Rotational constriction of curcuminoids impacts 5-lipoxygenase and mPGES-1 inhibition and evokes a lipid mediator class switch in macrophages.
Arachidonate 5-Lipoxygenase
/ metabolism
Constriction
Curcumin
/ metabolism
Diarylheptanoids
/ metabolism
Eicosanoids
/ metabolism
Humans
Leukotrienes
Lipoxygenase Inhibitors
/ pharmacology
Macrophages
/ metabolism
Molecular Docking Simulation
Prostaglandin-E Synthases
/ antagonists & inhibitors
Prostaglandins
/ metabolism
Curcumin
Inflammation
Leukotriene
Lipid mediators
Natural product
Structure–activity relationship
Journal
Biochemical pharmacology
ISSN: 1873-2968
Titre abrégé: Biochem Pharmacol
Pays: England
ID NLM: 0101032
Informations de publication
Date de publication:
09 2022
09 2022
Historique:
received:
18
05
2022
revised:
28
07
2022
accepted:
29
07
2022
pubmed:
7
8
2022
medline:
25
8
2022
entrez:
6
8
2022
Statut:
ppublish
Résumé
Polypharmacological targeting of lipid mediator networks offers potential for efficient and safe anti-inflammatory therapy. Because of the diversity of its biological targets, curcumin (1a) has been viewed as a privileged structure for bioactivity or, alternatively, as a pan-assay interference (PAIN) compound. Curcumin has actually few high-affinity targets, the most remarkable ones being 5-lipoxygenase (5-LOX) and microsomal prostaglandin E
Identifiants
pubmed: 35932797
pii: S0006-2952(22)00296-9
doi: 10.1016/j.bcp.2022.115202
pii:
doi:
Substances chimiques
Diarylheptanoids
0
Eicosanoids
0
Leukotrienes
0
Lipoxygenase Inhibitors
0
Prostaglandins
0
Arachidonate 5-Lipoxygenase
EC 1.13.11.34
PTGES protein, human
EC 5.3.99.3
Prostaglandin-E Synthases
EC 5.3.99.3
Curcumin
IT942ZTH98
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
115202Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.