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Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation

[Image: see text] NOD1 (nucleotide-binding oligomerization domain 1) protein is a member of the NLR (NACHT and leucine rich repeat domain containing proteins) protein family, which plays a key role in innate immunity as a sensor of specific microbial components derived from bacterial peptidoglycans...

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Detalles Bibliográficos
Autores principales: Khan, Pasha M., Correa, Ricardo G., Divlianska, Daniela B., Peddibhotla, Satyamaheshwar, Sessions, E. Hampton, Magnuson, Gavin, Brown, Brock, Suyama, Eigo, Yuan, Hongbin, Mangravita-Novo, Arianna, Vicchiarelli, Michael, Su, Ying, Vasile, Stefan, Smith, Layton H., Diaz, Paul W., Reed, John C., Roth, Gregory P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2011
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3193285/
https://www.ncbi.nlm.nih.gov/pubmed/22003428
http://dx.doi.org/10.1021/ml200158b
Descripción
Sumario:[Image: see text] NOD1 (nucleotide-binding oligomerization domain 1) protein is a member of the NLR (NACHT and leucine rich repeat domain containing proteins) protein family, which plays a key role in innate immunity as a sensor of specific microbial components derived from bacterial peptidoglycans and induction of inflammatory responses. Mutations in NOD proteins have been associated with various inflammatory diseases that affect NF-κB (nuclear factor κB) activity, a major signaling pathway involved in apoptosis, inflammation, and immune response. A luciferase-based reporter gene assay was utilized in a high-throughput screening program conducted under the NIH-sponsored Molecular Libraries Probe Production Center Network program to identify the active scaffolds. Herein, we report the chemical synthesis, structure–activity relationship studies, downstream counterscreens, secondary assay data, and pharmacological profiling of the 2-aminobenzimidazole lead (compound 1c, ML130) as a potent and selective inhibitor of NOD1-induced NF-κB activation.