抗寄生虫的
抗寄生虫药
驱虫药
生物
氯离子通道
生物化学
药理学
化学
立体化学
医学
动物
病理
作者
Satish Kumar Rajasekharan,Jin-Hyung Lee,Vinothkannan Ravichandran,Jin‐Cheol Kim,Jae Gyu Park,Jintae Lee
标识
DOI:10.1038/s41598-019-38561-3
摘要
Abstract Parasite death via ion channel activations is the hallmark of anthelmintic and antiparasitic drugs. Glutamate gated chloride channel (GluCl) is a prominent targets for drug selection and design in parasitology. We report several iodine-fluorine based lead activators of GluCl by computational studies and structure-activity relationship analysis. 5-Fluoro-4-iodo-1H-pyrrolo [2, 3-b] pyridine and 5-iodoindole were bioactive hits that displayed in vitro anthelmintic and insecticidal activities against Bursaphelenchus xylophilus , Meloidogyne incognita , and Tenebrio molitor . Two important findings stood out: (i) 5F4IPP induced parasite death, and interacted proficiently with Gln 219 amino acid of pentameric GluCl in docking analysis, and (ii) 5-iodoindole appeared to act by forming giant vacuoles in nematodes, which led to a form of non-apoptotic death known as methuosis. The study suggests halogenated-indoles and 1H-pyrrolo [2, 3-b] pyridine derivatives be regarded potential biocides for plant-parasitic nematodes and insects, and warrants further research on the mode of actions, and field investigations.
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