18361-46-1
Chemical Structure
Leucomycin A4
- CAS No.: 18361-46-1
- Formula:C41H67NO15
- Molecular Weight:813.97
IUPAC Name: (2S,3S,4R,6S)-6-(((2R,3S,4R,5R,6S)-6-(((4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-acetoxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-6-yl)oxy)-4-(dimethylamino)-5-hydroxy-2-methyltetrahydro-2H-pyran-3-yl)oxy)-4-hydroxy-2,4-dimethyltetrahydro-2H-pyran-3-yl butyrate
InChIKey: XVTMRUKLMXPAKO-RXUUKHTDSA-N
SMILES: O[C@H]1/C=C\C=C\C[C@H](OC(C[C@@H](OC(C)=O)[C@H](OC)[C@@H](O[C@H]2[C@H](O)[C@@H](N(C)C)[C@H](O[C@@H]3O[C@@H](C)[C@H](OC(CCC)=O)[C@](C)(O)C3)[C@@H](C)O2)[C@@H](CC=O)C[C@H]1C)=O)C
Biological Activity: Leucomycin A4 is a macrolide antibiotic that can be extracted from S. kitasatoensis. Leucomycin A4 inhibits a variety of bacteria, including S. aureus, B. subtilis, C. diphtheriae, N. gonorrhoeae, and H. influenzae (MICs = 0.15, 1.25, 0.15, 0.6, and 0.15 µg/ml, respectively)[1].
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Leucomycin A4 | Leucomycin A4 is a macrolide antibiotic that can be extracted from S. kitasatoensis. Leucomycin A4 inhibits a variety of bacteria, including S. aureus, B. subtilis, C. diphtheriae, N. gonorrhoeae, and H. influenzae (MICs = 0.15, 1.25, 0.15, 0.6, and 0.15 µg/ml, respectively). | |||||||||||||||||||||
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