Evidence map›Paper›PMID 34094174›Full record

ArticleChemical science2020

The dark side of disulfide-based dynamic combinatorial chemistry.

Mélissa Dumartin, Jean Septavaux, Marion Donnier-Maréchal, Emeric Jeamet, Elise Dumont, Florent Perret, Laurent Vial, Julien Leclaire

Abstract read
In one paragraph

Article in Chemical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. COACS omega · 2026
    Article
  2. Article
  3. Article
  4. Dynamic Nucleophilic Aromatic Substitution of Tetrazines.Angewandte Chemie (International ed. in English) · 2021
    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

8 authors.

Mélissa DumartinUniv. Lyon, Univ. Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France florent.perret@univ-lyon1.fr laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.ORCID https://orcid.org/0000-0002-9924-3031
Jean SeptavauxUniv. Lyon, Univ. Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France florent.perret@univ-lyon1.fr laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.ORCID https://orcid.org/0000-0002-0134-3086
Marion Donnier-MaréchalUniv. Lyon, Univ. Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France florent.perret@univ-lyon1.fr laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.
Emeric JeametUniv. Lyon, Univ. Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France florent.perret@univ-lyon1.fr laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.
Elise DumontENS Lyon, Univ. Lyon 1, CNRS, Laboratoire de Chimie F-69364 France.ORCID https://orcid.org/0000-0002-2359-111X
Florent PerretUniv. Lyon, Univ. Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France florent.perret@univ-lyon1.fr laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.ORCID https://orcid.org/0000-0003-1413-6374
Laurent VialUniv. Lyon, Univ. Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France florent.perret@univ-lyon1.fr laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.ORCID https://orcid.org/0000-0002-0357-0573
Julien LeclaireUniv. Lyon, Univ. Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France florent.perret@univ-lyon1.fr laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.ORCID https://orcid.org/0000-0001-7984-9055

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the last two decades, disulfide-based dynamic combinatorial chemistry has been extensively used in the field of molecular recognition to deliver artificial receptors for molecules of biological interest. Commonly, the nature of library members and their relative amounts are provided from HPLC-MS analysis of the libraries, allowing the identification of potential binders for a target (bio)molecule. By re-investigating dynamic combinatorial libraries generated from a simple 2,5-dicarboxy-1,4-dithiophenol building block in water, we herein demonstrated that multiple analytical tools were actually necessary in order to comprehensively describe the libraries in terms of size, stereochemistry, affinity, selectivity, and finally to get a true grasp on the different phenomena at work within dynamic combinatorial systems.

Identifiers

PMID34094174
PMCPMC8163284

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Registered trials

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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.