Proteinase 3 phosphonic inhibitors.
Activity-based probes
Aminophosphonates
Inhibitors
Neutrophil serine proteases
Proteinase 3
Journal
Biochimie
ISSN: 1638-6183
Titre abrégé: Biochimie
Pays: France
ID NLM: 1264604
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
12
02
2019
accepted:
07
03
2019
pubmed:
17
3
2019
medline:
31
12
2019
entrez:
17
3
2019
Statut:
ppublish
Résumé
Neutrophils are one of the most important military services of the armed forces of the immune system, a crucial line of defense against bacterial or fungal onslaughts. One of their mechanisms of action relies on the production of serine proteases. One of these enzymes is proteinase 3 (PR3), which is engaged in the processing of pro-inflammatory cytokines, receptors, heat shock proteins and in the generation of antibacterial peptides. Despite its protective function, uncontrolled activity of PR3 has been associated with the progression of inflammation and tissue injury. Although PR3 was characterized at the beginning of 90's of the last century for the first time, the research on the development of its inhibitors is barely noticeable. Here we present the recent findings on the design, synthesis and the activity of phosphonic PR3 inhibitors together with the historical perspective.
Identifiants
pubmed: 30876969
pii: S0300-9084(19)30072-0
doi: 10.1016/j.biochi.2019.03.005
pii:
doi:
Substances chimiques
Organophosphonates
0
Serine Proteinase Inhibitors
0
Myeloblastin
EC 3.4.21.76
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
142-149Informations de copyright
Copyright © 2019 Elsevier B.V. and Société Française de Biochimie et Biologie Moléculaire (SFBBM). All rights reserved.