Evidence map›Paper›PMID 37974949›Full record

ArticleACS medicinal chemistry letters2023

Design of Novel Series of Antimalarial PMX Inhibitors with Increased Half-Life via Molecular Property Optimization.

Komei Sakata, Martin A Lowe, Mengyang Xuan, Jeffrey Bruffaerts, Luigi P Stasi, Bénédicte Lallemand, Alvaro Cardenas, Richard D Taylor, Lewis R Vidler, Lloyd King and 3 more

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

13 authors.

Komei SakataUCB, 216 Bath Road, Slough SL1 3WE, United Kingdom.
Martin A LoweUCB, 216 Bath Road, Slough SL1 3WE, United Kingdom.
Mengyang XuanUCB, 216 Bath Road, Slough SL1 3WE, United Kingdom.
Jeffrey BruffaertsUCB, 216 Bath Road, Slough SL1 3WE, United Kingdom.
Luigi P StasiUCB, 216 Bath Road, Slough SL1 3WE, United Kingdom.
Bénédicte LallemandUCB, Chem. du Foriest 1, 1420 Braine-l'Alleud, Belgium.
Alvaro CardenasUCB, Chem. du Foriest 1, 1420 Braine-l'Alleud, Belgium.
Richard D TaylorUCB, 216 Bath Road, Slough SL1 3WE, United Kingdom.ORCID https://orcid.org/0000-0002-4808-5010
Lewis R VidlerUCB, 216 Bath Road, Slough SL1 3WE, United Kingdom.
Lloyd KingUCB, 216 Bath Road, Slough SL1 3WE, United Kingdom.
Jean-Pierre ValentinUCB, Chem. du Foriest 1, 1420 Braine-l'Alleud, Belgium.
Benoît LaleuMedicines for Malaria Venture, ICC, Route de Pré-Bois 20, 1215 Geneva, Switzerland.ORCID https://orcid.org/0000-0002-7530-2113
Teresa de HaroUCB, Chem. du Foriest 1, 1420 Braine-l'Alleud, Belgium.ORCID https://orcid.org/0000-0002-6860-3970

Funding

Wellcome Trust
6 · The paper itself

Abstract

Plasmepsin X (PMX) has been identified as a multistage antimalarial target. PMX is a malarial aspartyl protease essential for merozoite egress from infected red blood cells and invasion of the host erythrocytes. Previously, we reported the identification of PMX inhibitors by structure-based optimization of a cyclic guanidine core. Preclinical assessment of

Identifiers

PMID37974949
PMCPMC10641918

What OpenQuestion holds

Textmetadata
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.