Evidence map›Paper›PMID 21498685›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Discovery of new antimalarial chemotypes through chemical methodology and library development.

Lauren E Brown, Ken Chih-Chien Cheng, Wan-Guo Wei, Pingwei Yuan, Peng Dai, Richard Trilles, Feng Ni, Jing Yuan, Ryan MacArthur, Rajarshi Guha and 8 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Coinage Metal-Catalyzed Asymmetric Reactions ofMolecules (Basel, Switzerland) · 2022
    Review
  7. Article
  8. Article
  9. Discovery of sultam-containing small-molecule disruptors of the huntingtin-calmodulin protein-protein interaction.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Antiparasitic chemotherapy: from genomes to mechanisms.Annual review of pharmacology and toxicology · 2014
    Review
  20. 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

18 authors at 4 institutions in 1 country.

Lauren E BrownDepartment of Chemistry and Center for Chemical Methodology and Library Development, Boston University, 590 Commonwealth Avenue, Boston, MA 02215.
Ken Chih-Chien Cheng
Wan-Guo Wei
Pingwei Yuan
Peng Dai
Richard Trilles
Feng Ni
Jing Yuan
Ryan MacArthur
Rajarshi Guha
Ronald L Johnson
Xin-zhuan Su
Melissa M Dominguez
John K Snyder
Aaron B Beeler
Scott E Schaus
James Inglese
John A Porco
Boston University · USNational Human Genome Research Institute · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · US

Funding

SYNTHESIS OF LIBRARIES--LINEAR/POLYKETIDE/POLYPROPIONATEP50GM067041 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI PORCO, JOHN A. · 2002 to 2012
$23.7M
Intramural NIH HHSNIGMS NIH HHS P50 GM067041NIGMS NIH HHS P50GM067041
6 · The paper itself

Abstract

In an effort to expand the stereochemical and structural complexity of chemical libraries used in drug discovery, the Center for Chemical Methodology and Library Development at Boston University has established an infrastructure to translate methodologies accessing diverse chemotypes into arrayed libraries for biological evaluation. In a collaborative effort, the NIH Chemical Genomics Center determined IC(50)'s for Plasmodium falciparum viability for each of 2,070 members of the CMLD-BU compound collection using quantitative high-throughput screening across five parasite lines of distinct geographic origin. Three compound classes displaying either differential or comprehensive antimalarial activity across the lines were identified, and the nascent structure activity relationships (SAR) from this experiment used to initiate optimization of these chemotypes for further development.

Indexed as

AntimalarialsHumansMalaria, FalciparumPlasmodium falciparumStructure-Activity RelationshipAntimalarials

Identifiers

PMID21498685
PMCPMC3084078
OpenAlexW2152975479

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.