Evidence map›Paper›PMID 19540764›Full record

ArticleBioorganic & medicinal chemistry2009

Quantitative high-throughput screening identifies inhibitors of anthrax-induced cell death.

Ping Jun Zhu, John P Hobson, Noel Southall, Cunping Qiu, Craig J Thomas, Jiamo Lu, James Inglese, Wei Zheng, Stephen H Leppla, Thomas H Bugge and 2 more

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 33% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. An Aggregation Advisor for Ligand Discovery.Journal of medicinal chemistry · 2015
    Article
  12. Article
  13. Article
  14. Review
  15. Binding interactions of niclosamide with serum proteins.Journal of food and drug analysis · 2014
    Article
  16. Designing inhibitors of anthrax toxin.Expert opinion on drug discovery · 2014
    Review
  17. Article
  18. Article
  19. Article
  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

12 authors at 4 institutions in 1 country.

Ping Jun ZhuNIH Chemical Genomics Center, National Human Genome Research Institute, National Institutes of Health, 9800 Medical Center Drive, Rockville, MD 20850, United States.
John P Hobson
Noel Southall
Cunping Qiu
Craig J Thomas
Jiamo Lu
James Inglese
Wei Zheng
Stephen H Leppla
Thomas H Bugge
Christopher P Austin
Shihui Liu
National Human Genome Research Institute · USNational Institutes of Health · USNational Institute of Allergy and Infectious Diseases · USNational Institute of Dental and Craniofacial Research · US

Funding

Cell surface serine proteases in development, tissue repair, and malignancyZIADE000699 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI BUGGE, THOMAS H · 2009 to 2025
$34.1M
NIH Chemical Genomics CenterZIAHG200319 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI AUSTIN, CHRISTOPHER P · 2009 to 2009
$19.9M
Vaccines and Therapeutics for AnthraxZIAAI000929 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LEPPLA, STEPHEN · 2009 to 2025
$15.9M
Vaccines and Therapeutics for AnthraxZ01AI000929 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI LEPPLA, STEPHEN H · 2003 to 2008
$6.7M
Serine Proteases In Remodeling Of The Extracellular MatrZ01DE000699 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI BUGGE, THOMAS H · 2000 to 2008
$3.2M
Intramural NIH HHS Z01 AI000929Intramural NIH HHS Z01 DE000699Intramural NIH HHS ZIA AI000929Intramural NIH HHS ZIA HG200319
6 · The paper itself

Abstract

Here, we report the results of a quantitative high-throughput screen (qHTS) measuring the endocytosis and translocation of a beta-lactamase-fused-lethal factor and the identification of small molecules capable of obstructing the process of anthrax toxin internalization. Several small molecules protect RAW264.7 macrophages and CHO cells from anthrax lethal toxin and protected cells from an LF-Pseudomonas exotoxin fusion protein and diphtheria toxin. Further efforts demonstrated that these compounds impaired the PA heptamer pre-pore to pore conversion in cells expressing the CMG2 receptor, but not the related TEM8 receptor, indicating that these compounds likely interfere with toxin internalization.

Indexed as

AnimalsAnthraxAnti-Bacterial AgentsAntigens, BacterialBacillus anthracisBacterial ProteinsBacterial ToxinsCell DeathCHO CellsCorynebacterium diphtheriaeCricetinaeCricetulusDiphtheria ToxinEndocytosisExotoxinsMacrophagesanthrax toxinAnti-Bacterial AgentsAntigens, BacterialBacterial ProteinsBacterial ToxinsDiphtheria ToxinExotoxinsSmall Molecule Libraries

Identifiers

PMID19540764
PMCPMC2795356
OpenAlexW2088766721

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.