CHEBI:31739 - josamycin

ChEBI IDCHEBI:31739
ChEBI Namejosamycin
Stars
DefinitionA macrolide antibiotic produced by certain strains of Streptomyces narbonensis var. josamyceticus.
Last Modified22 February 2017
DownloadsMolfile
FormulaC42H69NO15
Net Charge0
Average Mass828.006
Monoisotopic Mass827.46672
SMILESCO[C@@H]1[C@@H](O[C@@H]2O[C@H](C)[C@@H](O[C@H]3C[C@@](C)(O)[C@@H](OC(=O)CC(C)C)[C@H](C)O3)[C@H](N(C)C)[C@H]2O)[C@@H](CC=O)C[C@@H](C)[C@@H](O)/C=C/C=C/C[C@@H](C)OC(=O)C[C@H]1OC(C)=O
InChIInChI=1S/C42H69NO15/c1-23(2)19-32(47)56-40-27(6)53-34(22-42(40,8)50)57-37-26(5)54-41(36(49)35(37)43(9)10)58-38-29(17-18-44)20-24(3)30(46)16-14-12-13-15-25(4)52-33(48)21-31(39(38)51-11)55-28(7)45/h12-14,16,18,23-27,29-31,34-41,46,49-50H,15,17,19-22H2,1-11H3/b13-12+,16-14+/t24-,25-,26-,27+,29+,30+,31-,34+,35-,36-,37-,38+,39+,40+,41+,42-/m1/s1
InChIKeyXJSFLOJWULLJQS-NGVXBBESSA-N
Wikipedia
Roles Classification
Chemical Role:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
antibacterial drug  A drug used to treat or prevent bacterial infections.
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.
Application:
antibacterial drug  A drug used to treat or prevent bacterial infections.
ChEBI Ontology
Outgoing Relation(s)
josamycin (CHEBI:31739) has role antibacterial drug (CHEBI:36047)
josamycin (CHEBI:31739) has role metabolite (CHEBI:25212)
josamycin (CHEBI:31739) is a acetate ester (CHEBI:47622)
josamycin (CHEBI:31739) is a aldehyde (CHEBI:17478)
josamycin (CHEBI:31739) is a disaccharide derivative (CHEBI:63353)
josamycin (CHEBI:31739) is a glycoside (CHEBI:24400)
josamycin (CHEBI:31739) is a macrolide antibiotic (CHEBI:25105)
josamycin (CHEBI:31739) is a tertiary alcohol (CHEBI:26878)
josamycin (CHEBI:31739) is a tertiary amino compound (CHEBI:50996)
INNs  Source
josamycinChemIDplus
josamicinaChemIDplus
josamycinumChemIDplus
josamycineChemIDplus
Synonyms  Source
turimycin A5ChemIDplus
leucomycin V 3-acetate 4B-(3-methylbutanoate)ChemIDplus
Yl-704 A3ChemIDplus
leucomycin V 3-acetate 4β-(3-methylbutanoate)ChemIDplus
leucomycin A3ChemIDplus
leucomycin V 3-acetate 4B-(3-methylbutanoate)ChemIDplus
Manual XrefsDatabases
C12662KEGG COMPOUND
DB01321DrugBank
D01235KEGG DRUG
JOSPDBeChem
JosamycinWikipedia
HMDB0015418HMDB
C00018736KNApSAcK
1518DrugCentral
Registry NumbersSources
CAS:16846-24-5KEGG COMPOUND
Citations