Abstract
Selective covalent modification of a targeted protein is a powerful tool in chemical biology and drug discovery, with applications ranging from identification and characterization of proteins and their functions to the development of targeted covalent inhibitors. Most covalent ligands contain an affinity motif and an electrophilic warhead that reacts with a nucleophilic residue of the targeted protein. Because the electrophilic warhead is prone to react and modify off-target nucleophiles, its reactivity should be balanced carefully to maximize target selectivity. Arylfluorosulfates have recently emerged as latent electrophiles for selective labeling of context-specific tyrosine and lysine residues in protein pockets. Here, we review the recent but intense introduction of arylfluorosulfates into the arsenal of available warheads for selective covalent modification of proteins. We highlight the untapped potential of this functional group for use in chemical biology and drug discovery.
| Original language | English |
|---|---|
| Journal | Angewandte Chemie - International Edition |
| Volume | 58 |
| Issue number | 4 |
| Pages (from-to) | 957-966 |
| Number of pages | 10 |
| ISSN | 1433-7851 |
| DOIs | |
| Publication status | Published - 21 Jan 2019 |
Keywords
- covalent inhibitors
- drug design
- electrophilic warheads
- medicinal chemistry
- protein modifications