109539-58-4
Chemical Structure
Leucinostatin H
- CAS No.: 109539-58-4
- Formula:C57H103N11O12
- Molecular Weight:1134.49
IUPAC Name: 6-(1-hydroxy-2-methylpropyl)-3,12,15-triisobutyl-N,N,9,9,18,18,21,21,28-nonamethyl-1-(4-methyl-1-(4-methylhex-2-enoyl)pyrrolidin-2-yl)-1,4,7,10,13,16,19,22,26-nonaoxo-2,5,8,11,14,17,20,23,27-nonaazanonacosan-29-amine oxide
InChIKey: YSPNHJIQHQTTOK-UHFFFAOYSA-N
SMILES: O=C(N[C@H](C[N+](C)(C)[O-])C)CCNC(C(C)(C)NC(C(C)(C)NC([C@H](CC(C)C)NC([C@H](CC(C)C)NC(C(C)(C)NC([C@H]([C@H](O)C(C)C)NC([C@H](CC(C)C)NC([C@@H]1C[C@@H](CN1C(/C=C/[C@@H](C)CC)=O)C)=O)=O)=O)=O)=O)=O)=O)=O
Biological Activity: Leucinostatin H is a polypeptide antibiotic discovered in Paecilomyces marquandii, characterized by a tertiary amine-oxide terminal group. Leucinostatin H exhibits inhibitory activity against Gram-positive bacteria, such as Bacillus subtilis, B. cereus, and Staphylococcus aureus (MIC 10-100 μg/mL). Leucinostatin H holds potential for research in anti-infective and plant disease control applications[1].
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Leucinostatin H | Leucinostatin H is a polypeptide antibiotic discovered in Paecilomyces marquandii, characterized by a tertiary amine-oxide terminal group. Leucinostatin H exhibits inhibitory activity against Gram-positive bacteria, such as Bacillus subtilis, B. cereus, and Staphylococcus aureus (MIC 10-100 μg/mL). Leucinostatin H holds potential for research in anti-infective and plant disease control applications. | |||||||||||||||||||||
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Keywords
