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December 19, 2018Journal of Medicinal Chemistry729 citationsOpen Access

Emerging and Re-Emerging Warheads for Targeted Covalent Inhibitors: Applications in Medicinal Chemistry and Chemical Biology

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MGMatthias GehringerSLStefan Laufer

Key Points

  • To review emerging and re-emerging chemical warheads beyond conventional α,β-unsaturated amides for designing targeted covalent inhibitors.
  • Reviewed literature on novel reactive functional groups used for covalent-reversible and irreversible target engagement.
  • Assessed warhead reactivity profiles and examined case studies across medicinal chemistry and chemical biology targeting cysteine and non-cysteine amino acids.
  • Identified alternative reactive chemistries that expand covalent drug design beyond traditional cysteine-targeting acrylamide scaffolds.
  • Highlighted promising reactive functional groups that can covalently engage noncatalytic cysteine residues and other poorly conserved amino acids.

Abstract

Targeted covalent inhibitors (TCIs) are designed to bind poorly conserved amino acids by means of reactive groups, the so-called warheads. Currently, targeting noncatalytic cysteine residues with acrylamides and other α,β-unsaturated carbonyl compounds is the predominant strategy in TCI development. The recent ascent of covalent drugs has stimulated considerable efforts to characterize alternative warheads for the covalent-reversible and irreversible engagement of noncatalytic cysteine residues as well as other amino acids. This Perspective article provides an overview of warheads-beyond α,β-unsaturated amides-recently used in the design of targeted covalent ligands. Promising reactive groups that have not yet demonstrated their utility in TCI development are also highlighted. Special emphasis is placed on the discussion of reactivity and of case studies illustrating applications in medicinal chemistry and chemical biology.

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Cite This Study

Gehringer et al. (2018) studied this question.

synapsesocial.com/papers/69dab6dc78a3e0e288684132https://doi.org/10.1021/acs.jmedchem.8b01153
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