AI-assisted Retrosynthetic Analysis

Synthetic organic chemistry involves in drug discovery and chemical biology. Retrosynthesis is one of the most complex issues in the field of organic chemistry, which is the design of efficient synthetic routes for a given target. It is an efficient and environmental-friendly synthesis of valuable molecules with well-designed and feasible routes. Evidence show that similar products tend to be produced by similar reactions (Reaxys or SciFinder). For general retrosynthesis planning, a proposed step can come from any reaction class. Key considerations include the need to identify a cascade of disconnections schemes, suitable building blocks and functional group protection strategies. Many additional considerations in synthetic route planning are not limited to cost, process complexity, reaction yield, workup difficulty, safety, and toxicity of intermediates.

Artificial intelligence (AI), driven by improved computing power, data availability and algorithms, underpins chemical drug development. AI-assisted retrosynthetic analysis is starting from the target compound and working backward, which has been well-reviewed over the years. AI approaches have also been reported for prediction of reaction outcomes and optimization of reaction conditions. Potential application of retrosynthetic program may play an important role in de novo molecular design and automated synthesis of molecules.

protheragen AI & MedicineComputer-aided Retrosynthetic Route Planning

The earlier retrosynthesis programs are mainly computer-aided retrosynthetic analysis tools. Template-based methods for retrosynthetic analysis rely on human knowledge of organic synthesis, as well as the encoding of organic and mechanistic rules.

Template-based, rule-based or similarity-based methods

  • protheragen AI & Medicine Confirm the extent of generalization and abstraction.
  • protheragen AI & Medicine Choose reaction databases.
  • protheragen AI & Medicine Encode reaction templates or synthon generation rules.
  • protheragen AI & Medicine Generalize subgraph matching rules (subgraph isomorphism problem).
  • protheragen AI & Medicine Extract the meaningful context around the reaction center.
  • protheragen AI & Medicine Baseline model (Liu et al).
  • protheragen AI & Medicine Synthia (formerly Chematica) developed by Grzybowski and coworkers.
  • protheragen AI & Medicine ReactionPredictor from Baldi's group based on mechanistic views.

Formalized Analysis Workflow Based on Molecular Similarity

Data Set Descriptions of Reaction Classes

Limitations of Template-based Methods

protheragen AI & MedicineAI-assisted Retrosynthesis Planning

Encode chemical reactions as sentences using reaction SMILES in the natural language (NL) framework. Treat forward- or retro- reaction prediction as a translation problem, using different types of neural machine translation architectures.

Transformer-based retrosynthesis (template-free model)

We present a template-free approach that is independent of reaction templates, rules, or atom mapping, to implement automatic retrosynthetic route planning.

Retrosynthetic Route Planning Strategies

protheragen AI & Medicine

Figure 1 Schematic of the Multi-step retrosynthetic workflow. (Philippe Schwaller, et al. 2019)

Evaluation metrics for scalable single-step retrosynthetic models

Workflow

protheragen AI & Medicine

Figure 2 Workflow of Transformer-based Retrosynthesis

In Protheragen, the developed approach mimics the retrosynthetic strategy, which is defined implicitly by a corpus of known reactions without the need to encode any chemical knowledge. We have also tried token- and character-based methods to tokenize the SMILES strings as model input, and used the open-source chemoinformatics software RDKit to validate the model. Protheragen has assessed the entire framework by reviewing several retrosynthetic problems to highlight strengths and weaknesses.

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