期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 54, 期 1, 页码 277-283出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm101156y
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资金
- Deutsche Forschungsgemeinschaft [SFB 630]
The macrophage infectivity potentiator (MIP) protein is a major virulence factor of Legionella pneumophila, the causative agent of Legionnaires' disease MIP belongs to the FK506-binding proteins (FKBP) and is necessary for optimal intracellular survival and lung tissue dissemination of L pneumophila We aimed to identify new small-molecule inhibitors of MIP by starting from known FKBP12 ligands Computational analysis, synthesis, and biological testing of pipecolic acid derivatives revealed a promising scaffold for new MIP inhibitors
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