Literature DB >> 24707857

Nucleotide-binding oligomerization domain (NOD) inhibitors: a rational approach toward inhibition of NOD signaling pathway.

Žiga Jakopin1.   

Abstract

Dysregulation of nucleotide-binding oligomerization domains 1 and 2 (NOD1 and NOD2) has been implicated in the pathology of various inflammatory disorders, rendering them and their downstream signaling proteins potential therapeutic targets. Selective inhibition of NOD1 and NOD2 signaling could be advantageous in treating many acute and chronic diseases; therefore, harnessing the full potential of NOD inhibitors is a key topic in medicinal chemistry. Although they are among the best studied NOD-like receptors (NLRs), the therapeutic potential of pharmacological modulation of NOD1 and NOD2 is largely unexplored. This review is focused on the scientific progress in the field of NOD inhibitors over the past decade, including the recently reported selective inhibitors of NOD1 and NOD2. In addition, the potential approaches to inhibition of NOD signaling as well as the advantages and disadvantages linked with inhibition of NOD signaling are discussed. Finally, the potential directions for drug discovery are also discussed.

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Year:  2014        PMID: 24707857     DOI: 10.1021/jm401841p

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  15 in total

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Journal:  ACS Med Chem Lett       Date:  2018-09-26       Impact factor: 4.345

Review 3.  The Nucleotide Oligomerization Domain-Like Receptors in Kidney Injury.

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5.  Lack of Both Nucleotide-Binding Oligomerization Domain-Containing Proteins 1 and 2 Primes T Cells for Activation-Induced Cell Death.

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Review 7.  Harnessing the untapped potential of nucleotide-binding oligomerization domain ligands for cancer immunotherapy.

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8.  THP-1 Cells and Pro-inflammatory Cytokine Production: An in Vitro Tool for Functional Characterization of NOD1/NOD2 Antagonists.

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Journal:  Int J Mol Sci       Date:  2019-08-30       Impact factor: 5.923

9.  Synthesis of Conformationally Constrained d-Glu-meso-DAP Analogs as Innate Immune Agonists.

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Review 10.  Emerging Mechanisms of Innate Immunity and Their Translational Potential in Inflammatory Bowel Disease.

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