Silva Everton P, Luz-Filho Agenor P, Sousa Abraão P, Alencar-Filho Edilson B, Santos Vanessa C, Silva Luana B R, Lima Priscila S V, Souza Helivaldo D S, Athayde-Filho Petrônio F, Fiss Gabriela F
Department of Chemistry, Universidade Federal da Paraíba (UFPB), João Pessoa 58051-900, Brazil.
Department of Pharmaceutical Sciences, Universidade Federal do Vale do São Francisco (UNIVASF), Petrolina 56304-917, Brazil.
ACS Omega. 2025 Aug 15;10(33):37906-37915. doi: 10.1021/acsomega.5c05060. eCollection 2025 Aug 26.
, the main transmitter of arboviruses responsible for several arboviruses, such as dengue, is highly prevalent in Latin America, especially in Brazil. Controlling this vector is urgent for public health, since it is more advantageous to prevent than to treat the diseases it causes. The use of chemical control methods, such as larvicides, is strategic. In this sense, the search for environmentally safer larvicides has driven the development of compounds with activity against and low toxicity to nontarget organisms. In this study, a rational design of ten 4-alkoxy/amino-7-chloroquinolines was carried out to investigate their larvicidal and toxic properties, from prediction to assays. Larvicidal tests revealed seven bioactives against (LC ≤ 69.18 ppm), of which compound was very active (LC = 2.51 ppm) and compound was very highly active (LC = 0.02 ppm), surpassing the standard larvicide Spinosad (LC = 0.05 ppm). Structural analysis indicated that the -O-pentyl and -O-ethyl-Cl moieties at the 4-position of 7-chloroquinolines improved larvicidal activity when compared to 4,7-dichloroquinoline. Regarding the ecotoxicity study, bioactives , , , and showed moderate toxicity on larvae (LC = 101.68-314.58 μg·mL). The best results demonstrated that compound , potentially nonmutagenic, nonhepatotoxic, and predicted not to cause skin sensitization, was 15 729 times more toxic to than to the nontarget organism , emerging as a safer larvicide.
负责传播多种虫媒病毒(如登革热病毒)的主要传播媒介在拉丁美洲,尤其是巴西高度流行。控制这种病媒对公共卫生至关重要,因为预防其所引发的疾病比治疗更为有利。使用化学控制方法,如杀幼虫剂,具有战略意义。从这个意义上讲,寻找对环境更安全的杀幼虫剂推动了对非靶标生物具有活性且低毒的化合物的开发。在本研究中,对十种4-烷氧基/氨基-7-氯喹啉进行了合理设计,以研究它们从预测到实验的杀幼虫和毒性特性。杀幼虫试验显示七种对[某种蚊虫]具有生物活性(LC₅₀≤69.18 ppm),其中化合物[具体编号]活性很强(LC₅₀ = 2.51 ppm),化合物[具体编号]活性极高(LC₅₀ = 0.02 ppm),超过了标准杀幼虫剂多杀菌素(LC₅₀ = 0.05 ppm)。结构分析表明,与4,7-二氯喹啉相比,7-氯喹啉4位的-O-戊基和-O-乙基-Cl基团提高了杀幼虫活性。关于[某种蚊虫]的生态毒性研究,生物活性化合物[具体编号]、[具体编号]、[具体编号]和[具体编号]对[某种蚊虫]幼虫显示出中等毒性(LC₅₀ = 101.68 - 314.58 μg·mL⁻¹)。最佳结果表明,化合物[具体编号]可能无致突变性、无肝毒性,且预计不会引起皮肤致敏,对[某种蚊虫]的毒性比对非靶标生物[具体生物名称]高15729倍,是一种更安全的杀幼虫剂。