Retroformer: Pushing the Limits of Interpretable End-to-end
Retrosynthesis Transformer
- URL: http://arxiv.org/abs/2201.12475v1
- Date: Sat, 29 Jan 2022 02:03:55 GMT
- Title: Retroformer: Pushing the Limits of Interpretable End-to-end
Retrosynthesis Transformer
- Authors: Yue Wan, Benben Liao, Chang-Yu Hsieh, Shengyu Zhang
- Abstract summary: Retrosynthesis prediction is one of the fundamental challenges in organic synthesis.
We propose Retroformer, a novel Transformer-based architecture for retrosynthesis prediction.
Retroformer reaches the new state-of-the-art accuracy for the end-to-end template-free retrosynthesis.
- Score: 15.722719721123054
- License: http://creativecommons.org/licenses/by-nc-sa/4.0/
- Abstract: Retrosynthesis prediction is one of the fundamental challenges in organic
synthesis. The task is to predict the reactants given a core product. With the
advancement of machine learning, computer-aided synthesis planning has gained
increasing interest. Numerous methods were proposed to solve this problem with
different levels of dependency on additional chemical knowledge. In this paper,
we propose Retroformer, a novel Transformer-based architecture for
retrosynthesis prediction without relying on any cheminformatics tools for
molecule editing. Via the proposed local attention head, the model can jointly
encode the molecular sequence and graph, and efficiently exchange information
between the local reactive region and the global reaction context. Retroformer
reaches the new state-of-the-art accuracy for the end-to-end template-free
retrosynthesis, and improves over many strong baselines on better molecule and
reaction validity. In addition, its generative procedure is highly
interpretable and controllable. Overall, Retroformer pushes the limits of the
reaction reasoning ability of deep generative models.
Related papers
- Learning Chemical Reaction Representation with Reactant-Product Alignment [50.28123475356234]
This paper introduces modelname, a novel chemical reaction representation learning model tailored for a variety of organic-reaction-related tasks.
By integrating atomic correspondence between reactants and products, our model discerns the molecular transformations that occur during the reaction, thereby enhancing the comprehension of the reaction mechanism.
We have designed an adapter structure to incorporate reaction conditions into the chemical reaction representation, allowing the model to handle diverse reaction conditions and adapt to various datasets and downstream tasks, e.g., reaction performance prediction.
arXiv Detail & Related papers (2024-11-26T17:41:44Z) - Retro-prob: Retrosynthetic Planning Based on a Probabilistic Model [5.044138778500218]
Retrosynthesis is a fundamental but challenging task in organic chemistry.
Given a target molecule, the goal of retrosynthesis is to find out a series of reactions which could be assembled into a synthetic route.
We propose a new retrosynthetic planning algorithm called retro-prob to maximize the successful synthesis probability of target molecules.
arXiv Detail & Related papers (2024-05-25T08:23:40Z) - UAlign: Pushing the Limit of Template-free Retrosynthesis Prediction with Unsupervised SMILES Alignment [51.49238426241974]
This paper introduces UAlign, a template-free graph-to-sequence pipeline for retrosynthesis prediction.
By combining graph neural networks and Transformers, our method can more effectively leverage the inherent graph structure of molecules.
arXiv Detail & Related papers (2024-03-25T03:23:03Z) - Molecule-Edit Templates for Efficient and Accurate Retrosynthesis
Prediction [0.16070833439280313]
We introduce METRO, a machine-learning model that predicts reactions using minimal templates.
We achieve state-of-the-art results on standard benchmarks.
arXiv Detail & Related papers (2023-10-11T09:00:02Z) - MechRetro is a chemical-mechanism-driven graph learning framework for
interpretable retrosynthesis prediction and pathway planning [10.364476820771607]
MechRetro is a graph learning framework for interpretable retrosynthetic prediction and pathway planning.
By integrating chemical knowledge as prior information, we design a novel Graph Transformer architecture.
We demonstrate that MechRetro outperforms the state-of-the-art approaches for retrosynthetic prediction with a large margin on large-scale benchmark datasets.
arXiv Detail & Related papers (2022-10-06T01:27:53Z) - FusionRetro: Molecule Representation Fusion via In-Context Learning for
Retrosynthetic Planning [58.47265392465442]
Retrosynthetic planning aims to devise a complete multi-step synthetic route from starting materials to a target molecule.
Current strategies use a decoupled approach of single-step retrosynthesis models and search algorithms.
We propose a novel framework that utilizes context information for improved retrosynthetic planning.
arXiv Detail & Related papers (2022-09-30T08:44:58Z) - RetroXpert: Decompose Retrosynthesis Prediction like a Chemist [60.463900712314754]
We devise a novel template-free algorithm for automatic retrosynthetic expansion.
Our method disassembles retrosynthesis into two steps.
While outperforming the state-of-the-art baselines, our model also provides chemically reasonable interpretation.
arXiv Detail & Related papers (2020-11-04T04:35:34Z) - Learning Graph Models for Retrosynthesis Prediction [90.15523831087269]
Retrosynthesis prediction is a fundamental problem in organic synthesis.
This paper introduces a graph-based approach that capitalizes on the idea that the graph topology of precursor molecules is largely unaltered during a chemical reaction.
Our model achieves a top-1 accuracy of $53.7%$, outperforming previous template-free and semi-template-based methods.
arXiv Detail & Related papers (2020-06-12T09:40:42Z) - Retrosynthesis Prediction with Conditional Graph Logic Network [118.70437805407728]
Computer-aided retrosynthesis is finding renewed interest from both chemistry and computer science communities.
We propose a new approach to this task using the Conditional Graph Logic Network, a conditional graphical model built upon graph neural networks.
arXiv Detail & Related papers (2020-01-06T05:36:57Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.