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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.
Ragab, Ahmed; Elsisi, Doaa M; Elqady, Enayat M; El-Said, Eman; Salem, Mohamed A; Ammar, Yousry A; Abusaif, Moustafa S.
Afiliação
  • Ragab A; Department of Chemistry, Faculty of Science (Boys), Al-Azhar University, 11884 Nasr City, Cairo, Egypt. Electronic address: ahmed_ragab@azhar.edu.eg.
  • Elsisi DM; Department of Chemistry, Faculty of Science (Girls), Al-Azhar University, 11754 Nasr City, Cairo, Egypt.
  • Elqady EM; Zoology and Entomology Department, Faculty of Science, Al-Azhar University (Girls), Cairo, Egypt.
  • El-Said E; Zoology and Entomology Department, Faculty of Science, Al-Azhar University (Girls), Cairo, Egypt.
  • Salem MA; Department of Chemistry, Faculty of Science and Arts, King Khalid University, Mohail, Assir, Saudi Arabia.
  • Ammar YA; Department of Chemistry, Faculty of Science (Boys), Al-Azhar University, 11884 Nasr City, Cairo, Egypt.
  • Abusaif MS; Department of Chemistry, Faculty of Science (Boys), Al-Azhar University, 11884 Nasr City, Cairo, Egypt.
Pestic Biochem Physiol ; 202: 105943, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38879303
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 (LC50) and the lethal time values (LT50). 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 LC50 = 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 (LT50) 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quinoxalinas / Spodoptera / Inseticidas / Larva Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quinoxalinas / Spodoptera / Inseticidas / Larva Idioma: En Ano de publicação: 2024 Tipo de documento: Article