Evidence map›Paper›PMID 33929818›Full record

ArticleACS infectious diseases2021

Repositioning and Characterization of 1-(Pyridin-4-yl)pyrrolidin-2-one Derivatives as

Masanori Okaniwa, Akira Shibata, Atsuko Ochida, Yuichiro Akao, Karen L White, David M Shackleford, Sandra Duffy, Leonardo Lucantoni, Sumanta Dey, Josefine Striepen and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in ACS infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 14% of its field
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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. New targets for antimalarial drug discovery.Current opinion in microbiology · 2022
    Review
  7. 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

28 authors at 12 institutions in 8 countries.

Masanori OkaniwaTakeda Pharmaceutical Company Limited, 26-1, Muraoka-Higashi 2-chome, Fujisawa, Kanagawa 251-8555, Japan.
Akira ShibataTakeda Pharmaceutical Company Limited, 26-1, Muraoka-Higashi 2-chome, Fujisawa, Kanagawa 251-8555, Japan.
Atsuko OchidaTakeda Pharmaceutical Company Limited, 26-1, Muraoka-Higashi 2-chome, Fujisawa, Kanagawa 251-8555, Japan.
Yuichiro AkaoTakeda Pharmaceutical Company Limited, 26-1, Muraoka-Higashi 2-chome, Fujisawa, Kanagawa 251-8555, Japan.
Karen L WhiteCentre for Drug Candidate Optimisation, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, Victoria 3052, Australia.
David M ShacklefordCentre for Drug Candidate Optimisation, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, Victoria 3052, Australia.
Sandra DuffyDiscovery Biology, Griffith University, Brisbane Innovation Park, Don Young Road, Nathan, Queensland 4111, Australia.
Leonardo LucantoniDiscovery Biology, Griffith University, Brisbane Innovation Park, Don Young Road, Nathan, Queensland 4111, Australia.ORCID 0000-0002-7246-0677
Sumanta DeyDepartment of Biological Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, Massachusetts 02139, United States.
Josefine StriepenDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York 10032, United States.
Tomas YeoDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York 10032, United States.
Sachel MokDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York 10032, United States.ORCID 0000-0002-9605-0154
Anna Caroline C AguiarSao Carlos Institute of Physics, University of São Paulo, Av. João Dagnone, 1100, São Carlos, São Paulo 13563-120, Brazil.
Angelika SturmTropIQ Health Sciences, Transistorweg 5-C02, 6534 AT Nijmegen, The Netherlands.
Benigno CrespoGlobal Health, GlaxoSmithKline R&D, Tres Cantos, Madrid 28760, Spain.
Laura M SanzGlobal Health, GlaxoSmithKline R&D, Tres Cantos, Madrid 28760, Spain.
Alisje ChurchyardDepartment of Life Sciences, Imperial College London, South Kensington, London, SW7 2AZ, United Kingdom.
Jake BaumDepartment of Life Sciences, Imperial College London, South Kensington, London, SW7 2AZ, United Kingdom.
Dhelio B PereiraTropical Medicine Research Center of Rondonia, Av. Guaporé, 215, Porto Velho, Rondonia 76812-329, Brazil.
Rafael V C GuidoSao Carlos Institute of Physics, University of São Paulo, Av. João Dagnone, 1100, São Carlos, São Paulo 13563-120, Brazil.
Koen J DecheringTropIQ Health Sciences, Transistorweg 5-C02, 6534 AT Nijmegen, The Netherlands.
Sergio WittlinSwiss Tropical and Public Health Institute, Socinstrasse 57, 4002 Basel, Switzerland.
Anne-Catrin UhlemannDivision of Infectious Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, New York 10032, United States.
David A FidockDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, New York 10032, United States.
Jacquin C NilesDepartment of Biological Engineering, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, Massachusetts 02139, United States.ORCID 0000-0002-6250-8796
Vicky M AveryDiscovery Biology, Griffith University, Brisbane Innovation Park, Don Young Road, Nathan, Queensland 4111, Australia.
Susan A CharmanCentre for Drug Candidate Optimisation, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, Victoria 3052, Australia.
Benoît LaleuMedicines for Malaria Venture, ICC, Route de Pré-Bois 20, 1215 Geneva, Switzerland.
Columbia University Irving Medical Center · USTakeda (Japan) · JPGriffith University · AUMonash University · AUGlaxoSmithKline (Spain) · ESImperial College London · GBMassachusetts Institute of Technology · USTropIQ Health Sciences · NLUniversidade de São Paulo · BRMedicines for Malaria Venture · CHSwiss Tropical and Public Health Institute · CHUniversidade Federal de Rondônia · BR

Funding

Wellcome TrustWellcome Trust 100993/B/13/Z
6 · The paper itself

Abstract

Prolyl-tRNA synthetase (PRS) is a clinically validated antimalarial target. Screening of a set of PRS ATP-site binders, initially designed for human indications, led to identification of 1-(pyridin-4-yl)pyrrolidin-2-one derivatives representing a novel antimalarial scaffold. Evidence designates cytoplasmic PRS as the drug target. The frontrunner

Indexed as

Amino Acyl-tRNA SynthetasesAntimalarialsMalariaMalaria, FalciparumAnimalsHumansMicePlasmodium falciparumAmino Acyl-tRNA SynthetasesAntimalarialsmalariaPlasmodiumprolyl-tRNA synthetasePRS

Identifiers

PMID33929818
PMCPMC8204304
OpenAlexW3157488875

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.