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New prospective insecticidal agents based on thiazolo[4,5-b]quinoxaline derivatives against cotton leafworm Spodoptera litura (Fabricius): Design, synthesis, toxicological, morphology, histological, and biomedical studies.
- Source :
-
Pesticide biochemistry and physiology [Pestic Biochem Physiol] 2024 Jun; Vol. 202, pp. 105943. Date of Electronic Publication: 2024 May 06. - Publication Year :
- 2024
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Abstract
- In this study, a new series of thiazolo[4,5-b]quinoxaline derivatives 3-8 were synthesized by treating 2,3-dichloroquinoxaline with thiosemicarbazone and thiourea derivatives under reflux conditions. The chemical structure of the newly designed derivatives was conducted using spectroscopic techniques. The insecticidal bioassay of the designed derivatives was evaluated against the 2nd and 4th larvae of S. litura after five days as toxicity agents via median lethal concentration (LC <subscript>50</subscript> ) and the lethal time values (LT <subscript>50</subscript> ). The results indicated that all the tested compounds had insecticidal effects against both instar larvae of S. litura with variable values. Among them, thiazolo[4,5-b]quinoxaline derivative 3 was the most toxic, with LC <subscript>50</subscript>  = 261.88 and 433.68 ppm against 2nd and 4th instar larvae, respectively. Moreover, the thiazolo[4,5-b]quinoxaline derivative 3 required the least time to kill the 50% population (LT <subscript>50</subscript> ) of 2nd larvae were 20.88, 13.2, and 15.84 hs with 625, 1250, and 2500 ppm, respectively, while for the 4th larval instar were 2.75, 2.08, and 1.76 days with concentrations of 625, 1250, and 2500 ppm, respectively. Larvae's morphological and histological studies for the most active derivative 3 were investigated. According to SEM analysis, the exterior morphology of the cuticle and head capsule was affected. In addition, there were some histological alterations in the cuticle layers and the midgut tissues. Columnar cells began breaking down, and vacuolization occurred in the peritrophic membrane. Moreover, treating 4th S litura larvae hemolymph with compound 3 showed significant changes in biochemical analysis, such as total proteins, GPT, GOT, acetylcholinesterase (AChE), and alkaline phosphatase (AlP). Finally, the toxicity prediction of the most active derivative revealed non-corrosive, non-irritant to the eye, non-respiratory toxicity, non-sensitivity to the skin, non-hepatotoxic, and don't have toxicity on minnow toxicity and T. pyriformis indicating a good toxicity profile for human.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Thiazoles chemistry
Insecticides chemical synthesis
Insecticides pharmacology
Insecticides toxicity
Insecticides chemistry
Quinoxalines toxicity
Quinoxalines pharmacology
Quinoxalines chemical synthesis
Quinoxalines chemistry
Larva drug effects
Spodoptera drug effects
Spodoptera growth & development
Subjects
Details
- Language :
- English
- ISSN :
- 1095-9939
- Volume :
- 202
- Database :
- MEDLINE
- Journal :
- Pesticide biochemistry and physiology
- Publication Type :
- Academic Journal
- Accession number :
- 38879303
- Full Text :
- https://doi.org/10.1016/j.pestbp.2024.105943