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ONTOLOGY REPORT - ANNOTATIONS


Term:5-O-beta-D-mycaminosyl-20-oxotylonolide
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Accession:CHEBI:77009 term browser browse the term
Definition:A macrolide antibiotic that is 20-oxotylactone having a 5-O-beta-D-mycaminosyl residue attached at position 6.
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)oxacyclohexadeca-11,13-dien-6-yl 3,6-dideoxy-3-(dimethylamino)-beta-D-glucopyranoside
 related_synonym: 20-oxo-5-O-beta-D-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=CC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O)[C@@H]([C@H]2O)N(C)C)[C@@H](CC=O)C[C@@H](C)C(=O)\\C=C\\C(C)=C\\[C@@H]1C
 xref: CAS:50507-46-5 "ChemIDplus";   MetaCyc:CPD-15945
 cyclic_relationship: is_conjugate_base_of CHEBI:76803


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  CHEBI ontology 0
    role 0
      biological role 0
        antimicrobial agent 0
          macrolide antibiotic 0
            5-O-beta-D-mycaminosyl-20-oxotylonolide 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 acid 0
                                        carboacyl group 0
                                          univalent carboacyl group 0
                                            formyl group 0
                                              aldehyde 0
                                                5-O-beta-D-mycaminosyl-20-oxotylonolide 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.