4.6 Article

GC-MS/MS Quantification of EGFR Inhibitors, β-Sitosterol, Betulinic Acid, (+) Eriodictyol, (+) Epipinoresinol, and Secoisolariciresinol, in Crude Extract and Ethyl Acetate Fraction of Thonningia sanguinea

Journal

MOLECULES
Volume 27, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/molecules27134109

Keywords

Thonningia sanguinea; GC-MS; MS; eriodictyol; secoisolariciresinol; EGFR

Funding

  1. Deanship of Scientific Research (DSR) at King Abdulaziz University, Jeddah, Saudi Arabia [G-549-166-1439]

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Thonningia sanguinea Vahl, a widely used medicinal plant in African traditional medicine, was analyzed for its chemical composition and its potential as an adjuvant therapy in cancer treatments. Gas chromatography combined with tandem mass spectrometry was used to quantify the contents of several compounds in the plant extract, and molecular docking studies revealed the binding interactions of these compounds with the epidermal growth factor receptor (EGFR). The results suggest that certain compounds in T. sanguinea have high binding affinities with EGFR and have the potential to be used in cancer treatments.
Medicinal plants are widely used in folk medicine to treat various diseases. Thonningia sanguinea Vahl is widespread in African traditional medicine, and exhibits antioxidant, antibacterial, antiviral, and anticancer activities. T. sanguinea is a source of phytomedicinal agents that have previously been isolated and structurally elucidated. Herein, gas chromatography combined with tandem mass spectrometry (GC-MS/MS) was used to quantify epipinoresinol, beta-sitosterol, eriodictyol, betulinic acid, and secoisolariciresinol contents in the methanolic crude extract and its ethyl acetate fraction for the first time. The ethyl acetate fraction was rich in epipinoresinol, eriodictyol, and secoisolariciresinol at concentrations of 2.3, 3.9, and 2.4 mg/g of dry extract, respectively. The binding interactions of these compounds with the epidermal growth factor receptor (EGFR) were computed using a molecular docking study. The results revealed that the highest binding affinities for the EGFR signaling pathway were attributed to eriodictyol and secoisolariciresinol, with good binding energies of -19.93 and -16.63 Kcal/mol, respectively. These compounds formed good interactions with the key amino acid Met 769 as the co-crystallized ligand. So, the ethyl acetate fraction of T. sanguinea is a promising adjuvant therapy in cancer treatments.

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