Evidence map›Paper›PMID 28983993›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2017

Synthesis and Demonstration of the Biological Relevance of sp

Daniel J Foley, Philip G E Craven, Patrick M Collins, Richard G Doveston, Anthony Aimon, Romain Talon, Ian Churcher, Frank von Delft, Stephen P Marsden, Adam Nelson

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Harnessing COJournal of the American Chemical Society · 2026
    Article
  2. Article
  3. Article
  4. Aryl Acid-Alcohol Cross-Coupling: C(spJournal of the American Chemical Society · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Scaffold Remodelling of Diazaspirotricycles Enables Synthesis of Diverse spChemistry (Weinheim an der Bergstrasse, Germany) · 2023
    Article
  10. Article
  11. Article
  12. A GeneralChem · 2021
    Article
  13. Review
  14. Article
  15. Phenotyping Reveals Targets of a Pseudo-Natural-Product Autophagy Inhibitor.Angewandte Chemie (International ed. in English) · 2020
    Article
  16. Article
  17. Review
  18. Readily accessible spChemical science · 2020
    Article
  19. Article
  20. Structure-guided fragment-based drug discovery at the synchrotron: screening binding sites and correlations with hotspot mapping.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2019
    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

10 authors.

Daniel J FoleyAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0001-6221-3333
Philip G E CravenAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0002-7617-132X
Patrick M CollinsDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot, OX11 0QX, UK.
Richard G DovestonAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0002-7399-9607
Anthony AimonAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.
Romain TalonStructural Genomics Consortium, Nuffield Department of Medicine, University of Oxford, Roosevelt Drive, Oxford, OX3 7DQ, UK.
Ian ChurcherGlaxoSmithKline Medicines Research Centre, Stevenage, SG1 2NY, UK,BenevolentBio, Churchway, London, NW1 1LW, UK.
Frank von DelftDiamond Light Source Ltd, Harwell Science and Innovation Campus, Didcot, OX11 0QX, UK.ORCID http://orcid.org/0000-0003-0378-0017
Stephen P MarsdenSchool of Chemistry, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0002-4976-7531
Adam NelsonAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0003-3886-363X

Funding

Wellcome Trust
6 · The paper itself

Abstract

The productive exploration of chemical space is an enduring challenge in chemical biology and medicinal chemistry. Natural products are biologically relevant, and their frameworks have facilitated chemical tool and drug discovery. A "top-down" synthetic approach is described that enabled a range of complex bridged intermediates to be converted with high step efficiency into 26 diverse sp

Indexed as

ATPases Associated with Diverse Cellular ActivitiesBinding SitesBiological ProductsBromodomain Containing ProteinsCatalytic DomainDNA-Binding ProteinsHigh-Throughput Screening AssaysHistone AcetyltransferasesHistone ChaperonesHumansJumonji Domain-Containing Histone DemethylasesLigandsMolecular Docking SimulationNuclear ProteinsProtein DomainsQuantum TheoryATAD2 protein, humanATPases Associated with Diverse Cellular ActivitiesBiological ProductsBRD1 protein, humanBromodomain Containing ProteinsDNA-Binding ProteinsHistone AcetyltransferasesHistone ChaperonesJumonji Domain-Containing Histone DemethylasesKDM4D protein, humanLigandsNuclear ProteinsSmall Molecule Librarieschemical biologyfragmentsmolecular diversitynatural productsproteins

Identifiers

PMID28983993
PMCPMC5703167

What OpenQuestion holds

Textmetadata
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.