Abstract
A key to the development of new antibiotics with increased efficiency can be found in (E)-alkene dipeptide isosteres. Here we report on the incorporation of such a dipeptide isostere into a linear peptide precursor by chemical synthesis in combination with enzymatic cyclisation.
Original language | English |
---|---|
Pages (from-to) | 1000-1003 |
Number of pages | 4 |
Journal | ChemBioChem |
Volume | 5 |
Issue number | 7 |
DOIs | |
State | Published - 5 Jul 2004 |
Externally published | Yes |
Keywords
- Alkene dipeptide isostere
- Antibiotics
- Peptide cyclases
- Peptidomimetics
- Postsynthetic modification