环加成
工作流程
点击化学
反应性(心理学)
计算机科学
化学
计算化学
量子化学
标杆管理
反应机理
组合化学
计算科学
生化工程
有机化学
数据库
催化作用
业务
病理
营销
工程类
替代医学
医学
作者
Thijs Stuyver,Kjell Jorner,Connor W. Coley
出处
期刊:Scientific Data
[Nature Portfolio]
日期:2023-02-01
卷期号:10 (1): 66-66
被引量:52
标识
DOI:10.1038/s41597-023-01977-8
摘要
Bio-orthogonal click chemistry based on [3 + 2] dipolar cycloadditions has had a profound impact on the field of biochemistry and significant effort has been devoted to identify promising new candidate reactions for this purpose. To gauge whether a prospective reaction could be a suitable bio-orthogonal click reaction, information about both on- and off-target activation and reaction energies is highly valuable. Here, we use an automated workflow, based on the autodE program, to compute over 5000 reaction profiles for [3 + 2] cycloadditions involving both synthetic dipolarophiles and a set of biologically-inspired structural motifs. Based on a succinct benchmarking study, the B3LYP-D3(BJ)/def2-TZVP//B3LYP-D3(BJ)/def2-SVP level of theory was selected for the DFT calculations, and standard conditions and an (aqueous) SMD model were imposed to mimic physiological conditions. We believe that this data, as well as the presented workflow for high-throughput reaction profile computation, will be useful to screen for new bio-orthogonal reactions, as well as for the development of novel machine learning models for the prediction of chemical reactivity more broadly.
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