Evidence map›Paper›PMID 32156719›Full record

ArticleJournal of lipid research2020

Characterization of the small molecule ARC39, a direct and specific inhibitor of acid sphingomyelinase in vitro.

Eyad Naser, Stephanie Kadow, Fabian Schumacher, Zainelabdeen H Mohamed, Christian Kappe, Gabriele Hessler, Barbara Pollmeier, Burkhard Kleuser, Christoph Arenz, Katrin Anne Becker and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

45 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. mBio · 2025
    Article
  8. Article
  9. Article
  10. ThemBio · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Inhibition of the HFrontiers in immunology · 2024
    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 3 countries.

Eyad NaserDepartment of Molecular Biology, University of Duisburg-Essen, 45147 Essen, Germany.
Stephanie KadowDepartment of Molecular Biology, University of Duisburg-Essen, 45147 Essen, Germany.
Fabian SchumacherDepartment of Molecular Biology, University of Duisburg-Essen, 45147 Essen, Germany; Department of Toxicology, Institute of Nutritional Science, University of Potsdam, 14558 Nuthetal, Germany.
Zainelabdeen H MohamedInstitute of Chemistry, Humboldt University of Berlin, 12489 Berlin, Germany; Medicinal Chemistry Department, Faculty of Pharmacy, Assiut University, Assiut 71526, Egypt.
Christian KappeInstitute of Chemistry, Humboldt University of Berlin, 12489 Berlin, Germany.
Gabriele HesslerDepartment of Molecular Biology, University of Duisburg-Essen, 45147 Essen, Germany.
Barbara PollmeierDepartment of Molecular Biology, University of Duisburg-Essen, 45147 Essen, Germany.
Burkhard KleuserDepartment of Toxicology, Institute of Nutritional Science, University of Potsdam, 14558 Nuthetal, Germany.
Christoph ArenzInstitute of Chemistry, Humboldt University of Berlin, 12489 Berlin, Germany.
Katrin Anne BeckerDepartment of Molecular Biology, University of Duisburg-Essen, 45147 Essen, Germany.
Erich GulbinsDepartment of Molecular Biology, University of Duisburg-Essen, 45147 Essen, Germany; Department of Surgery, University of Cincinnati, Cincinnati, OH 45229.
Alexander CarpinteiroDepartment of Molecular Biology, University of Duisburg-Essen, 45147 Essen, Germany; Department of Hematology, University Hospital Essen, 45147 Essen, Germany. Electronic address: mailto:alexander.carpinteiro@uk-essen.de.
University of Duisburg-Essen · DEHumboldt-Universität zu Berlin · DEUniversity of Potsdam · DEEssen University Hospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibition of acid sphingomyelinase (ASM), a lysosomal enzyme that catalyzes the hydrolysis of sphingomyelin into ceramide and phosphorylcholine, may serve as an investigational tool or a therapeutic intervention to control many diseases. Specific ASM inhibitors are currently not sufficiently characterized. Here, we found that 1-aminodecylidene bis-phosphonic acid (ARC39) specifically and efficiently (>90%) inhibits both lysosomal and secretory ASM in vitro. Results from investigating sphingomyelin phosphodiesterase 1 (

Indexed as

Cell LineEnzyme InhibitorsHumansLysosomesSphingomyelin PhosphodiesteraseEnzyme InhibitorsSphingomyelin Phosphodiesterase1-aminodecylidene bis-phosphonic acidacid ceramidasebisphosphonatesceramidesenzymologyfunctional inhibitors of acid sphingomyelinaselipid metabolismlysosomal hydrolaseslysosomesphingolipidssphingomyelin

Identifiers

PMID32156719
PMCPMC7269768
OpenAlexW3011212312

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.