...
首页> 外文期刊>Current drug discovery technologies >Application of the In Combo Screening Approach For the Discovery of Non-Alkaloid Acetylcholinesterase Inhibitors from Cichorium intybus
【24h】

Application of the In Combo Screening Approach For the Discovery of Non-Alkaloid Acetylcholinesterase Inhibitors from Cichorium intybus

机译:组合筛选方法在菊苣中发现非生物碱乙酰胆碱酯酶抑制剂中的应用

获取原文
获取原文并翻译 | 示例

摘要

Because of the direct correlation of cholinergic deficit and the severity of dementia, Alzheimer's disease is preferentially treated with acetylcholinesterase (AChE) inhibitors to supplement the acetylcholine level. In this study we focused on non-alkaloid AChE inhibitors from natural sources in order to discover new lead structures.In the course of in vitro extract screening of Tyrolean plants using an enzyme assay with Ellman's reagent, the dichloromethane extract of chicory roots (Cichorium intybus L.) showed a pronounced inhibitory effect on AChE. At a concentration of 1 mg extract/ml an inhibition of 70% was measured. Based on a 3D multi-conformational molecular-structure database consisting of secondary metabolites from C. intybus known from the relevant literature, virtual screening filtering experiments were conducted using both a feature-based pharmacophore model and a docking procedure. Some low molecular w,eight sesquiterpenoids exhibited distinct interactions with the pharmacophore model.In order to verify the applicability of this computer-aided strategy, an activity-guided fractionation of the chicory root extract was performed, which resulted in the isolation of two sesquiterpene lactones, 8-deoxylactucin and lactucopicrin, showing significant and dose-dependent inhibitory activity on AChE (IC_50 of 308.1 uM [CI95 243.9 - 405.3 uM] and 150.3 uM [Cl_95 100.8 - 188.1 uM], respectively). The two isolates were correctly predicted within the virtual screening process which corroborates the potential of the computer-assisted in combo screening approach for the discovery of the anti-cholinesterase compounds from C. intybus.
机译:由于胆碱能缺乏症和痴呆症的严重程度直接相关,因此优先采用乙酰胆碱酯酶(AChE)抑制剂治疗阿尔茨海默氏病,以补充乙酰胆碱水平。在这项研究中,我们集中于天然来源的非生物碱AChE抑制剂,以发现新的先导结构。在使用Ellman试剂进行酶测定的提洛尔植物体外提取物筛选过程中,菊苣根的二氯甲烷提取物(菊苣(Cichorium intybus) L.)对AChE表现出明显的抑制作用。在1 mg提取物/ ml的浓度下,测得的抑制率为70%。基于由相关文献中已知的隐孢子虫次生代谢物组成的3D多构象分子结构数据库,使用基于特征的药效团模型和对接程序进行了虚拟筛选过滤实验。一些低分子量,八倍的倍半萜类化合物与药效团模型表现出独特的相互作用。 ,8-脱氧乳球菌素和乳杆菌苦蛋白对AChE表现出显着的剂量依赖性抑制作用(IC_50分别为308.1 uM [CI95 243.9-405.3 uM]和150.3 uM [Cl_95 100.8-188.1 uM])。在虚拟筛选过程中正确预测了这两个分离株,这证实了计算机辅助的组合筛选方法从隐孢子虫中发现抗胆碱酯酶化合物的潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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