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pubmed-article:21142106pubmed:abstractTextThe 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.lld:pubmed
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pubmed-article:21142106pubmed:articleTitlePipecolic acid derivatives as small-molecule inhibitors of the Legionella MIP protein.lld:pubmed
pubmed-article:21142106pubmed:affiliationInstitute of Pharmacy and Food Chemistry, University of Wu?rzburg, Wu?rzburg, Germany.lld:pubmed
pubmed-article:21142106pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21142106pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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