Evidence map›Paper›PMID 41816614›Full record

ArticleChemical science2026

Amino acid appended supramolecular self-associating amphiphiles demonstrate dual activity against both MRSA and ovarian cancer.

Precious I A Popoola, Thomas L Allam, Rebecca J Lilley, Chandni Manwani, Olivia B Keers, Junyang Tan, Kylie Yang, Yifan Long, Ewan R Clark, Lisa J White and 14 more

Abstract read
In one paragraph

Article in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

24 authors.

Precious I A PopoolaUniversity of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk M.D.Garrett@kent.ac.uk.ORCID https://orcid.org/0000-0002-3961-3782
Thomas L AllamSchool of Chemistry, University of Southampton Highfield Southampton SO17 1BJ UK.ORCID https://orcid.org/0009-0009-9897-333X
Rebecca J LilleyUniversity of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk M.D.Garrett@kent.ac.uk.
Chandni ManwaniUniversity of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk M.D.Garrett@kent.ac.uk.ORCID https://orcid.org/0000-0002-5068-2527
Olivia B KeersUniversity of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk M.D.Garrett@kent.ac.uk.
Junyang TanChemistry Department, UCL 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.
Kylie YangChemistry Department, UCL 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.ORCID https://orcid.org/0000-0002-4455-3681
Yifan LongChemistry Department, UCL 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.
Ewan R ClarkSchool of Science, University of Greenwich Chatham Maritime Kent ME4 4TB UK.
Lisa J WhiteUniversity of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk M.D.Garrett@kent.ac.uk.
Kira L F HiltonUniversity of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk M.D.Garrett@kent.ac.uk.
Jennifer RankinCancer Research Horizons, Babraham Research Campus Cambridge CB22 3AT UK.
Jennifer BakerCancer Research Horizons, Babraham Research Campus Cambridge CB22 3AT UK.ORCID https://orcid.org/0009-0008-1290-7845
Charlotte BennettCancer Research Horizons, Babraham Research Campus Cambridge CB22 3AT UK.
Hollie B WilsonCancer Research Horizons, Babraham Research Campus Cambridge CB22 3AT UK.
Evelyn R MortonChemistry Department, UCL 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.
Alvaro KeskkülaChemistry Department, UCL 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.
Bethany MartinResearch and Evaluation, Porton Down, UKHSA Salisbury SP4 0JG UK Charlotte.Hind@UKHSA.gov.uk.
Christopher O'ConnorResearch and Evaluation, Porton Down, UKHSA Salisbury SP4 0JG UK Charlotte.Hind@UKHSA.gov.uk.ORCID https://orcid.org/0009-0005-6429-4620
J Mark SuttonResearch and Evaluation, Porton Down, UKHSA Salisbury SP4 0JG UK Charlotte.Hind@UKHSA.gov.uk.
Charlotte K HindResearch and Evaluation, Porton Down, UKHSA Salisbury SP4 0JG UK Charlotte.Hind@UKHSA.gov.uk.
Michelle D GarrettUniversity of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk M.D.Garrett@kent.ac.uk.
Cally J E HaynesChemistry Department, UCL 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.ORCID https://orcid.org/0000-0003-4262-8560
Jennifer R HiscockUniversity of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk M.D.Garrett@kent.ac.uk.ORCID https://orcid.org/0000-0002-1406-8802

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differences in the lipid composition of prokaryotic and eukaryotic cell membranes are well understood and can be exploited to produce novel antimicrobials. However, what is less well recognised is that alteration in the phospholipid composition of the cell membrane is also one of the first phenotypic changes when a cell becomes cancerous. In addition, changes in phospholipid cell membrane composition are a known cause of drug resistance in both microbial disease and cancer. Here we present a novel, next generation series of chiral, amino acid appended supramolecular self-associating amphiphiles that suggest membrane active technologies can be used to produce novel drugs which simultaneously fight against two of the greatest global health threats facing us today, antimicrobial resistant infections and cancer diseases. We demonstrate the antimicrobial and anticancer efficacy of this membrane active amphiphile technology against susceptible and resistant

Identifiers

PMID41816614
PMCPMC12973313

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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.