Synthesis and anthelmintic activity of aminochalcones against multiresistant Haemonchus contortus
Matheus Luiggi Freitas Barbosa1, Andreza Pereira Braga1, Karin Vitória Maria Mendonça Ferreira1
1Universidade Estadual do Ceará - UECE, Faculdade de Veterinária, Laboratório de Doenças Parasitárias, Programa de Pós-graduação em Ciências Veterinárias - PPGCV, Fortaleza, CE, Brasil.
None:
The objective of this study was to synthesize and evaluate the in vitro activity of aminochalcones against Haemonchus contortus eggs and adults. Aminochalcones 1 and 2 were synthesized using Claisen-Schmidt condensation and characterized using Fourier-transform infrared spectroscopy, nuclear magnetic resonance, and mass spectrometry. The activity of both aminochalcones was assessed in the egg hatch test and that of aminochalcone 1 was further evaluated in the adult worm motility test using multiresistant H. contortus. The chemical structures of the synthesized compounds were confirmed, and changes induced in eggs and adults were assessed using scanning electron microscopy (SEM). Aminochalcones 1 and 2 inhibited larvae hatching by 98.70 and 99.89%, respectively, at concentrations of 0.25 and 1 mg/mL. SEM images revealed structural and morphological changes in eggs treated with both compounds. After 12 h of exposure to aminochalcone 1 (1.25 mg/mL), all adult nematodes were immobile, and wrinkling of the cuticle was observed. These findings indicate the ovicidal effect of aminochalcones and the inhibition of worm motility by aminochalcone 1. Our preliminary study demonstrated, for the first time, the anthelmintic activity of this class of compounds against gastrointestinal nematodes of small ruminants and suggest further anthelmintic evaluation.
More Related Videos
Related Concept Videos
Cholinergic Antagonists: Chemistry and Structure-Activity Relationship
Indirect-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship
Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...
Anticholinesterase Agents: Poisoning and Treatment
Irreversible agents form a strong bond with the cholinesterase enzyme, making it inactive. The breakdown of the phosphorylated enzyme is...
Indirect-Acting Cholinergic Agonists: Pharmacological Actions
At the neuromuscular junction, these agents work by inhibiting the breakdown of acetylcholine, allowing it to remain bound to the receptor and bind to nearby receptors. This process leads to repetitive firing of the endplate, causing muscle...
Indirect-Acting Cholinergic Agonists: Mechanism of Action
Reversible inhibitors like edrophonium bind to a specific part of the enzyme called the anionic catalytic site. They form noncovalent bonds, which means they are not strongly attached to the enzyme. This creates a temporary and less stable enzyme–inhibitor complex,...
Amines to Sulfonamides: The Hinsberg Test
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing sulfonyl...


