Chemical Characterization of Plant Extracts and Evaluation of their Nematicidal and Phytotoxic Potential

Chemical Characterization of Plant Extracts and Evaluation of their Nematicidal and Phytotoxic Potential

Raúl Velasco-Azorsa, Héctor Cruz-Santiago, Ignacio Cid del Prado-Vera, Marco Vinicio Ramirez-Mares, María del Rocío Gutiérrez-Ortiz, Norma Francenia Santos-Sánchez, Raúl Salas-Coronado, Claudia Villanueva-Cañongo, Karla Isabel Lira-de León, Beatriz Hernández-Carlos

Nacobbus aberrans ranks among the “top ten” plant-parasitic nematodes of phytosanitary importance. It causes significant losses in commercial interest crops in America and is a potential risk in the European Union. The nematicidal and phytotoxic activities of seven plant extracts against N. aberrans and Solanum lycopersicum were evaluated in vitro, respectively. The chemical nature of three nematicidal extracts (EC50,48h ≤ 113 µg mL−1) was studied through NMR analysis. Plant extracts showed nematicidal activity on second-stage juveniles (J2): (≥87%) at 1000 µg mL−1 after 72 h, and their EC50 values were 71.4–468.1 and 31.5–299.8 µg mL−1 after 24 and 48 h, respectively. Extracts with the best nematicidal potential (EC50,48h < 113 µg mL−1) were those from Adenophyllum aurantium, Alloispermum integrifolium, and Tournefortia densiflora, which inhibited L. esculentum seed growth by 100% at 20 µg mL−1. Stigmasterol (1), β-sitosterol (2), and α-terthienyl (3) were identified from A. aurantium, while 1, 2, lutein (4), centaurin (5), patuletin-7-β-O-glucoside (6), pendulin (7), and penduletin (8) were identified from A. integrifolium. From T. densiflora extract, allantoin (9), 9-O-angeloyl-retronecine (10), and its N-oxide (11) were identified. The present research is the first to report the effect of T. densiflora, A. integrifolium, and A. aurantium against N. aberrans and chemically characterized nematicidal extracts that may provide alternative sources of botanical nematicides.

2021

9-<i>O</i>-angeloyl-retronecine N-oxide, <i>Nacobbus aberrans</i>, Quercetagetin derivatives, nematicidal activity, stigmasterol, α-terthienyl

10.3390/molecules26082216

Molecules

MDPI AG

Organic chemistry