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J

Jinhu Huang

Nanjing Agricultural University
H指数:20
被引数:1,273

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Dual-targeting amphiphilic lipopeptides combat multidrug-resistant Gram-positive pathogens by inhibiting type I signal peptidase and disrupting bacterial membrane

双靶点两亲性脂肽通过抑制I型信号肽酶和破坏细菌膜来对抗多重耐药革兰氏阳性病原体。

2025-10-080
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Corrigendum to: “Discovery and optimization of tetrahydroacridine derivatives as a novel class of antibiotics against multidrug-resistant gram-positive pathogens by targeting type I signal peptidase and disrupting bacterial membrane” [Eur. J. Med. Chem. ISSN 0223–5234, (283, 2025, 117101]

勘误: “通过靶向I型信号肽酶并破坏细菌膜,发现和优化四氢吲哚啉衍生物作为一类新型的抗多药耐药革兰氏阳性病原体的抗生素” [Eur. J. Med. Chem. ISSN 0223–5234, (283, 2025, 117101]

2025-06-300
PRE
Discovery and optimization of tetrahydroacridine derivatives as a novel class of antibiotics against multidrug-resistant Gram-positive pathogens by targeting type I signal peptidase and disrupting bacterial membrane
2025-02-010
PRE