Abstract
Multi-drug resistant tuberculosis (MDR-TB) is of growing global concern and threatens to undermine increasing efforts to control the worldwide spread of tuberculosis (TB). Bedaquiline has recently emerged as a new drug developed to specifically treat MDR-TB. Despite being highly effective as a result of its unique mode of action, bedaquiline has been associated with significant toxicities and as such, safety concerns are limiting its clinical use. In order to access pharmaceutical agents that exhibit an improved safety profile for the treatment of MDR-TB, new synthetic pathways to facilitate the preparation of bedaquiline and analogues thereof have been discovered.
| Original language | English |
|---|---|
| Pages (from-to) | 9622-9628 |
| Number of pages | 7 |
| Journal | Organic & Biomolecular Chemistry |
| Volume | 14 |
| Issue number | 40 |
| DOIs | |
| Publication status | Published - 28 Oct 2016 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Projects
- 1 Finished
-
Interrogating diarylquinoline toxicity with targeted organic synthesis
Baell, J. (Primary Chief Investigator (PCI)) & Zhang, L. (Partner Investigator (PI))
ARC - Australian Research Council, Monash University
2/01/14 → 31/12/17
Project: Research
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