Evidence map›Paper›PMID 36214647›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2023

Dithiolopyrrolones are Prochelators that are Activated by Glutathione.

Francesca Albini, Stefan Bormann, Philipp Gerschel, Veza A Ludwig, Wilma Neumann

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Dithiolopyrrolones are Prochelators that are Activated by Glutathione.Chemistry (Weinheim an der Bergstrasse, Germany) · 2023
    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

5 authors.

Francesca AlbiniInorganic Chemistry I - Bioinorganic Chemistry, Ruhr-University Bochum, 44780, Bochum, Germany.
Stefan BormannInorganic Chemistry I - Bioinorganic Chemistry, Ruhr-University Bochum, 44780, Bochum, Germany.
Philipp GerschelInorganic Chemistry I - Bioinorganic Chemistry, Ruhr-University Bochum, 44780, Bochum, Germany.
Veza A LudwigInorganic Chemistry I - Bioinorganic Chemistry, Ruhr-University Bochum, 44780, Bochum, Germany.
Wilma NeumannInorganic Chemistry I - Bioinorganic Chemistry, Ruhr-University Bochum, 44780, Bochum, Germany.ORCID http://orcid.org/0000-0002-1728-5140

Funding

Fonds der Chemischen Industrie
6 · The paper itself

Abstract

Dithiolopyrrolones (DTPs), such as holomycin, are natural products that hold promise as scaffolds for antibiotics as they exhibit inhibitory activity against antibiotic-resistant pathogens. They consist of a unique bicyclic core containing a disulfide that is crucial for their biological activity. Herein, we establish the DTPs as prochelators. We show that the disulfides are reduced at cellular gluathione levels. This activates the drugs and initiates interactions with targets, particularly metal coordination. In addition, we report an expedient synthesis for the DTPs thiolutin and aureothricin, providing facile access to important natural DTPs and derivatives thereof.

Indexed as

Anti-Bacterial AgentsMetalsDisulfidesGlutathionePyrrolesSulfhydryl CompoundsAnti-Bacterial AgentsDisulfidesGlutathioneMetalsPyrrolesSulfhydryl CompoundsAntibioticsantitumor agentsdisulfidenatural productsprodrugs

Identifiers

PMID36214647
PMCPMC10099403

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.