化学
生成语法
人工智能
计算生物学
计算机科学
生成模型
药物发现
自然语言处理
梅德林
限制
作者
Kathryn Giblin,Kun Song,Hongming Chen,Weijie Chen,Zhiqiang Dong,Randolph Escobar,Tyler Grebe,Neil P. Grimster,Alexander W. Hird,Samantha J. Hughes,Jason G. Kettle,Chengzhi Li,Hao Ma,A. Pflug,Magdalena Richter,Marianne Schimpl,Haoran Tang,P P Wang,Gail Wrigley,Ye Wu
标识
DOI:10.1021/acs.jmedchem.6c01048
摘要
Generative artificial intelligence (AI) is now widely applied in medicinal chemistry, with detailed case studies emerging in the literature. Here, we describe an early application of REINVENT, AstraZeneca's in-house generative molecular design platform, to identify new inhibitor scaffolds for hematopoietic progenitor kinase 1 (HPK1). REINVENT was deployed at two stages of the project to address distinct design objectives. For hit identification, transfer learning on kinase-active compounds, followed by reinforcement learning guided by QSAR-based scoring, led to the discovery of three active chemotypes. Subsequently, REINVENT was applied to scaffold hopping, using 3D pharmacophore and docking models as scoring functions, which enabled the identification of two additional active chemotypes. Optimization of one of these scaffolds delivered a compound with potent cellular activity, kinase selectivity, and favorable rat pharmacokinetics. These results demonstrate the value of integrating generative AI with medicinal chemistry expertise and support broader application of the approach in future discovery programs.
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