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[1].
Product Specifications
CAS Number
109539-58-4
UNSPSC
12352005
Target
Antibiotic; Bacterial
Related Pathways
Anti-infection
Field of Research
Infection
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
Molecular Formula
C57H103N11O12
Molecular Weight
1134.49
References & Citations
[1]Radics L, et al. Leucinostatins H and K, two novel peptide antibiotics with tertiary amine-oxide terminal group from Paecilomyces marquandii isolation, structure and biological activity. J Antibiot (Tokyo) . 1987 May;40 (5) :714-6.
Shipping Conditions
Room temperature
Scientific Category
Peptides
Clinical Information
No Development Reported
Frequently Asked Questions
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