药物发现
高通量筛选
吞吐量
阿片类药物使用障碍
药品
类阿片
计算机科学
人工智能
医学
药理学
生物信息学
生物
内科学
电信
受体
无线
作者
Xin Hu,Paul Shinn,Zina Itkin,Lin Ye,Ya-Qin Zhang,Min Shen,Stephanie L. Ford‐Scheimer,Matthew D. Hall
标识
DOI:10.1021/acsptsci.4c00256
摘要
As part of the NIH Helping to End Addiction Long-term (HEAL) Initiative, the National Center for Advancing Translational Sciences is dedicated to the development of new pharmacological tools and investigational drugs for managing and treating pain as well as the prevention and treatment of opioid misuse and addiction. In line with these objectives, we created a comprehensive, annotated small molecule library including drugs, probes, and tool compounds that act on published pain- and addiction-relevant targets. Nearly 3000 small molecules associated with approximately 200 known and hypothesized HEAL targets have been assembled, curated, and annotated in one collection. Physical samples of the library compounds have been acquired and plated in 1536-well format, enabling a rapid and efficient high-throughput screen against a wide range of assays. The creation of the HEAL Targets and Compounds Library, coupled with an integrated computational platform for AI-driven machine learning, structural modeling, and virtual screening, provides a valuable source for strategic drug repurposing, innovative profiling, and hypothesis testing of novel targets related to pain and opioid use disorder (OUD). The library is available to investigators for screening pain and OUD-relevant phenotypes.
科研通智能强力驱动
Strongly Powered by AbleSci AI