Table 2.
Drugs under Clinical Development.
Drug | Chemical Class | Phase | Mechanism of Action |
---|---|---|---|
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diarylquinoline | Pre-phase 1 | Inhibits ATP synthase and inhibits respiration |
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spectinamide | Pre-phase 1 | Binds to the ribosome and inhibits protein synthesis |
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benzothiazinone | 1 | Forms a covalent adduct with DprE1 and inhibits arabinogalactan synthesis |
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benzothiazinone | 1 | Forms a covalent adduct with DprE1 and inhibits arabinogalactan synthesis |
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azaindole | 1 | Binds to DprE1 and inhibits arabinogalactan synthesis |
OPC-167832* | dihydrocarbostyril | 1 | Binds to DprE1 and inhibits |
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arabinogalactan synthesis | ||
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imidazopyridine | 1/2 | Binds to the QcrB subunit of cytochrome bc1 and inhibits respiration |
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oxazolidinone | 1/2 | Binds to the ribosome and inhibits protein synthesis |
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oxazolidinone | 2 | Binds to the ribosome and inhibits protein synthesis |
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oxazolidinone | 2 | Binds to the ribosome and inhibits protein synthesis |
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ethylenediamine | 2 | Binds to MmpL3 and inhibits cell wall synthesis |
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fluoroquinolone | 2 | Binds to DNA gyrase and inhibits DNA replication |
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nitrothiazole | 2 | Disrupts the membrane potential and pH homeostasis |
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diarylquinoline | 3 | Binds to ATP synthase and inhibits respiration |
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nitroimidazole | 3 | Blocks synthesis of mycolic acids and forms NO |
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nitroimidazole | 3 | Blocks synthesis of mycolic acids and forms NO. |
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riminophenazine | 3 | Reduced by NADH dehydrogenase II and subsequently forms reactive oxygen species |
The general structure of OPC-167832 shown here was taken from the US patent No. US2017/0253576 A1.
More compounds in clinical development can be found at www.newtbdrugs.org