Kirchner Michael, Marner Michael, Kramer Tim, Mühlemeyer Felix, Eichberg Johanna, Oberpaul Markus, Haeberlein Simone, Göttlich Richard
Institute of Organic Chemistry, Justus Liebig University 35392 Giessen Germany
Branch for Bioresources of the Fraunhofer Institute for Molecular Biology and Applied Ecology 35394 Giessen Germany.
RSC Adv. 2025 Jan 10;15(2):824-831. doi: 10.1039/d4ra05699j. eCollection 2025 Jan 9.
Parasites account for huge economic losses by infecting agriculturally important plants and animals. Furthermore, morbidity and death caused by parasites affect a large part of the world population, especially in economically weak regions. Anthelmintic drugs to tackle this challenge remain scarce and their efficiency becomes increasingly endangered by the advent of drug resistance development. In the present study, we assessed the anthelmintic potential of bis-3-chloropiperidines, a family of compounds which have already demonstrated antiproliferative activity against various cell lines. We synthesized and tested the activity of 21 bis-3-chloropiperidine derivatives against two strains of the free-living nematode (N2 and DC19) and the parasitic flatworm . Overall, bifunctional chloropiperidines featuring an aromatic linker performed best against the tested indicator organisms and could be considered for future optimization efforts. Ultimately, out of the 21 analyzed bis-3-chloropiperidines, four derivatives (2, 5, 9 and 11) reduced vitality parameters against and five the motility of (2, 4, 5, 13, 21) while exhibiting no or low cytotoxicity.
寄生虫通过感染具有重要农业价值的植物和动物造成巨大的经济损失。此外,寄生虫引起的发病和死亡影响着世界上很大一部分人口,尤其是在经济薄弱地区。应对这一挑战的驱虫药物仍然稀缺,而且随着耐药性的出现,其有效性正日益受到威胁。在本研究中,我们评估了双-3-氯哌啶类化合物的驱虫潜力,该类化合物已被证明对多种细胞系具有抗增殖活性。我们合成并测试了21种双-3-氯哌啶衍生物对两种自由生活线虫(N2和DC19)以及寄生扁虫的活性。总体而言,具有芳香族连接基的双功能氯哌啶对测试的指示生物表现最佳,可考虑用于未来的优化工作。最终,在分析的21种双-3-氯哌啶中,四种衍生物(2、5、9和11)降低了对[未提及的某种生物]的活力参数,五种衍生物(2、4、5、13、21)降低了[未提及的某种生物]的运动能力,同时表现出无细胞毒性或低细胞毒性。