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Accession:CHEBI:134191 term browser browse the term
Definition:A macrolide antibiotic that is 20-oxotylactone having a beta-D-mycaminosyl residue attached at position 5.
Synonyms:exact_synonym: (4R,5S,6S,7R,9R,11E,13E,15S,16R)-16-ethyl-4-hydroxy-5,9,13,15-tetramethyl-2,10-dioxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl 3,6-dideoxy-3-(dimethylamino)-beta-D-glucopyranoside
 related_synonym: 23-Deoxy-5-O-beta-mycaminosyltylonolide;   23-Deoxy-5-O-mycaminosyltylonolide;   Deepoxycirramycin A1;   Formula=C31H51NO9;   InChI=1S/C31H51NO9/c1-9-25-19(4)14-17(2)10-11-23(34)18(3)15-22(12-13-33)30(20(5)24(35)16-26(36)40-25)41-31-29(38)27(32(7)8)28(37)21(6)39-31/h10-11,13-14,18-22,24-25,27-31,35,37-38H,9,12,15-16H2,1-8H3/b11-10+,17-14+/t18-,19+,20+,21-,22+,24-,25-,27+,28-,29-,30-,31+/m1/s1;   InChIKey=FERSDKADYZRIAA-CQGKBTLCSA-N;   SMILES=[C@@H]1([C@H](C[C@H](C(C=CC(=C[C@@H]([C@H](OC(C[C@H]([C@@H]1C)O)=O)CC)C)C)=O)C)CC=O)O[C@H]2[C@H](O)[C@H]([C@@H]([C@H](O2)C)O)N(C)C
 xref: CAS:50507-46-5 "ChemIDplus";   KEGG:C20760;   MetaCyc:CPD-15945;   PMID:2817858 "Europe PMC";   Patent:US4334019;   Reaxys:6457636 "Reaxys"

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Term Annotations click to browse term
  CHEBI ontology 19662
    role 19606
      biological role 19604
        antimicrobial agent 17154
          macrolide antibiotic 324
            20-oxo-5-O-beta-mycaminosyltylactone 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19662
    subatomic particle 19658
      composite particle 19658
        hadron 19658
          baryon 19658
            nucleon 19658
              atomic nucleus 19658
                atom 19658
                  main group element atom 19539
                    p-block element atom 19539
                      carbon group element atom 19422
                        carbon atom 19414
                          organic molecular entity 19414
                            organic group 18340
                              organic divalent group 18330
                                organodiyl group 18330
                                  carbonyl group 18217
                                    carbonyl compound 18217
                                      carboxylic acid 17921
                                        carboacyl group 16944
                                          univalent carboacyl group 16944
                                            formyl group 7680
                                              aldehyde 7680
                                                20-oxo-5-O-beta-mycaminosyltylactone 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.