Liu Dongping, Liu Dinghao, Sheng Kewei, Cheng Zhenyong, Liu Zixuan, Qiao Yanling, Cai Shangxuan, Li Yulong, Wang Jubo, Chen Hongyang, Hu Chi, Xu Peng, Di Bin, Liao Jun
School of Science, China Pharmaceutical University, Nanjing 211198, China.
Key Laboratory of Drug Monitoring and Control, Drug Intelligence and Forensic Center, Ministry of Public Security, Beijing 100193, China.
Brief Bioinform. 2024 Nov 22;26(1). doi: 10.1093/bib/bbae690.
The supervision of novel psychoactive substances (NPSs) is a global problem, and the regulation of NPSs was heavily relied on identifying structural matches in established NPSs databases. However, violators could circumvent legal oversight by altering the side chain structure of recognized NPSs and the existing methods cannot overcome the inaccuracy and lag of supervision. In this study, we propose a scaffold and transformer-based NPS generation and Screening (STNGS) framework to systematically identify and evaluate potential NPSs. A scaffold-based generative model and a rank function with four parts are contained by our framework. Our generative model shows excellent performance in the design and optimization of general molecules and NPS-like molecules by chemical space analysis and property distribution analysis. The rank function includes synthetic accessibility score and frequency score, as well as confidence score and affinity score evaluated by a neural network, which enables the precise positioning of potential NPSs. Applied STNGS framework with molecular docking and a G protein-coupled receptor (GPCR) activation-based sensor (GRAB), we successfully identify three novel synthetic cannabinoids with activity. STNGS constrains the chemical space to generate NPS-like molecules database with diversity and novelty, which assists in the ex-ante regulation of NPSs.
新型精神活性物质(NPSs)的监管是一个全球性问题,对NPSs的监管严重依赖于在已建立的NPSs数据库中识别结构匹配。然而,违法者可以通过改变已确认NPSs的侧链结构来规避法律监督,而现有方法无法克服监管的不准确和滞后性。在本研究中,我们提出了一种基于支架和变换器的NPS生成与筛选(STNGS)框架,以系统地识别和评估潜在的NPSs。我们的框架包含一个基于支架的生成模型和一个由四部分组成的排序函数。我们的生成模型通过化学空间分析和性质分布分析,在一般分子和类NPS分子的设计和优化中表现出优异的性能。排序函数包括合成可及性得分和频率得分,以及通过神经网络评估的置信度得分和亲和力得分,这使得能够精确定位潜在的NPSs。将STNGS框架应用于分子对接和基于G蛋白偶联受体(GPCR)激活的传感器(GRAB),我们成功鉴定出三种具有活性的新型合成大麻素。STNGS限制化学空间以生成具有多样性和新颖性的类NPS分子数据库,这有助于对NPSs进行事前监管。