New Prospective Insecticidal Agents Based on N-(arylcarbamothioyl)arylmide Derivatives Against Spodoptera frugiperda: Design, Synthesis, Toxicological, Biological, Biomedical Studies and Antibacterial Activity.

Autor: Khalaf MM; Department of Chemistry, College of Science, King Faisal University, Al-Ahsa, 31982, Saudi Arabia.; Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt., Abd El-Lateef HM; Department of Chemistry, College of Science, King Faisal University, Al-Ahsa, 31982, Saudi Arabia.; Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt., Gouda M; Department of Chemistry, College of Science, King Faisal University, Al-Ahsa, 31982, Saudi Arabia., Almarri MN; Department of Chemistry, College of Science, King Faisal University, Al-Ahsa, 31982, Saudi Arabia., Abdelhamid AA; Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt.; Chemistry Department, Faculty of Science, Al-Baha University, Al-Baha, Saudi Arabia., Al-Ghamdi S; Biology Department, Faculty of Science, Al-Baha University, Al-Baha, Saudi Arabia., Amer AA; Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt., Gad MA; Research Institute of Plant Protection, Agricultural Research Center, Giza, 12619, Egypt.
Jazyk: angličtina
Zdroj: Chemistry & biodiversity [Chem Biodivers] 2024 Nov; Vol. 21 (11), pp. e202401310. Date of Electronic Publication: 2024 Sep 09.
DOI: 10.1002/cbdv.202401310
Abstrakt: In this work, a novel series of N-(arylcarbamothioyl)arylmide) 2-11 were synthesized by treating One-Pot three-multicomponent of Aroyl chloride, ammonium isothiocyanate and amine compounds under refluxing conditions. Using spectroscopic methods, the chemical structure of the novelty developed compounds were investigated. After five days, the proposed derivatives' insecticidal bioassay was assessed using the median lethal concentration (LC 50 ) against the second & fourth larvae of Spodoptera frugiperda as toxicity agents. The findings showed that, to varying degrees, every tested substance exerted insecticidal effects on S. frugiperda larvae in both of their instars. Compound 9 was the most poisonous of them all, having an LC 50 against larvae in their second and fourth instars of 60.45 and 123.21 mg/L, respectively. Additionally, a few biological and biochemical characteristics of the substances that were generated in a lab setting were also looked at. Furthermore, this work discusses how to discover novel compounds that may one day be employed as insecticidal agents. Finally, all the designed components were monitored for their antibacterial effectiveness toward both Gram-positive & Gram-negative bacteria.
(© 2024 Wiley-VHCA AG, Zurich, Switzerland.)
Databáze: MEDLINE
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