Evidence map›Paper›PMID 31836637›Full record

ArticleMolecular & cellular proteomics : MCP2020

Multi-omic Characterization of the Mode of Action of a Potent New Antimalarial Compound, JPC-3210, Against

Geoffrey W Birrell, Matthew P Challis, Amanda De Paoli, Dovile Anderson, Shane M Devine, Gavin D Heffernan, David P Jacobus, Michael D Edstein, Ghizal Siddiqui, Darren J Creek

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Real-time measurements of ATP dynamics via ATeams inAntimicrobial agents and chemotherapy · 2024
    Article
  7. Origins, Technological Advancement, and Applications of Peptidomics.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  8. Review
  9. Current and emerging target identification methods for novel antimalarials.International journal for parasitology. Drugs and drug resistance · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Targeting malaria parasites with novel derivatives of azithromycin.Frontiers in cellular and infection microbiology · 2022
    Article
  14. Methods Used to Investigate theFrontiers in cellular and infection microbiology · 2021
    Review
  15. 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

10 authors at 2 institutions in 2 countries.

Geoffrey W BirrellAustralian Defense Force Malaria and Infectious Disease Institute, Brisbane, Australia.
Matthew P ChallisMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, Australia.
Amanda De PaoliMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, Australia.
Dovile AndersonMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, Australia.
Shane M DevineMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, Australia.
Gavin D HeffernanJacobus Pharmaceutical Company, Plainsboro, New Jersey.
David P JacobusJacobus Pharmaceutical Company, Plainsboro, New Jersey.
Michael D EdsteinAustralian Defense Force Malaria and Infectious Disease Institute, Brisbane, Australia.
Ghizal SiddiquiMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, Australia. Electronic address: Ghizal.siddiqui@monash.edu.
Darren J CreekMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, Australia.
Monash University · AUSustainable Development Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing incidence of antimalarial drug resistance to the first-line artemisinin combination therapies underpins an urgent need for new antimalarial drugs, ideally with a novel mode of action. The recently developed 2-aminomethylphenol, JPC-3210, (MMV 892646) is an erythrocytic schizonticide with potent

Indexed as

AntimalarialsHemoglobinsMetabolomicsPeptidesPhenolsPlasmodium falciparumProteomicsProtozoan ProteinsAntimalarialsHemoglobinsJPC-3210PeptidesPhenolsProtozoan Proteins2-aminomethylphenolantimalarial drug discoverydrug targetsmalariametabolitesMetabolomicsmode of actionpeptidomicsproteomics

Identifiers

PMID31836637
PMCPMC7000111
OpenAlexW2995846894

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.