Cargando…
Enhancing diversity in language based models for single-step retrosynthesis
Over the past four years, several research groups demonstrated the combination of domain-specific language representation with recent NLP architectures to accelerate innovation in a wide range of scientific fields. Chemistry is a great example. Among the various chemical challenges addressed with la...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087060/ https://www.ncbi.nlm.nih.gov/pubmed/37065677 http://dx.doi.org/10.1039/d2dd00110a |
_version_ | 1785022264806211584 |
---|---|
author | Toniato, Alessandra Vaucher, Alain C. Schwaller, Philippe Laino, Teodoro |
author_facet | Toniato, Alessandra Vaucher, Alain C. Schwaller, Philippe Laino, Teodoro |
author_sort | Toniato, Alessandra |
collection | PubMed |
description | Over the past four years, several research groups demonstrated the combination of domain-specific language representation with recent NLP architectures to accelerate innovation in a wide range of scientific fields. Chemistry is a great example. Among the various chemical challenges addressed with language models, retrosynthesis demonstrates some of the most distinctive successes and limitations. Single-step retrosynthesis, the task of identifying reactions able to decompose a complex molecule into simpler structures, can be cast as a translation problem, in which a text-based representation of the target molecule is converted into a sequence of possible precursors. A common issue is a lack of diversity in the proposed disconnection strategies. The suggested precursors typically fall in the same reaction family, which limits the exploration of the chemical space. We present a retrosynthesis Transformer model that increases the diversity of the predictions by prepending a classification token to the language representation of the target molecule. At inference, the use of these prompt tokens allows us to steer the model towards different kinds of disconnection strategies. We show that the diversity of the predictions improves consistently, which enables recursive synthesis tools to circumvent dead ends and consequently, suggests synthesis pathways for more complex molecules. |
format | Online Article Text |
id | pubmed-10087060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | RSC |
record_format | MEDLINE/PubMed |
spelling | pubmed-100870602023-04-12 Enhancing diversity in language based models for single-step retrosynthesis Toniato, Alessandra Vaucher, Alain C. Schwaller, Philippe Laino, Teodoro Digit Discov Chemistry Over the past four years, several research groups demonstrated the combination of domain-specific language representation with recent NLP architectures to accelerate innovation in a wide range of scientific fields. Chemistry is a great example. Among the various chemical challenges addressed with language models, retrosynthesis demonstrates some of the most distinctive successes and limitations. Single-step retrosynthesis, the task of identifying reactions able to decompose a complex molecule into simpler structures, can be cast as a translation problem, in which a text-based representation of the target molecule is converted into a sequence of possible precursors. A common issue is a lack of diversity in the proposed disconnection strategies. The suggested precursors typically fall in the same reaction family, which limits the exploration of the chemical space. We present a retrosynthesis Transformer model that increases the diversity of the predictions by prepending a classification token to the language representation of the target molecule. At inference, the use of these prompt tokens allows us to steer the model towards different kinds of disconnection strategies. We show that the diversity of the predictions improves consistently, which enables recursive synthesis tools to circumvent dead ends and consequently, suggests synthesis pathways for more complex molecules. RSC 2023-02-16 /pmc/articles/PMC10087060/ /pubmed/37065677 http://dx.doi.org/10.1039/d2dd00110a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Toniato, Alessandra Vaucher, Alain C. Schwaller, Philippe Laino, Teodoro Enhancing diversity in language based models for single-step retrosynthesis |
title | Enhancing diversity in language based models for single-step retrosynthesis |
title_full | Enhancing diversity in language based models for single-step retrosynthesis |
title_fullStr | Enhancing diversity in language based models for single-step retrosynthesis |
title_full_unstemmed | Enhancing diversity in language based models for single-step retrosynthesis |
title_short | Enhancing diversity in language based models for single-step retrosynthesis |
title_sort | enhancing diversity in language based models for single-step retrosynthesis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087060/ https://www.ncbi.nlm.nih.gov/pubmed/37065677 http://dx.doi.org/10.1039/d2dd00110a |
work_keys_str_mv | AT toniatoalessandra enhancingdiversityinlanguagebasedmodelsforsinglestepretrosynthesis AT vaucheralainc enhancingdiversityinlanguagebasedmodelsforsinglestepretrosynthesis AT schwallerphilippe enhancingdiversityinlanguagebasedmodelsforsinglestepretrosynthesis AT lainoteodoro enhancingdiversityinlanguagebasedmodelsforsinglestepretrosynthesis |