Towards a new combination therapy for tuberculosis with next generation benzothiazinones
Abstract The benzothiazinone lead compound, BTZ043, kills Mycobacterium tuberculosis by inhibiting the essential flavo‐enzyme DprE1, decaprenylphosphoryl‐beta‐D‐ribose 2‐epimerase. Here, we synthesized a new series of piperazine‐containing benzothiazinones (PBTZ) and show that, like BTZ043, the prec...
I tiakina i:
| Ngā kaituhi matua: | , , , , , , , , , , , , , , , , |
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| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
Springer Nature
2014-02-01
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| Rangatū: | EMBO Molecular Medicine |
| Ngā marau: | |
| Urunga tuihono: | https://doi.org/10.1002/emmm.201303575 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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