MetaADEDB 2.0 @ LMMD
Josamycin
(XJSFLOJWULLJQS-NGVXBBESSA-N)
Structure
SMILES
O=CC[C@H]1C[C@@H](C)[C@@H](O)/C=C/C=C/C[C@H](OC(=O)C[C@H]([C@@H]([C@H]1O[C@@H]1O[C@H](C)[C@H]([C@@H]([C@H]1O)N(C)C)O[C@@H]1O[C@@H](C)[C@@H]([C@](C1)(C)O)OC(=O)CC(C)C)OC)OC(=O)C)C
Type(s)
Investigational
ATC code(s)
J01FA07
Molecular Formula:
C42H69NO15
Molecular Weight:
827.995
Log P:
3.0134
Hydrogen Bond Acceptor:
16
Hydrogen Bond Donor:
3
TPSA:
206.05
CAS Number(s):
11033-18-4; 16846-24-5; 56689-45-3
Synonym(s)
1.
Josamycin
2.
EN-141
3.
Josamycine
4.
Kitasamycin A3
5.
Leucomycin A3
6.
Turimycin A5
7.
Wilprafen
8.
EN 141
9.
EN141
External Link(s)
MeSHD015570
PubChem Compound5282165
ChEBI31739
CHEMBLCHEMBL224436
DrugBankDB01321
DrugCentral1518
KEGGcpd:C12662
dr:D01235
ZINC96006021
Adverse Drug Event(s)
NameNumber of ReportsReference(s)Data Source
1Drug Eruptions11792017CTD
2Urticaria11792017CTD
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