首页> 外文OA文献 >Screening of the 'Open Scaffolds' collection from Compounds Australia identifies a new chemical entity with anthelmintic activities against different developmental stages of the barber's pole worm and other parasitic nematodes
【2h】

Screening of the 'Open Scaffolds' collection from Compounds Australia identifies a new chemical entity with anthelmintic activities against different developmental stages of the barber's pole worm and other parasitic nematodes

机译:来自Compounds australia的'Open scaffolds'系列的筛选确定了一种新的化学实体,具有驱虫活性,可以对抗理发师的极虫和其他寄生线虫的不同发育阶段

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The discovery and development of novel anthelmintic classes is essential to sustain the control of socioeconomically important parasitic worms of humans and animals. With the aim of offering novel, lead-like scaffolds for drug discovery, Compounds Australia released the 'Open Scaffolds' collection containing 33,999 compounds, with extensive information available on the physicochemical properties of these chemicals. In the present study, we screened 14,464 prioritised compounds from the 'Open Scaffolds' collection against the exsheathed third-stage larvae (xL3s) of Haemonchus contortus using recently developed whole-organism screening assays. We identified a hit compound, called SN00797439, which was shown to reproducibly reduce xL3 motility by ≥ 70%; this compound induced a characteristic, "coiled" xL3 phenotype (IC50 = 3.46-5.93 μM), inhibited motility of fourth-stage larvae (L4s; IC50 = 0.31-12.5 μM) and caused considerable cuticular damage to L4s in vitro. When tested on other parasitic nematodes in vitro, SN00797439 was shown to inhibit (IC50 = 3-50 μM) adults of Ancylostoma ceylanicum (hookworm) and first-stage larvae of Trichuris muris (whipworm) and eventually kill (>90%) these stages. Furthermore, this compound completely inhibited the motility of female and male adults of Brugia malayi (50-100 μM) as well as microfilariae of both B. malayi and Dirofilaria immitis (heartworm). Overall, these results show that SN00797439 acts against genetically (evolutionarily) distant parasitic nematodes i.e. H. contortus and A. ceylanicum [strongyloids] vs. B. malayi and D. immitis [filarioids] vs. T. muris [enoplid], and, thus, might offer a novel, lead-like scaffold for the development of a relatively broad-spectrum anthelmintic. Our future work will focus on assessing the activity of SN00797439 against other pathogens that cause neglected tropical diseases, optimising analogs with improved biological activities and characterising their targets.
机译:新型驱虫类的发现和发展对于维持对人类和动物具有社会经济意义的寄生虫的控制至关重要。为了提供用于药物发现的新颖的铅样支架,澳大利亚化合物协会发布了“开放支架”系列,其中包含33,999种化合物,并提供了有关这些化学物质的理化性质的大量信息。在本研究中,我们使用最近开发的全生物筛选测定法,从“开放式脚手架”中筛选了14 464个优先化合物,这些化合物针对的是捻转的Haemonchus contortus的第三阶段幼虫(xL3s)。我们确定了一种名为SN00797439的命中化合物,该化合物可再现地将xL3活力降低≥70%;该化合物诱导出特征性的``螺旋''xL3表型(IC50 =3.46-5.93μM),抑制了第四阶段幼虫的活力(L4s; IC50 =0.31-12.5μM),并在体外对L4s造成了严重的表皮损伤。当在体外对其他寄生线虫进行测试时,表明SN00797439可抑制(IC50 = 3-50μM)成年成虫成虫(钩虫)和Trichuris muris的第一阶段幼虫(鞭虫)并最终杀死(> 90%)这些阶段。此外,该化合物完全抑制了马来布鲁吉虫(Brugia malayi)(50-100μM)的雌性和雄性成虫的活力以及马来芽胞杆菌和Dirofilaria炎(心丝虫)的微丝aria。总体而言,这些结果表明,SN00797439对遗传上(进化上)较远的寄生线虫起作用,即H. contortus和A. ceanianicum [strongyloids] vs. B. malayi和D. Immitis [filarioids] vs. T. muris [enoplid],以及,因此,可能为开发相对广谱的驱虫药提供一种新颖的,类似铅的支架。我们未来的工作将集中在评估SN00797439对引起其他被忽视的热带病的病原体的活性,优化具有改善的生物活性的类似物以及表征其靶标。

相似文献

  • 外文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号