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A Graph to Graphs Framework for Retrosynthesis Prediction

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A fundamental problem in computational chemistry is to find a set of reactants to synthesize a target molecule, a.k.a. retrosynthesis prediction. Existing state-of-the-art methods rely on matching the target molecule with a large set of reaction templates, which are very computationally expensive and also suffer from the problem of coverage. In this paper, we propose a novel template-free approach called G2Gs by transforming a target molecular graph into a set of reactant molecular graphs. G2Gs first splits the target molecular graph into a set of synthons by identifying the reaction centers, and then translates the synthons to the final reactant graphs via a variational graph translation framework. Experimental results show that G2Gs significantly outperforms existing template-free approaches by up to 63% in terms of the top-1 accuracy and achieves a performance close to that of state-of-the-art template based approaches, but does not require domain knowledge and is much more scalable.

Chence Shi, Minkai Xu, Hongyu Guo, Ming Zhang, Jian Tang• 2020

Related benchmarks

TaskDatasetResultRank
RetrosynthesisUSPTO-50k Reaction type unknown (test)
Top-1 Accuracy48.9
59
RetrosynthesisUSPTO-50k Reaction type known (test)
Top-1 Accuracy61
50
Retrosynthesis predictionUSPTO-50k (test)
Top-1 Accuracy61
39
RetrosynthesisUSPTO-50K
Top-1 Accuracy66.8
33
Retrosynthesis predictionUSPTO-50K
Top-1 Acc (Unknown)48.9
22
Single-step retrosynthesisUSPTO-50k (test)
Top-1 Accuracy48.9
18
RetrosynthesisUSPTO-50K unknown reaction types (test)
Top-1 Accuracy48.9
17
Retrosynthesis (reaction class not given)USPTO-50k (test)
Top-1 Acc48.9
14
Center identificationUSPTO-50K
Top-1 Accuracy90.2
8
Retrosynthesis predictionUSPTO-50k (40/5/5)
Top-1 Accuracy0.489
8
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