Evidence map›Paper›PMID 32112286›Full record

ArticleJournal of computer-aided molecular design2020

Enhancing reaction-based de novo design using a multi-label reaction class recommender.

Gian Marco Ghiandoni, Michael J Bodkin, Beining Chen, Dimitar Hristozov, James E A Wallace, James Webster, Valerie J Gillet

Abstract read
In one paragraph

Article in Journal of computer-aided molecular design, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
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  5. Article
  6. Artificial intelligence in chemistry and drug design.Journal of computer-aided molecular design · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Gian Marco GhiandoniInformation School, University of Sheffield, Regent Court, 211 Portobello, Sheffield, S1 4DP, UK.
Michael J BodkinEvotec (U.K.) Ltd, 114 Innovation Drive, Milton Park, Abingdon, OX14 4RZ, UK.
Beining ChenChemistry Department, University of Sheffield, Dainton Building, Brook Hill, Sheffield, S3 7HF, UK.
Dimitar HristozovEvotec (U.K.) Ltd, 114 Innovation Drive, Milton Park, Abingdon, OX14 4RZ, UK.
James E A WallaceEvotec (U.K.) Ltd, 114 Innovation Drive, Milton Park, Abingdon, OX14 4RZ, UK.
James WebsterInformation School, University of Sheffield, Regent Court, 211 Portobello, Sheffield, S1 4DP, UK.
Valerie J GilletInformation School, University of Sheffield, Regent Court, 211 Portobello, Sheffield, S1 4DP, UK. v.gillet@sheffield.ac.uk.ORCID 0000-0002-8403-3111

Funding

Biotechnology and Biological Sciences Research Council BB/R505821/1
6 · The paper itself

Abstract

Reaction-based de novo design refers to the in-silico generation of novel chemical structures by combining reagents using structural transformations derived from known reactions. The driver for using reaction-based transformations is to increase the likelihood of the designed molecules being synthetically accessible. We have previously described a reaction-based de novo design method based on reaction vectors which are transformation rules that are encoded automatically from reaction databases. A limitation of reaction vectors is that they account for structural changes that occur at the core of a reaction only, and they do not consider the presence of competing functionalities that can compromise the reaction outcome. Here, we present the development of a Reaction Class Recommender to enhance the reaction vector framework. The recommender is intended to be used as a filter on the reaction vectors that are applied during de novo design to reduce the combinatorial explosion of in-silico molecules produced while limiting the generated structures to those which are most likely to be synthesisable. The recommender has been validated using an external data set extracted from the recent medicinal chemistry literature and in two simulated de novo design experiments. Results suggest that the use of the recommender drastically reduces the number of solutions explored by the algorithm while preserving the chance of finding relevant solutions and increasing the global synthetic accessibility of the designed molecules.

Indexed as

Drug DesignAlgorithmsChemistry, PharmaceuticalChemistry Techniques, SyntheticComputer-Aided DesignComputer SimulationDatabases, ChemicalDatabases, PharmaceuticalHumansMachine LearningSmall Molecule LibrariesSmall Molecule LibrariesDe novo designMulti-label classificationReaction class recommenderReaction vector

Identifiers

PMID32112286
PMCPMC7293200

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.