CHEBI:29491 - 5-O-β-D-mycaminosyltylactone

ChEBI IDCHEBI:29491
ChEBI Name5-O-β-D-mycaminosyltylactone
Stars
ASCII Name5-O-beta-D-mycaminosyltylactone
DefinitionA macrolide antibiotic that is tylactone having a β-D-mycaminosyl residue attached at position 5.
Last Modified13 June 2017
DownloadsMolfile
FormulaC31H53NO8
Net Charge0
Average Mass567.764
Monoisotopic Mass567.37712
SMILESCC[C@H]1C[C@@H](C)C(=O)/C=C/C(C)=C/[C@H](C)[C@@H](CC)OC(=O)C[C@@H](O)[C@H](C)[C@H]1O[C@@H]1O[C@H](C)[C@@H](O)[C@H](N(C)C)[C@H]1O
InChIInChI=1S/C31H53NO8/c1-10-22-15-18(4)23(33)13-12-17(3)14-19(5)25(11-2)39-26(35)16-24(34)20(6)30(22)40-31-29(37)27(32(8)9)28(36)21(7)38-31/h12-14,18-22,24-25,27-31,34,36-37H,10-11,15-16H2,1-9H3/b13-12+,17-14+/t18-,19+,20+,21-,22+,24-,25-,27+,28-,29-,30-,31+/m1/s1
InChIKeyBMKVJAXXBOWJEE-BPFVPZITSA-N
Roles Classification
Biological Roles:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
antimicrobial agent  A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
ChEBI Ontology
Outgoing Relation(s)
5-O-β-D-mycaminosyltylactone (CHEBI:29491) has functional parent tylactone (CHEBI:29700)
5-O-β-D-mycaminosyltylactone (CHEBI:29491) has role metabolite (CHEBI:25212)
5-O-β-D-mycaminosyltylactone (CHEBI:29491) is a enone (CHEBI:51689)
5-O-β-D-mycaminosyltylactone (CHEBI:29491) is a macrolide antibiotic (CHEBI:25105)
5-O-β-D-mycaminosyltylactone (CHEBI:29491) is a monosaccharide derivative (CHEBI:63367)
5-O-β-D-mycaminosyltylactone (CHEBI:29491) is conjugate base of 5-O-β-D-mycaminosyltylactone(1+) (CHEBI:76802)
Incoming Relation(s)
5-O-β-D-mycaminosyltylactone(1+) (CHEBI:76802) is conjugate acid of 5-O-β-D-mycaminosyltylactone (CHEBI:29491)
IUPAC Name 
(4R,5S,6S,7S,9R,11E,13E,15S,16R)-7,16-diethyl-4-hydroxy-5,9,13,15-tetramethyl-2,10-dioxooxacyclohexadeca-11,13-dien-6-yl 3,6-dideoxy-3-(dimethylamino)-β-D-glucopyranoside
Synonyms  Source
5-O-beta-D-MycaminosyltylactoneKEGG COMPOUND
20-deoxo-23-deoxy-5-O-(3,6-dideoxy-3-(dimethylamino)-beta-D-glucopyranosyl)-tylonolideChemIDplus
5-McptChemIDplus
5-O-MycaminosylprotylonolideChemIDplus
Manual XrefsDatabases
C12001KEGG COMPOUND
WO2005054265Patent
Registry NumbersSources
Reaxys:6454572Reaxys
CAS:81661-90-7ChemIDplus
Citations