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RENATE: A Pseudo‐retrosynthetic Tool for Synthetically Accessible de novo Design
Author(s) -
Ghiandoni Gian Marco,
Bodkin Michael J.,
Chen Beining,
Hristozov Dimitar,
Wallace James E. A.,
Webster James,
Gillet Valerie J.
Publication year - 2022
Publication title -
molecular informatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.481
H-Index - 68
eISSN - 1868-1751
pISSN - 1868-1743
DOI - 10.1002/minf.202100207
Subject(s) - retrosynthetic analysis , computer science , context (archaeology) , heuristics , fragmentation (computing) , combinatorial chemistry , chemistry , programming language , stereochemistry , biology , paleontology , total synthesis , operating system
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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