Abstract
Antimicrobial peptides are a rich source of potential antibiotic candidates. The tridecaptins, a family of linear lipo-tridecapeptides, are easily synthesized and show strong activity against Gram-negative bacteria. However, their composition includes several expensive amino acids, such as D/L diaminobutyric acid and Dallo-isoleucine, significantly increasing their cost of synthesis. Herein, we report a series of new tridecaptin derivatives that are much cheaper to synthesize and retain strong activity against multidrug-resistant Gram-negative bacteria.
Original language | English |
---|---|
Pages (from-to) | 484-487 |
Number of pages | 4 |
Journal | Med Chem Commun |
Volume | 10 |
Issue number | 3 |
DOIs | |
Publication status | Published - 12 Mar 2019 |
Fingerprint
Dive into the research topics of 'Tridecaptin-Inspired Antimicrobial Peptides with Activity Against Multidrug-Resistant Gram-Negative Bacteria'. Together they form a unique fingerprint.Student theses
-
Structural and mechanistic studies on antimicrobial peptides that target multi-drug resistant bacteria
Ballantine, R. (Author), Cochrane, S. (Supervisor) & Stevenson, P. (Supervisor), Jul 2021Student thesis: Doctoral Thesis › Doctor of Philosophy
File