Interpretable side reaction detection via atom representations derived from multi-tier reaction perspectives
Recent deep learning-based methods have advanced chemical retrosynthesis. However, they neglect side reactions, strong competitors to desired synthesis reactions that reduce the yield of anticipated product molecules. To identify side-reaction sites, we introduce an atom representation learning framework, SideReact, which explores synthesis reactions from a top-down chemical perspective (i.e., from reaction to motif, to property, and to quantum w.r.t. atoms). Its multi-tier atom encoder (MtAE) extracts top-down observations as atom representations, including reaction paradigms, motif reactivities and co-reactivities, atomic identities and bonding circumstances, and atoms' electron-attracting abilities. Moreover, its hierarchical cross-attention module (HCA) captures the chemical hierarchy among encoding tiers in a bottom-up way. Especially, HCA enables an interpretable path through the hierarchy to reveal how to find reaction sites among atoms in reactants. The comparison with ten state-of-the-art methods demonstrates the superiority of SideReact in both side reactions and desired reactions. Furthermore, a real case study, including ten synthetic examples in textbooks, a complex synthetic reaction of Atorvastatin with side-reaction sites, and a synthetic reaction for a drug-like molecule, substantiates the effectiveness of SideReact. More importantly, analyses demonstrate how its MtAE works and how its HCA unveils the interpretable inference of side-reaction sites, highlighting its potential in retrosynthesis planning.
Authors
- Jian‐Yu Shi (ORCID: https://orcid.org/0000-0002-2303-273X)
- Hui Yu (ORCID: https://orcid.org/0000-0002-5314-8127)
- Haoyang Wang (ORCID: https://orcid.org/0009-0002-1700-5919)
- Jie Shang (ORCID: https://orcid.org/0000-0002-1693-0910)
- Zhen-Yi Wu
- Jia-Ning Li
- Peng-Cheng Zhao
Institutions
- Northwestern Polytechnical University (CN)
Publication Details
- Journal
- Communications Chemistry
- Published
- 2026-11-06
- DOI
- https://doi.org/10.1038/s42004-026-02267-1
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Young Scientists Fund