The Chromenopyridine Scaffold: A Privileged Platform in Drug Design.
biological activity
chromene
chromenopyridine
pyridine
synthesis
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
25 Jun 2024
25 Jun 2024
Historique:
received:
23
04
2024
revised:
07
06
2024
accepted:
19
06
2024
medline:
13
7
2024
pubmed:
13
7
2024
entrez:
13
7
2024
Statut:
epublish
Résumé
The chromenopyridine scaffold represents an important class of heterocyclic compounds exhibiting a broad spectrum of biological properties. This review describes novel and efficient procedures for the synthesis of this scaffold. Herein, several methods were detailed and grouped according to their starting material (e.g., salicylaldehydes, chromones, chromanones and coumarins) and respective biological activity, when reported. This review highlights the potential of the reported synthetic strategies for preparing chromenopyridine derivatives with promising biological activity, paving the way for further developments in drug discovery.
Identifiants
pubmed: 38998955
pii: molecules29133004
doi: 10.3390/molecules29133004
pii:
doi:
Substances chimiques
Pyridines
0
Chromones
0
Coumarins
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM