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NOD1 and NOD2 are pattern recognition receptors that have important roles in innate immune responses. Although their overactivation has been linked to a number of diseases, NOD2 in particular remains a virtually unexploited target in this respect, with only one structural class of antagonist reported. To gain insight into the structure-activity relationships of NOD2 antagonists, a series of novel analogs was designed and synthesized, and then screened for antagonist activity versus NOD2, and counter-screened versus NOD1. Compounds 32 and 38 were identified as potent and moderately selective NOD2 antagonists, and 33 and 42 as dual NOD1/NOD2 antagonists, with balanced activities against both targets in the low micromolar range. These data enable in-depth exploration of their structure-activity relationships and provide deeper understanding of the structural features required for NOD2 antagonism. Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Citation

Samo Guzelj, Martina Gobec, Dunja Urbančič, Irena Mlinarič-Raščan, Emanuela Corsini, Žiga Jakopin. Structural features and functional activities of benzimidazoles as NOD2 antagonists. European journal of medicinal chemistry. 2020 Mar 15;190:112089

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PMID: 32014680

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