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Necroptosis is a regulated caspase-independent form of necrotic cell death that results in an inflammatory phenotype. This process contributes profoundly to the pathophysiology of numerous neurodegenerative, cardiovascular, infectious, malignant, and inflammatory diseases. Receptor-interacting protein kinase 1 (RIPK1), RIPK3, and the mixed lineage kinase domain-like protein (MLKL) pseudokinase have been identified as the key components of necroptosis signaling and are the most promising targets for therapeutic intervention. Here, we review recent developments in the field of small-molecule inhibitors of necroptosis signaling, provide guidelines for their use as chemical probes to study necroptosis, and assess the therapeutic challenges and opportunities of such inhibitors in the treatment of a range of clinical indications.
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Christopher R. Gardner
The University of Melbourne
Katherine A. Davies
The University of Melbourne
Ying Zhang
The University of Melbourne
Journal of Medicinal Chemistry
The University of Melbourne
Walter and Eliza Hall Institute of Medical Research
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Gardner et al. (Mon,) studied this question.
synapsesocial.com/papers/6a0cd68e7240088826c4019f — DOI: https://doi.org/10.1021/acs.jmedchem.2c01621