Design, synthesis, and anti-Staphylococcus aureus evaluation of quinazolinone-based FabH inhibitors
Multidrug-resistant Staphylococcus aureus sparks global crisis and novel fatty acid synthesis enzyme FabH inhibitors could overcome resistance. Through rational design, we developed a series of quinazolinone-benzodioxin FabH inhibitors. The results showed that some of the newly synthesized compounds...
Сохранить в:
| Главные авторы: | , , , , , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Elsevier
2025-11-01
|
| Серии: | Results in Chemistry |
| Предметы: | |
| Online-ссылка: | http://www.sciencedirect.com/science/article/pii/S2211715625008483 |
| Метки: |
Нет меток, Требуется 1-ая метка записи!
|