Evidence map›Paper›PMID 28435528›Full record

ArticleACS medicinal chemistry letters2017

Discovery of Highly Selective Inhibitors of the Immunoproteasome Low Molecular Mass Polypeptide 2 (LMP2) Subunit.

Henry W B Johnson, Janet L Anderl, Erin K Bradley, John Bui, Jeffrey Jones, Shirin Arastu-Kapur, Lisa M Kelly, Eric Lowe, David C Moebius, Tony Muchamuel and 3 more

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. [Research progress on selective immunoproteasome inhibitors].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2019
    Review
  13. Article
  14. Article
  15. A Practical Review of Proteasome Pharmacology.Pharmacological reviews · 2019
    Review
  16. Article
  17. The ubiquitin proteasome system as a potential therapeutic target for systemic sclerosis.Translational research : the journal of laboratory and clinical medicine · 2018
    Review
  18. Article
  19. 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

13 authors.

Henry W B JohnsonKezar Life Sciences, 300 Utah Avenue, Suite 105, South San Francisco, California 94080, United States.
Janet L AnderlKezar Life Sciences, 300 Utah Avenue, Suite 105, South San Francisco, California 94080, United States.
Erin K BradleyOnyx Pharmaceuticals, An Amgen Subsidiary, 249 East Grand Avenue, South San Francisco, California 94080, United States.
John BuiOnyx Pharmaceuticals, An Amgen Subsidiary, 249 East Grand Avenue, South San Francisco, California 94080, United States.
Jeffrey JonesOnyx Pharmaceuticals, An Amgen Subsidiary, 249 East Grand Avenue, South San Francisco, California 94080, United States.
Shirin Arastu-KapurOnyx Pharmaceuticals, An Amgen Subsidiary, 249 East Grand Avenue, South San Francisco, California 94080, United States.
Lisa M KellyOnyx Pharmaceuticals, An Amgen Subsidiary, 249 East Grand Avenue, South San Francisco, California 94080, United States.
Eric LoweKezar Life Sciences, 300 Utah Avenue, Suite 105, South San Francisco, California 94080, United States.
David C MoebiusOnyx Pharmaceuticals, An Amgen Subsidiary, 249 East Grand Avenue, South San Francisco, California 94080, United States.
Tony MuchamuelKezar Life Sciences, 300 Utah Avenue, Suite 105, South San Francisco, California 94080, United States.
Christopher KirkKezar Life Sciences, 300 Utah Avenue, Suite 105, South San Francisco, California 94080, United States.
Zhengping WangOnyx Pharmaceuticals, An Amgen Subsidiary, 249 East Grand Avenue, South San Francisco, California 94080, United States.
Dustin McMinnKezar Life Sciences, 300 Utah Avenue, Suite 105, South San Francisco, California 94080, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Building upon the success of bortezomib (VELCADE) and carfilzomib (KYPROLIS), the design of a next generation of inhibitors targeting specific subunits within the immunoproteasome is of interest for the treatment of autoimmune disease. There are three catalytic subunits within the immunoproteasome (low molecular mass polypeptide-7, -2, and multicatalytic endopeptidase complex subunit-1; LMP7, LMP2, and MECL-1), and a campaign was undertaken to design a potent and selective LMP2 inhibitor with sufficient properties to allow for sustained inhibition

Indexed as

constitutive proteasomeimmunoproteasomeLMP2β1cβ1i

Identifiers

PMID28435528
PMCPMC5392757

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.