Evidence map›Paper›PMID 38352828›Full record

ArticleACS medicinal chemistry letters2024

Development of Novel Membrane Disrupting Lipoguanidine Compounds Sensitizing Gram-Negative Bacteria to Antibiotics.

Seong-Heun Kim, Charlotte K Hind, Guilherme F S Fernandes, Jingyue Wu, Dorothy Semenya, Melanie Clifford, Caleb Marsh, Silvia Anselmi, A James Mason, Kenneth D Bruce and 2 more

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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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

12 authors.

Seong-Heun KimDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom.
Charlotte K HindAntimicrobial Discovery, Development and Diagnostics, Vaccine Development and Evaluation Centre, UKHSA Porton Down, Salisbury SP4 0JG, United Kingdom.
Guilherme F S FernandesDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom.ORCID https://orcid.org/0000-0002-7644-5466
Jingyue WuDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom.ORCID https://orcid.org/0000-0002-9289-5109
Dorothy SemenyaInstitute of Pharmaceutical Science, School of Cancer & Pharmaceutical Science, King's College London, 150 Stamford Street, London SE1 9NH, United Kingdom.
Melanie CliffordAntimicrobial Discovery, Development and Diagnostics, Vaccine Development and Evaluation Centre, UKHSA Porton Down, Salisbury SP4 0JG, United Kingdom.
Caleb MarshAntimicrobial Discovery, Development and Diagnostics, Vaccine Development and Evaluation Centre, UKHSA Porton Down, Salisbury SP4 0JG, United Kingdom.ORCID https://orcid.org/0000-0002-0265-0221
Silvia AnselmiDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom.
A James MasonInstitute of Pharmaceutical Science, School of Cancer & Pharmaceutical Science, King's College London, 150 Stamford Street, London SE1 9NH, United Kingdom.ORCID https://orcid.org/0000-0003-0411-602X
Kenneth D BruceInstitute of Pharmaceutical Science, School of Cancer & Pharmaceutical Science, King's College London, 150 Stamford Street, London SE1 9NH, United Kingdom.
J Mark SuttonInstitute of Pharmaceutical Science, School of Cancer & Pharmaceutical Science, King's College London, 150 Stamford Street, London SE1 9NH, United Kingdom.
Daniele CastagnoloDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom.ORCID https://orcid.org/0000-0002-7517-5732

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A new class of amphiphilic molecules, the lipoguanidines, designed as hybrids of guanidine and fatty acid compounds, has been synthesized and developed. The new molecules present both a guanidine polar head and a lipophilic tail that allow them to disrupt bacterial membranes and to sensitize Gram-negative bacteria to the action of the narrow-spectrum antibiotics rifampicin and novobiocin. The lipoguanidine

Identifiers

PMID38352828
PMCPMC10860194

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.