josamycin
Sign in to saveAlso known as EN-141, Leucomycin V, 3-acetate 4(sup beta)-(3-methylbutanoate), Antibiotic yl-704 a3, Leucomycin v 3-acetate 4b-(3-methylbutanoate), Leucomycin A3, JM, Leucomycin v 3-acetate 4(beta)-(3-methylbutanoate), Leucomycin V, 3-acetate 4B-(3-methylbutanoate)
Josamycin is a macrolide antibiotic. It was isolated by Hamao Umezawa and his colleagues from strains of Streptomyces narbonensis var. josamyceticus var. nova in 1964.
Research
780 papers- [Josamycin].Nihon Koku Geka Gakkai zasshi · 1971
- Josamycin-induced pedal oedema.BMJ (Clinical research ed.) · 1993
- Josamycin suppresses Prevotella intermedia lipopolysaccharide-induced production of nitric oxide and interleukin-1β in murine macrophages.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2018
- Effects of Josamycin on Scratching Behavior in NC/Nga Mice with Atopic Dermatitis-Like Skin Lesions.Biological & pharmaceutical bulletin · 2021
- γ-Cyclodextrin hydrogel for the sustained release of josamycin for potential ocular application.Drug delivery · 2024
via PubMed
Wikidata facts
- Mass
- 827.466721
Show 6 more facts
- chemical formula
- C₄₂H₆₉NO₁₅
- canonical SMILES
- CC1CC=CC=CC(C(CC(C(C(C(CC(=O)O1)OC(=O)C)OC)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)OC(=O)CC(C)C)(C)O)N(C)C)O)CC=O)C)O
- isomeric SMILES
- C[C@@H]1C/C=C/C=C/[C@@H]([C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)OC(=O)C)OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)OC(=O)CC(C)C)(C)O)N(C)C)O)CC=O)C)O
- World Health Organisation international non-proprietary name
- josamycin
- defined daily dose
- 2
- Commons category
- Josamycin
Sources (6)
via Wikidata · CC0
~3 min read
Article
2 sectionsContents
- Adverse effects
- References
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