Mesua sp.: chemical aspects and pharmacological relevance of prenylated polyphenols

TitreMesua sp.: chemical aspects and pharmacological relevance of prenylated polyphenols
Type de publicationArticle de revue
AuteurRouger, Caroline , Derbré, Séverine , Richomme, Pascal
EditeurSpringer Verlag
TypeArticle scientifique dans une revue à comité de lecture
Année2019
LangueAnglais
DateFévrier 2019
Numéro1
Pagination317-342
Volume18
Titre de la revuePhytochemistry Reviews
ISSN1568-7767
Mots-clésimmunomodulation, Mammea coumarins, Mesua L., Prenylated polyphenols, Xanthones
Résumé en anglais

The genus Mesua L. (Calophyllaceae) comprises approximately 50 species that grow in the restrictive area of South East Asia. Investigations of Mesua species reported the chemodiversity and pharmacological relevance of their phytoconstituents, in particular polyphenolic compounds. To date, about 170 secondary metabolites have been identified from 13 Mesua species, predominantly xanthones and coumarins. Most of them hold a prenylated skeleton and display activities such as antitumor and antimicrobial, antioxidant, anti-inflammatory or immunomodulating properties, which were evaluated using either in vitro assay or, in rare cases, in vivo animal studies. Prenylation of aromatic compounds appears as a key element to enhance their biological activities, including their cytotoxicity and, could be involved in their inhibitory potential towards enzymes playing crucial roles in inflammatory and immune cascades. The aim of this review is to provide a systematic and comprehensive overview of Mesua polyphenolic secondary metabolites and their pharmacological properties. Among them, the structure of coumarin beccamarin T is herein revised and attributed to lepidotol A based on a careful examination of the 1D and 2D NMR spectra of the respective compounds. A considerable attention is also given to the place of prenylated polyphenols as anti-inflammatory and immunomodulatory molecules, to highlight the interest of Mesua metabolites as chemical probes for target discovery.

URL de la noticehttp://okina.univ-angers.fr/publications/ua18657
DOI10.1007/s11101-018-9594-9
Lien vers le document

https://link.springer.com/article/10.1007%2Fs11101-018-9594-9