Department of Chemistry, Faculty of Science (Boys), Al-Azhar University, 11884 Nasr City, Cairo, Egypt.
Department of Chemistry, Faculty of Science (Girls), Al-Azhar University, 11754 Nasr City, Cairo, Egypt.
Pestic Biochem Physiol. 2024 Jun;202:105943. doi: 10.1016/j.pestbp.2024.105943. Epub 2024 May 6.
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) and the lethal time values (LT). 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 = 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) 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.
在这项研究中,通过回流条件下用硫代半卡巴腙和硫脲衍生物处理 2,3-二氯喹喔啉,合成了一系列新的噻唑并[4,5-b]喹喔啉衍生物 3-8。新设计的衍生物的化学结构是通过光谱技术进行的。设计衍生物的杀虫生物测定是通过中致死浓度(LC)和致死时间值(LT),在五天后作为毒性剂评估对 S. litura 的第 2 和第 4 幼虫的影响。结果表明,所有测试化合物对 S. litura 的两个龄期幼虫都具有杀虫作用,具有不同的活性。其中,噻唑并[4,5-b]喹喔啉衍生物 3 的毒性最高,对第 2 和第 4 龄幼虫的 LC 值分别为 261.88 和 433.68 ppm。此外,噻唑并[4,5-b]喹喔啉衍生物 3 杀死 50%种群所需的时间最短(LT),2 龄幼虫分别为 20.88、13.2 和 15.84 小时,浓度分别为 625、1250 和 2500 ppm,而 4 龄幼虫分别为 2.75、2.08 和 1.76 天,浓度分别为 625、1250 和 2500 ppm。对最活跃的衍生物 3 进行了幼虫形态和组织学研究。根据 SEM 分析,发现外角质层和头壳的形态受到影响。此外,在角质层和中肠组织中还存在一些组织学变化。柱状细胞开始分解,围食膜发生空泡化。此外,用化合物 3 处理第 4 龄 S litura 幼虫的血淋巴,在生化分析中显示出显著变化,如总蛋白、GPT、GOT、乙酰胆碱酯酶(AChE)和碱性磷酸酶(AlP)。最后,对最活跃的衍生物进行毒性预测,结果表明其无腐蚀性、对眼睛无刺激性、无呼吸毒性、对皮肤无敏感性、无肝毒性,并且对小鱼毒性和 T. pyriformis 无毒性,表明对人类具有良好的毒性特征。