Molecular Networking-Driven Discovery of Carapins A–H, Bioactive Limonoids from Carapa macrantha Harms (Meliaceae)

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Authors: Steveng Schüller Kamgni Tiogo, Flaure Rosette Ehawa Essoung, Joël Eddy Terence Ateba, Appolinaire Kene Dongmo, Lauve Rachel Tchokouaha Yamthé, William F. Feudjou, Jean Jules Kezetas Bankeu, Hans‐Georg Stammler, Marcus Persicke, Fabrice Fekam Boyom, Jean Rodolphe Chouna, Norbert Sewald
+2 more Alembert Tiabou Tchinda, Bruno Ndjakou Lenta
Cited by: 1
References: 41

Abstract

Molecular networking-driven investigation of the root, stem bark, and fruit extracts of the medicinal plant Carapa macrantha led to the targeted isolation of seven previously undescribed limonoids ( 1 – 7 ), one new pregnane-type steroid ( 8 ), and 17 known compounds ( 9 – 25 ). Structural elucidation was achieved using spectroscopic methods, single-crystal X-ray analyses, and comparison with literature data. Extracts and isolated compounds were assessed in vitro for antiplasmodial activity against the chloroquine-sensitive 3D7 and the multidrug-resistant Dd2 strains of Plasmodium falciparum ( Pf 3D7 and Pf Dd2). The dichloromethane (CH 2 Cl 2 )/methanol (MeOH) (1:1) root extract showed significant activity against Pf Dd2, with an IC 50 value of 10 ± 2 μg/mL and good selectivity over Vero cells (SI > 10). Compounds, 6, 7, 9, 10, and 17 exhibited the best activity, with IC 50 values ranging from 5.7 to 22.9 μM against both strains. Compound 17 was the most active one on both strains, with IC 50 values of 5.7 ± 0.4 and 9.4 ± 0.4 μM against Pf 3D7 and Pf Dd2 with SI > 7, respectively. These findings highlight C. macrantha as a potential source of antiplasmodial agents.

Fields of Study & Subjects

Phytochemical compounds biological activities Synthesis and bioactivity of alkaloids Phytochemistry and Bioactivity Studies

Publication details

Journal / source
Journal of Natural Products
Publisher
American Chemical Society (ACS)
Volume
89
Issue
2
Pages
506–518
Publication date
17 February 2026
Language
EN