化学
细胞内
杀伤力
配体(生物化学)
细菌
受体
分离(统计)
生物物理学
细胞生物学
微生物学
生物化学
遗传学
机器学习
计算机科学
生物
作者
Anming Yang,Junfeng Song,Jingbo Li,Youzhi Li,Silei Bai,Cailing Zhou,Min Wang,Yu Zhou,Kang Wen,Miaomiao Luo,Peiren Chen,Bo Liu,Huan Yang,Yugang Bai,Wing‐Leung Wong,Qingyun Cai,Huangsheng Pu,Yu Qian,Wenhao Hu,Wei Huang,Muyang Wan,Chunhui Zhang,Xinxin Feng
摘要
Addressing the global challenge of bacterial resistance demands innovative approaches, among which multitargeting is a widely used strategy. Current strategies of multitargeting, typically achieved through drug combinations or single agents inherently aiming at multiple targets, face challenges such as stringent pharmacokinetic and pharmacodynamic requirements and cytotoxicity concerns. In this report, we propose a bacterial-specific global disruption approach as a vastly expanded multitargeting strategy that effectively disrupts bacterial subcellular organization. This effect is achieved through a pioneering chemical design of ligand-receptor interaction-induced aggregation of small molecules,
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