...
首页> 外文期刊>Journal of Proteins and Proteomics >Identification of effective and specific serotonin1B receptor ligands by structure-based virtual screening and molecular dynamics
【24h】

Identification of effective and specific serotonin1B receptor ligands by structure-based virtual screening and molecular dynamics

机译:

获取原文
获取原文并翻译 | 示例
           

摘要

The serotonergic systems are the most important therapeutic targets for neurological disorders. Many serotonergic drugs have been used to treat neurological disorders, which are well known for their adverse side effects because of the off-target interactions. Development of selective ligands for a specific target is the suitable approach to minimize the off-target interactions and side effects. To identify selective ligands for serotonin 1B receptor (5-HT 1B R), the structural analogs of inverse agonist methiothepin (MT) and natural products were screened against 5-HT 1B R and other 5-HTR subtypes (5-HT 2A R, 5-HT 2B R, and 5-HT 2C R). In the present study, five compounds were selected out of 9963 screened compounds having higher binding affinity with 5-HT 1B R over other 5-HTRs. Amongst them, ZINC31166967 and ZINC31162553 exhibited relatively higher binding affinity towards 5-HT 1B R with the binding energy of − 10.1 and − 9.1 kcal/mol, respectively. The pharmacokinetic assessments considered them safe and non-toxic. Molecular dynamics (MD) simulation revealed the stability of these compounds within the active site of the receptor. The overall analysis suggested that ZINC31166967 and ZINC31162553 may be considered as the selective ligands for 5-HT 1B R. However, detailed experimental investigations will be required to substantiate the findings.

著录项

相似文献

  • 外文文献
  • 中文文献
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