Abstract
Benzoxaboroles are a new class of leucyl-tRNA synthetase inhibitors. We recently reported that the antitubercular 4-halogenated benzoxaboroles are active against Mycobacterium abscessus. Here, we find that the nonhalogenated benzoxaborole epetraborole, a clinical candidate developed for Gram-negative infections, is also active against M. abscessus in vitro and in a mouse model of infection. This expands the repertoire of advanced lead compounds for the discovery of a benzoxaborole-based candidate to treat M. abscessus lung disease.
| Original language | English |
|---|---|
| Article number | e01156-21 |
| Journal | Antimicrobial Agents and Chemotherapy |
| Volume | 65 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 2021 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Benzoxaborole
- Epetraborole
- Mycobacterium abscessus
- NTM
- Nontuberculous mycobacteria
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