Styrylchromones: Biological Activities and Structure-Activity Relationship.

2-styrylchromones 3-styrylchromones Biological Activity Structure-Activity Relationship

Journal

ChemMedChem
ISSN: 1860-7187
Titre abrégé: ChemMedChem
Pays: Germany
ID NLM: 101259013

Informations de publication

Date de publication:
31 Oct 2024
Historique:
revised: 28 10 2024
received: 30 09 2024
accepted: 29 10 2024
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 31 10 2024
Statut: aheadofprint

Résumé

Styrylchromones (SC) are a group of oxygen-containing heterocyclic compounds, which are characterized by the attachment of a styryl group to the chromone core. SC can be found in nature or can be chemically synthesized in the laboratory. As their presence in nature is scarce, the synthetic origin is the most common. Two types of SC are known: 2-styrylchromones and 3-styrylchromones. However, 2-styrylchromones are the most common, being more commonly found in nature and which chemical synthesis is more commonly described. A wide variety of SC has been described in the literature, with different substituents in different positions, the majority of which are distributed on the A- and/or B-rings. Over the years, several biological activities have been attributed to SC. This work presents a comprehensive review of the biological activities attributed to SC and their structure-activity relationship, based in a published literature search, since 1989. The following biological activities are thoroughly revised and discussed in this review: antioxidant, antiallergic, antiviral, antibacterial, antifungal, anti-inflammatory and antitumoral, affinity and selectivity for A3 adenosine receptors, neuroprotective, and α-glucosidase inhibition. In general, SC are composed by a promising scaffold with great potential for the development of new drugs.

Identifiants

pubmed: 39480961
doi: 10.1002/cmdc.202400782
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202400782

Informations de copyright

© 2024 Wiley‐VCH GmbH.

Auteurs

Mariana Lucas (M)

REQUIMTE LAQV Porto, Faculty of Pharmacy, University of Porto, PORTUGAL.

Marisa Freitas (M)

REQUIMTE LAQV Porto, Faculty of Pharmacy, University of Porto, PORTUGAL.

Artur M S Silva (AMS)

REQUIMTE LAQV Porto, Department of Chemistry, University of Aveiro, PORTUGAL.

Eduarda Fernandes (E)

REQUIMTE LAQV Porto, , Faculty of Pharmacy, University of Porto, PORTUGAL.

Daniela Ribeiro (D)

University of the Azores, School of Agrarian and Environmental Sciences, Rua Capitão João d'Ávila, 9700-042, Angra do Heroísmo, PORTUGAL.

Classifications MeSH