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Defining the molecular structure of teixobactin analogues and understanding their role in antibacterial activities
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Syntheses of potent teixobactin analogues against methicillin-resistant Staphylococcus aureus (MRSA) through the replacement of L-allo-enduracididine with its isosteres
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- Journal Article
- A1
- open access
Teixobactin analogues reveal enduracididine to be non-essential for highly potent antibacterial activity and lipid II binding
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- Journal Article
- A1
- open access
Efficient total syntheses and biological activities of two teixobactin analogues