GC-MS metabolite profiling and multi-target Docking analysis of Calotropis procera and Euphorbia tirucalli stem extracts for cytotoxicity and antioxidant activity

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Authors: Gashaw Nigussie, Sumera Zaib, Menberework Chanyalew, Aman Dekebo, Asfaw Meressa, Markos Abebe, Temesgen Negassa, Mo Hunsen, Milkyas Endale
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References: 54

Abstract

C. procera and E. tirucalli are traditionally used to treat infections, inflammation, skin disorders, and tumors. This study evaluated their cytotoxic and antioxidant activities, analyzed chemical profiles via GC-MS, and performed molecular docking against breast cancer target proteins. The methanol extracts of C. procera and E. tirucalli stems inhibited the growth of MCF-7 breast cancer cells by 31.0 ± 0.98% and 36.0 ± 0.31%, respectively, at a concentration of 200 µg/mL, with corresponding IC₅₀ values of 102.31 and 130.12 µg/mL. Both methanol and n-hexane stem extracts showed significant antioxidant activity in DPPH and ABTS assays. In the DPPH assay, IC₅₀ values for C. procera were 10.79 µg/mL (methanol) and 18.52 µg/mL (n-hexane), while for E. tirucalli, values were 33.76 µg/mL and 12.37 µg/mL, respectively. In the ABTS assay, IC₅₀ values were 7.24 µg/mL (methanol) and 11.98 µg/mL (n-hexane) for C. procera, and 8.97 µg/mL (methanol) and 23.52 µg/mL (n-hexane) for E. tirucalli. GC-MS analysis revealed key phytochemicals including α-amyrin, β-amyrin, lanosterol, germanicol, lupeol, olean-18-ene, linoleic acid, and oleic acid. Compounds with relative abundance ≥ 1% were analyzed using SwissADME and ProTox II, revealing compliance with Lipinski’s rule of five and no predicted hepatotoxicity, carcinogenicity, mutagenicity, or cytotoxicity. Molecular docking analysis showed that lupeol, β-amyrin, α-amyrin, lanosterol, olean-18-ene, and germanicol had strong binding affinities with human myeloperoxidase (-10.1 to -10.8 kcal/mol) and estrogen receptor alpha (-7.5 to -9.9 kcal/mol), outperforming reference compounds ascorbic acid (-5.8 kcal/mol) and gefitinib (-7.5 kcal/mol). These findings suggest C. procera and E. tirucalli are promising sources of bioactive compounds, supporting their potential for further in vivo and mechanistic investigations in drug development.

Fields of Study & Subjects

Phytochemistry and Bioactive Compounds Bioactive Natural Diterpenoids Research Phytochemistry and Biological Activities

Publication details

Journal / source
Scientific Reports
Volume
16
Issue
1
Pages
2954–2954
Publication date
6 January 2026
Language
EN