Title : Synthesis, insecticidal Activity, and molecular docking analysis of some benzo[h]quinoline derivatives against Culex pipiens L. Larvae - El-Helw_2024_Bioorg.Chem_150_107591 |
Author(s) : El-Helw EAE , Hosni EM , Kamal M , Hashem AI , Ramadan SK |
Ref : Bioorg Chem , 150 :107591 , 2024 |
Abstract :
Some heterocycles bearing a benzo[h]quinoline moiety were synthesized through treating a 3-((2-chlorobenzo[h]quinolin-3-yl)methylene)-5-(p-tolyl)furan-2(3H)-one with four nitrogen nucleophiles comprising ammonium acetate, benzylamine, dodecan-1-amine, and 1,2-diaminoethane. Also, thiation reactions of furanone and pyrrolinone derivatives were investigated. The insecticidal activity of these compounds against mosquito larvae (Culex pipiens L.) was evaluated. All tested compounds exhibited significant larvicidal activity, surpassing that of the conventional insecticide chlorpyrifos. In silico docking analysis revealed that these compounds may act as acetyl cholinesterase (AChE) inhibitors, potentially explaining their larvicidal effect. Additionally, interactions with other neuroreceptors, such as nicotinic acetylcholine receptor and sodium channel voltage-gated alpha subunit were also predicted. The results obtained from this study reflected the potential of benzo[h]quinoline derivatives as promising candidates for developing more effective and sustainable mosquito control strategies. The ADME (absorption, distribution, metabolism, and excretion) analyses displayed their desirable drug-likeness and oral bioavailability properties. |
PubMedSearch : El-Helw_2024_Bioorg.Chem_150_107591 |
PubMedID: 38964147 |
El-Helw EAE, Hosni EM, Kamal M, Hashem AI, Ramadan SK (2024)
Synthesis, insecticidal Activity, and molecular docking analysis of some benzo[h]quinoline derivatives against Culex pipiens L. Larvae
Bioorg Chem
150 :107591
El-Helw EAE, Hosni EM, Kamal M, Hashem AI, Ramadan SK (2024)
Bioorg Chem
150 :107591