RIPK1 inhibitors: A key to unlocking the potential of necroptosis in drug development

Eur J Med Chem. 2024 Feb 5:265:116123. doi: 10.1016/j.ejmech.2024.116123. Epub 2024 Jan 3.

Abstract

Within the field of medical science, there is a great deal of interest in investigating cell death pathways in the hopes of discovering new drugs. Over the past two decades, pharmacological research has focused on necroptosis, a cell death process that has just been discovered. Receptor-interacting protein kinase 1 (RIPK1), an essential regulator in the cell death receptor signalling pathway, has been shown to be involved in the regulation of important events, including necrosis, inflammation, and apoptosis. Therefore, researching necroptosis inhibitors offers novel ways to treat a variety of disorders that are not well-treated by the therapeutic medications now on the market. The research and medicinal potential of RIPK1 inhibitors, a promising class of drugs, are thoroughly examined in this study. The journey from the discovery of Necrostatin-1 (Nec-1) to the recent advancements in RIPK1 inhibitors is marked by significant progress, highlighting the integration of traditional medicinal chemistry approaches with modern technologies like high-throughput screening and DNA-encoded library technology. This review presents a thorough exploration of the development and therapeutic potential of RIPK1 inhibitors, a promising class of compounds. Simultaneously, this review highlights the complex roles of RIPK1 in various pathological conditions and discusses potential inhibitors discovered through diverse pathways, emphasizing their efficacy against multiple disease models, providing significant guidance for the expansion of knowledge about RIPK1 and its inhibitors to develop more selective, potent, and safe therapeutic agents.

Keywords: Cell death; Degradation; Drug discovery; Necroptosis; RIPK1; RIPK1 inhibitors.

Publication types

  • Review

MeSH terms

  • Apoptosis
  • Drug Development
  • Humans
  • Necroptosis* / drug effects
  • Necrosis / chemically induced
  • Protein Kinase Inhibitors / chemistry
  • Protein Kinase Inhibitors / pharmacology
  • Receptor-Interacting Protein Serine-Threonine Kinases* / antagonists & inhibitors
  • Receptor-Interacting Protein Serine-Threonine Kinases* / metabolism

Substances

  • Receptor-Interacting Protein Serine-Threonine Kinases
  • RIPK1 protein, human
  • Protein Kinase Inhibitors
  • necrostatin-1