Discovery of NP3-742: A Structurally Diverse NLRP3 Inhibitor Identified through an Unusual Phenol Replacement

NLRP3 is a molecular sensor present in innate immune cells which recognizes a variety of danger signals such as MSU, ATP, or Aβ. Upon activation, it seeds a protein complex termed the inflammasome, which leads to secretion of the proinflammatory cytokines IL-1β and IL-18 and initiates pyroptotic cell death. NLRP3 inflammasome activation has been associated with a wide range of diseases including atherosclerosis, gout, and cancer. In this publication, we describe the replacement of the phenol moiety with indoles in the recently described pyridazine scaffold. This replacement required a shift of the hydrogen bond donor from the "<i>ortho</i>" to the "<i>meta</i>" position, relative to the pyridazine ring. Initial indole analog <b>7</b> demonstrated a robust in vivo IL-1β inhibition, but also a significant hERG inhibition. Decreasing lipophilicity led to the discovery of <b>NP3-742</b>, demonstrating a favorable overall profile including diminished hERG inhibition and in vivo efficacy in a mouse peritonitis model.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-10-15
DOI
https://doi.org/10.1021/acs.jmedchem.5c02412
Citations
1
Primary Topic
Inflammasome and immune disorders
Type
article
Field-Weighted Citation Impact
0.81
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article

Discovery of NP3-742: A Structurally Diverse NLRP3 Inhibitor Identified through an Unusual Phenol Replacement

Rainer Machauer, Christian Fischer, Daniel Pflieger, Angela Mackay et al.
1 citations
Journal of Medicinal Chemistry
Inflammasome and immune disorders
0.81
article

Discovery of NP3-742: A Structurally Diverse NLRP3 Inhibitor Identified through an Unusual Phenol Replacement

Rainer Machauer, Christian Fischer, Daniel Pflieger, Angela Mackay, Juraj Velcicky, Christopher J. Farady, Janet Dawson, Roland Steiner, Nina Gommermann, J. A. Wunderlich, Karen Beltz, Philipp Janser, Daniel R. Smith, Daniela Angst, Eric Vangrevelinghe, Adeline Unterreiner, Aleksandar Stojanović, Celine Dubois, Andreas Heizmann, Joëlle Rubert, Thomas Troxler, Silke Brenneisen, Jean‐Baptiste Langlois, Michael Wright, Christelle Arnold, Honnappa Srinivas, Slavica Ilić, Nicole von Burg, Magdalena Maschlej, Sarah Monnerat, Jacinda Ristov, Günther Schwalm
article en
1 citations

Abstract

NLRP3 is a molecular sensor present in innate immune cells which recognizes a variety of danger signals such as MSU, ATP, or Aβ. Upon activation, it seeds a protein complex termed the inflammasome, which leads to secretion of the proinflammatory cytokines IL-1β and IL-18 and initiates pyroptotic cell death. NLRP3 inflammasome activation has been associated with a wide range of diseases including atherosclerosis, gout, and cancer. In this publication, we describe the replacement of the phenol moiety with indoles in the recently described pyridazine scaffold. This replacement required a shift of the hydrogen bond donor from the "<i>ortho</i>" to the "<i>meta</i>" position, relative to the pyridazine ring. Initial indole analog <b>7</b> demonstrated a robust in vivo IL-1β inhibition, but also a significant hERG inhibition. Decreasing lipophilicity led to the discovery of <b>NP3-742</b>, demonstrating a favorable overall profile including diminished hERG inhibition and in vivo efficacy in a mouse peritonitis model.

Journal of Medicinal ChemistryVol. 68(21)
Novartis (Switzerland) (CH), Novartis (China) (CN)
Openalex Percentile: Top 22%
Inflammasome and immune disorders
0.81
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