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Development of teixobactin analogues containing hydrophobic, non-proteogenic amino acids that are highly potent against multidrug-resistant bacteria and biofilms
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- Journal Article
- A1
- open access
5-Hydroxy-pyrrolone based building blocks as maleimide alternatives for protein bioconjugation and single-site multi-functionalization
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Teixobactins : a new class of 21st century antibiotics to combat multidrug-resistant bacterial pathogens
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- Journal Article
- A1
- open access
Cysteines and disulfide-bridged macrocyclic mimics of teixobactin analogues and their antibacterial activity evaluation against methicillin-resistant Staphylococcus aureus (MRSA)
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Reviving old protecting group chemistry for site-selective peptide-protein conjugation
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Design and syntheses of highly potent teixobactin analogues against Staphylococcus aureus, methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Enterococci (VRE) in vitro and in vivo
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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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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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Defining the molecular structure of teixobactin analogues and understanding their role in antibacterial activities
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DNA recognition and antimicrobial compounds : exploring the versatility of peptides
(2016)