Leap: molecular synthesisability scoring with intermediates
Not on the map. Why?
Abstract (arXiv)
Assessing whether a molecule can be synthesised is a primary task in drug discovery. It enables computational chemists to filter for viable compounds or bias molecular generative models. The notion of synthesisability is dynamic as it evolves depending on the availability of key compounds. A common approach in drug discovery involves exploring the chemical space surrounding synthetically-accessible intermediates. This strategy improves the synthesisability of the derived molecules due to the availability of key intermediates. Existing synthesisability scoring methods such as SAScore, SCScore and RAScore, cannot condition on intermediates dynamically. Our approach, Leap, is a GPT-2 model trained on the depth, or longest linear path, of predicted synthesis routes that allows information on the availability of key intermediates to be included at inference time. We show that Leap surpasses all other scoring methods by at least 5% on AUC score when identifying synthesisable molecules, and can successfully adapt predicted scores when presented with a relevant intermediate compound.
Key facts. No citing papers in the map yet (data through 7 Oct 2026). Builds on 5 of its 20 references that are in the map. First posted on arXiv 14 Mar 2024.
Builds on
5 of 20 references.
References · 5
- 2018BERT: Pre-training of Deep Bidirectional Transformers for Language Understandingcited by 40,204
- 2018Molecular Transformer - A Model for Uncertainty-Calibrated Chemical Reaction Predictioncited by 225
- 2017Learning to Plan Chemical Synthesescited by 175
- 2020The Synthesizability of Molecules Proposed by Generative Modelscited by 67
- 2021Amortized Tree Generation for Bottom-up Synthesis Planning and Synthesizable Molecular Designcited by 44
Built on by
Not cited yet.