Phytochemical profile of Cespedesia spathulata leaves (Ochnaceae) and its effect on tyrosinase enzyme
Phytochemical studies of Cespedesia spathulata (Ochnaceae) leaves using H-1, C-13 NMR, and GC-MS have led to the isolation of some metabolites identified for the first time in these species such as cathechin, epicatechin, vitexin, orientin, 6 ''-O-acetyl-vitexin, sitosterol, stigmasterol,...
Gespeichert in:
Veröffentlicht in: | Anais da Academia Brasileira de Ciências 2021-01, Vol.93 (4), p.e20200443-e20200443, Article 20200443 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Phytochemical studies of Cespedesia spathulata (Ochnaceae) leaves using H-1, C-13 NMR, and GC-MS have led to the isolation of some metabolites identified for the first time in these species such as cathechin, epicatechin, vitexin, orientin, 6 ''-O-acetyl-vitexin, sitosterol, stigmasterol, phytol, 4,5-dihydrovomifoliol and a mixture of aliphatic methyl esters, together with ochnaflavone, which was previously isolated from this plant. The modulating activity of some fractions and compounds from Cespedesia spathulata towards tyrosinase enzyme was assayed by spectroscopic and theoretical means/experiments. The dichloromethane fraction (133 mu g mL(-1)) and ochnaflavone (333 mu M) inhibited tyrosinase activity by 20 % and 2.0 %, respectively, whereas the ethyl acetate fraction (666 mu g mL(-1)) and +/- catechins (catechin and epicatechin - 800 mu M) activated it by 104 % and 384 %, respectively. Quantum chemical calculations suggested that catechin and epicatechin are better activators than L-DOPA by interacting with Cu (II) ions. Molecular docking results suggested that hydrogen bonding and hydrophobic interactions are the main binding forces between each tyrosinase activator and the amino acid residues inside the active protein binding pocket. |
---|---|
ISSN: | 0001-3765 1678-2690 1678-2690 |
DOI: | 10.1590/0001-3765202120200443 |