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Artocarpus lacucha, a plant in the Moraceae family, has traditionally been used in Southeast Asian medicine to treat various ailments. This study investigated the insecticidal potential against Spodoptera litura of several compounds extracted from A. lacucha using a topical application method. A sequential extraction method was employed with A. lacucha stems to identify the most toxic crude extract by using hexane, dichloromethane, ethyl acetate, and methanol solvents. Subsequently, the most toxic crude extract was analyzed for chemical composition by HPLC, followed by the isolation process. Among these crude extracts, the ethyl acetate crude extract was the most toxic to second-instar S. litura larvae (24-h LD50 value of ∼9.07 µg/larva). Our results showed that the catechin isolated from the ethyl acetate crude extract exhibited the highest toxicity against this insect (24-h LD50 value of ∼8.37 µg/larva). Additionally, catechin significantly decreased the activities of acetylcholinesterase, carboxylesterases, and glutathione S-transferase in the larvae. These findings suggest that catechin isolated from A. lacucha could be a potential insecticidal agent against S. litura. However, the toxicity and persistence of catechin under field conditions need to be further investigated to develop this novel insecticide. [ABSTRACT FROM AUTHOR]

The discovery of eco-friendly plant-based insecticides is currently booming in research with an attempt to replace synthetic chemical insecticides causing tremendous adverse effects. The present work studied the insecticidal potential of ginger, an important medicinal plant. Four crude extracts from Zingiber officinale rhizomes were evaluated for their contact toxicity against second instars of Spodoptera litura, Spodoptera exigua and Spodoptera frugiperda using the topical application. The hexane extract exhibited the strongest toxicity to S. exigua with the LD50 of 9.92 and 8.40 µg/larva at 24 and 48 h posttreatment, respectively, followed by S. frugiperda. Comparative toxicity of the most abundant secondary metabolites from the hexane extract, gingerols and shogaols, against both insects concluded that 8-shogaol (5) was identified as the most active compound against S. frugiperda with the LD50 of 7.68 and 3.96 µg/larva at 24 and 48 h posttreatment, respectively. [ABSTRACT FROM AUTHOR]

Phytochemical investigation of Artocarpus lacucha Buch.-Ham (Moraceae) leaves led to the identification of three of the rarely found flavan-benzofuranes named artocarpinol C ( 1 ), 3- epi -artocarpinol C ( 2 ), and artocarpinol D ( 6 ) along with six known flavan derivatives. Thus, a total of six artocarpinols are now described. All their chemical structures and absolute configurations were established by one dimensional (1D)- and two-dimensional (2D) NMR, infrared (IR), electronic circular dichroism (ECD), high-resolution electrospray ionisation mass spectrometry (HR-ESI-MS), and optical rotation (OR). Density functional theory (DFT) calculations based on the B3LYP theory level were conducted to determine the stereochemistry at positions 2 and 3 in the C-ring. All compounds exhibited in vitro radical scavenging activities, and compounds 3 and 5 demonstrated pronounced intracellular antioxidative effects in colon carcinoma cells (SW480), as determined by the DCFH-DA assay. Compounds 3 and 5 exhibited further high affinities for binding to the active site of human glutathione reductase. These molecular properties are discussed with regard to possible applications., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)