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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.
Afiliação
  • Ghiandoni GM; Information School, University of Sheffield, Regent Court, 211 Portobello, Sheffield, S1 4DP, UK.
  • Bodkin MJ; Evotec (U.K.) Ltd, 114 Innovation Drive Milton Park, Abingdon, OX14 4RZ, UK.
  • Chen B; Chemistry Department, University of Sheffield, Dainton Building, Brook Hill, Sheffield, S3 7HF, UK.
  • Hristozov D; Evotec (U.K.) Ltd, 114 Innovation Drive Milton Park, Abingdon, OX14 4RZ, UK.
  • Wallace JEA; Evotec (U.K.) Ltd, 114 Innovation Drive Milton Park, Abingdon, OX14 4RZ, UK.
  • Webster J; Information School, University of Sheffield, Regent Court, 211 Portobello, Sheffield, S1 4DP, UK.
  • Gillet VJ; Information School, University of Sheffield, Regent Court, 211 Portobello, Sheffield, S1 4DP, UK.
Mol Inform ; 41(4): e2100207, 2022 04.
Article em En | MEDLINE | ID: mdl-34750989
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos Idioma: En Ano de publicação: 2022 Tipo de documento: Article