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Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation
Author(s) -
Pasha M. Khan,
Ricardo G. Correa,
Daniela Divlianska,
Satyamaheshwar Peddibhotla,
E. Hampton Sessions,
Gavin Magnuson,
Brock Brown,
Eigo Suyama,
Hongbin Yuan,
Arianna Mangravita-Novo,
Michael Vicchiarelli,
Ying Su,
Stefan Vasile,
Layton H. Smith,
Paul Diaz,
John C. Reed,
Gregory P. Roth
Publication year - 2011
Publication title -
acs medicinal chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.065
H-Index - 66
ISSN - 1948-5875
DOI - 10.1021/ml200158b
Subject(s) - nod1 , identification (biology) , factor (programming language) , computer science , chemistry , computational biology , biochemistry , biology , programming language , nod2 , receptor , innate immune system , botany
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.

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