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RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design
Reaction‐based de novo design refers to the generation of synthetically accessible molecules using transformation rules extracted from known reactions in the literature. In this context, we have previously described the extraction of reaction vectors from a reactions database and their coupling with...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285524/ https://www.ncbi.nlm.nih.gov/pubmed/34750989 http://dx.doi.org/10.1002/minf.202100207 |
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author | Ghiandoni, Gian Marco Bodkin, Michael J. Chen, Beining Hristozov, Dimitar Wallace, James E. A. Webster, James Gillet, Valerie J. |
author_facet | Ghiandoni, Gian Marco Bodkin, Michael J. Chen, Beining Hristozov, Dimitar Wallace, James E. A. Webster, James Gillet, Valerie J. |
author_sort | Ghiandoni, Gian Marco |
collection | PubMed |
description | Reaction‐based de novo design refers to the generation of synthetically accessible molecules using transformation rules extracted from known reactions in the literature. In this context, we have previously described the extraction of reaction vectors from a reactions database and their coupling with a structure generation algorithm for the generation of novel molecules from a starting material. An issue when designing molecules from a starting material is the combinatorial explosion of possible product molecules that can be generated, especially for multistep syntheses. Here, we present the development of RENATE, a reaction‐based de novo design tool, which is based on a pseudo‐retrosynthetic fragmentation of a reference ligand and an inside‐out approach to de novo design. The reference ligand is fragmented; each fragment is used to search for similar fragments as building blocks; the building blocks are combined into products using reaction vectors; and a synthetic route is suggested for each product molecule. The RENATE methodology is presented followed by a retrospective validation to recreate a set of approved drugs. Results show that RENATE can generate very similar or even identical structures to the corresponding input drugs, hence validating the fragmentation, search, and design heuristics implemented in the tool. |
format | Online Article Text |
id | pubmed-9285524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92855242022-07-18 RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design Ghiandoni, Gian Marco Bodkin, Michael J. Chen, Beining Hristozov, Dimitar Wallace, James E. A. Webster, James Gillet, Valerie J. Mol Inform Research Articles Reaction‐based de novo design refers to the generation of synthetically accessible molecules using transformation rules extracted from known reactions in the literature. In this context, we have previously described the extraction of reaction vectors from a reactions database and their coupling with a structure generation algorithm for the generation of novel molecules from a starting material. An issue when designing molecules from a starting material is the combinatorial explosion of possible product molecules that can be generated, especially for multistep syntheses. Here, we present the development of RENATE, a reaction‐based de novo design tool, which is based on a pseudo‐retrosynthetic fragmentation of a reference ligand and an inside‐out approach to de novo design. The reference ligand is fragmented; each fragment is used to search for similar fragments as building blocks; the building blocks are combined into products using reaction vectors; and a synthetic route is suggested for each product molecule. The RENATE methodology is presented followed by a retrospective validation to recreate a set of approved drugs. Results show that RENATE can generate very similar or even identical structures to the corresponding input drugs, hence validating the fragmentation, search, and design heuristics implemented in the tool. John Wiley and Sons Inc. 2021-11-08 2022-04 /pmc/articles/PMC9285524/ /pubmed/34750989 http://dx.doi.org/10.1002/minf.202100207 Text en © 2021 The Authors. Molecular Informatics published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Ghiandoni, Gian Marco Bodkin, Michael J. Chen, Beining Hristozov, Dimitar Wallace, James E. A. Webster, James Gillet, Valerie J. RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design |
title | RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design |
title_full | RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design |
title_fullStr | RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design |
title_full_unstemmed | RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design |
title_short | RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design |
title_sort | renate: a pseudo‐retrosynthetic tool for synthetically accessible de novo design |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285524/ https://www.ncbi.nlm.nih.gov/pubmed/34750989 http://dx.doi.org/10.1002/minf.202100207 |
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