Back to Search
Start Over
Chromone-based small molecules for multistep shutdown of arachidonate pathway: Simultaneous inhibition of COX-2, 15-LOX and mPGES-1 enzymes.
- Source :
-
European Journal of Medicinal Chemistry . Feb2024, Vol. 266, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- As a new approach to the management of inflammatory disorders, a series of chromone-based derivatives containing a (carbamate)hydrazone moiety was designed and synthesized. The compounds were assessed for their ability to inhibit COX-1/2, 15-LOX, and mPGES-1, as a combination that should effectively impede the arachidonate pathway. Results revealed that the benzylcarbazates (2a-c) demonstrated two-digit nanomolar COX-2 inhibitory activities with reasonable selectivity indices. They also showed appreciable 15-LOX inhibition, in comparison to quercetin. Further testing of these compounds for mPGES-1 inhibition displayed promising activities. Intriguingly, compounds 2a-c were capable of suppressing edema in the formalin-induced rat paw edema assay. They exhibited an acceptable gastrointestinal safety profile regarding ulcerogenic liabilities in gross and histopathological examinations. Additionally, upon treatment with the test compounds, the expression of the anti-inflammatory cytokine IL-10 was elevated, whereas that of TNF-α, iNOS, IL-1β, and COX-2 were downregulated in LPS-challenged RAW264.7 macrophages. Docking experiments into the three enzymes showed interesting binding profiles and affinities, further substantiating their biological activities. Their in silico physicochemical and pharmacokinetic parameters were advantageous. [Display omitted] • A new series of chromone-acylhydrazones was designed and synthesized. • Benzylcarbazates 2a-c proved to be triple inhibitors of COX-2, 15-LOX and mPGES-1. • In cellular assay, they reduced pro-inflammatory mediators similarly to celecoxib. • They decreased formalin-induced rat paw edema in vivo without ulcerogenic effects. • Benzylcarbazates 2a-c could be promising multipotent anti-inflammatory prototypes. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 02235234
- Volume :
- 266
- Database :
- Academic Search Index
- Journal :
- European Journal of Medicinal Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 175194169
- Full Text :
- https://doi.org/10.1016/j.ejmech.2024.116138