Discovery and development of plasma kallikrein inhibitors for multiple diseases

Eur J Med Chem. 2020 Mar 15:190:112137. doi: 10.1016/j.ejmech.2020.112137. Epub 2020 Feb 10.

Abstract

Plasma kallikrein (PKal) belongs to the family of trypsin-like serine proteases. The expression of PKal is associated with multiple physiological systems or pathways such as coagulation pathway, platelet aggregation process, kallikrein-kinin system, renin-angiotensin system and complement pathway. On the basis of PKal's multiple physiological functions, it has been considered as a potential target for several diseases including hereditary angioedema, microvascular complications of diabetes mellitus and cerebrovascular disease. Up to now, many PKal inhibitors have been identified and a few of them have reached clinical trials or market. This review summarizes the development of small molecule and peptide PKal inhibitors having different scaffolds and discusses their structure-activity relationship and selectivity. We hope this review facilitates a comprehensive understanding of the types of PKal inhibitors developed to tackle different manifestations of PKal-associated diseases.

Keywords: Factor XI; Hereditary angioedema; Plasma kallikrein inhibitor; Selectivity; Structure activity relationship.

Publication types

  • Review

MeSH terms

  • Animals
  • Catalytic Domain
  • Drug Discovery
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / metabolism
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Molecular Structure
  • Plasma Kallikrein / antagonists & inhibitors*
  • Plasma Kallikrein / chemistry
  • Plasma Kallikrein / metabolism
  • Protein Binding
  • Structure-Activity Relationship

Substances

  • Enzyme Inhibitors
  • Plasma Kallikrein