0
                                          macrocyclic lactone 0
                                            macrolide 0
                                              macrolide antibiotic 0
                                                pikromycin 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.