A Diarylquinoline Drug Active on the ATP Synthase of Mycobacterium tuberculosis
Johnson & Johnson (United States) · Swedish Institute · +2 more institutions
Abstract
The incidence of tuberculosis has been increasing substantially on a worldwide basis over the past decade, but no tuberculosis-specific drugs have been discovered in 40 years. We identified a diarylquinoline, R207910, that potently inhibits both drug-sensitive and drug-resistant Mycobacterium tuberculosis in vitro (minimum inhibitory concentration 0.06 mug/ml). In mice, R207910 exceeded the bactericidal activities of isoniazid and rifampin by at least 1 log unit. Substitution of drugs included in the World Health Organization's first-line tuberculosis treatment regimen (rifampin, isoniazid, and pyrazinamide) with R207910 accelerated bactericidal activity, leading to complete culture conversion after 2 months…
Citation impact
- FWCI
- 28.60
- Percentile
- 100%
- References
- 13
Authors
18- KAKoen AndriesCorresponding
Johnson & Johnson (United States), Swedish Institute, Johnson & Johnson (United Kingdom)
- PVPeter Verhasselt
Johnson & Johnson (United States), Swedish Institute, Johnson & Johnson (United Kingdom)
- JGJérôme Guillemont
Johnson & Johnson (United States), Swedish Institute, Johnson & Johnson (France), Johnson & Johnson (United Kingdom)
- HWHinrich W. H. Göhlmann
Johnson & Johnson (United States), Swedish Institute, Johnson & Johnson (United Kingdom)
- JNJean‐Marc Neefs
Johnson & Johnson (United States), Swedish Institute, Johnson & Johnson (United Kingdom)
Topics & keywords
- Pyrazinamide
- Bedaquiline
- Mycobacterium tuberculosis
- Isoniazid
- Tuberculosis
- Pharmacology
- Rifampicin
- Drug
- Good health and well-being