Evidence map›Paper›PMID 40074291›Full record

ArticleJournal of medicinal chemistry2025

Optimization of Cyclophilin B-Targeted Tri-vector Inhibitors for Novel MASH Treatments.

Maria-Eleni Kouridaki, Jonathan Gillespie, John Robinson, Tanya Mathie, Laura Bain, Duncan McArthur, Angus Morrison, Daniel B Greenslade, Michail Papadourakis, Kasia Maj and 7 more

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2025. 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. Review
  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

17 authors.

Maria-Eleni KouridakiEaStCHEM School of Chemistry, University of Edinburgh, David Brewster Road, Edinburgh, Scotland EH9 3FJ, U.K.
Jonathan GillespieBioAscent Discovery Ltd., Newhouse, Scotland Lanarkshire ML1 5UH, U.K.
John RobinsonBioAscent Discovery Ltd., Newhouse, Scotland Lanarkshire ML1 5UH, U.K.
Tanya MathieBioAscent Discovery Ltd., Newhouse, Scotland Lanarkshire ML1 5UH, U.K.
Laura BainBioAscent Discovery Ltd., Newhouse, Scotland Lanarkshire ML1 5UH, U.K.
Duncan McArthurBioAscent Discovery Ltd., Newhouse, Scotland Lanarkshire ML1 5UH, U.K.
Angus MorrisonBioAscent Discovery Ltd., Newhouse, Scotland Lanarkshire ML1 5UH, U.K.
Daniel B GreensladeEaStCHEM School of Chemistry, University of Edinburgh, David Brewster Road, Edinburgh, Scotland EH9 3FJ, U.K.
Michail PapadourakisEaStCHEM School of Chemistry, University of Edinburgh, David Brewster Road, Edinburgh, Scotland EH9 3FJ, U.K.ORCID 0000-0002-9969-5871
Kasia MajCytochroma Ltd., Roslin Innovation Centre, Easter Bush Estate, Edinburgh, Scotland EH25 9RG, U.K.
Kate CameronCytochroma Ltd., Roslin Innovation Centre, Easter Bush Estate, Edinburgh, Scotland EH25 9RG, U.K.
Darryl TurnerConcept Life Sciences Ltd., Nine, 9 Little France Road, Edinburgh Bioquarter, Edinburgh, Scotland EH16 4UX, U.K.
Scott P WebsterCentre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, 47 Little France Crescent, Edinburgh, Scotland EH16 4TJ, U.K.
Martin A WearThe Edinburgh Protein Production Facility (EPPF), University of Edinburgh, Level 3 Michael Swann Building, King's Buildings, Max Born Crescent, Edinburgh, Scotland EH9 3FF, U.K.
Dahlia Doughty-ShentonCentre for Reproductive Health, Institute for Regeneration and Repair, University of Edinburgh, 4-5 Little France Drive, Edinburgh Bioquarter, Edinburgh, Scotland EH16 4UU, U.K.
Alison N HulmeEaStCHEM School of Chemistry, University of Edinburgh, David Brewster Road, Edinburgh, Scotland EH9 3FJ, U.K.ORCID 0000-0002-4619-1506
Julien MichelEaStCHEM School of Chemistry, University of Edinburgh, David Brewster Road, Edinburgh, Scotland EH9 3FJ, U.K.ORCID 0000-0003-0360-1760

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclophilins have been implicated in the pathophysiology of metabolic dysfunction-associated steatohepatitis (MASH). Pharmacological inhibition of the cyclophilin B isoform has the potential to attenuate liver fibrosis in MASH, but current cyclophilin inhibitors in clinical trials lack isoform selectivity. We previously reported the novel tri-vector small-molecule inhibitor

Indexed as

CyclophilinsAnimalsHumansMaleMiceNon-alcoholic Fatty Liver DiseaseRatsStructure-Activity Relationshipcyclophilin BCyclophilins

Identifiers

PMID40074291
PMCPMC11956012

What Socratic 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 Socratic graph.