Evidence map›Paper›PMID 36608337›Full record

ArticleJournal of medicinal chemistry2023

Discovery of Highly Selective Inhibitors of the Human Constitutive Proteasome β5c Chymotryptic Subunit.

Wenhu Zhan, Daqiang Li, Priya Saha, Rong Wang, Hao Zhang, Amrendra K Ajay, Christa Deban, George Sukenick, Jamil Azzi, Gang Lin

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. The immunoproteasome regulates ILC2 responses by modulating mitochondrial capacity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Review
  4. 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.

Wenhu ZhanDepartment of Microbiology & Immunology, Weill Cornell Medicine, 1300 York Ave., New York, New York 10065, United States.ORCID 0000-0002-7095-7081
Daqiang LiDepartment of Microbiology & Immunology, Weill Cornell Medicine, 1300 York Ave., New York, New York 10065, United States.ORCID 0000-0001-8762-3339
Priya SahaDepartment of Microbiology & Immunology, Weill Cornell Medicine, 1300 York Ave., New York, New York 10065, United States.
Rong WangNMR Analytical Core Facility, Memorial Sloan Kettering Cancer Center, New York, New York 10065, United States.
Hao ZhangDepartment of Microbiology & Immunology, Weill Cornell Medicine, 1300 York Ave., New York, New York 10065, United States.ORCID 0000-0002-1187-5844
Amrendra K AjayRenal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, United States.ORCID 0000-0003-2790-5726
Christa DebanTransplantation Research Center, Renal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, United States.
George SukenickNMR Analytical Core Facility, Memorial Sloan Kettering Cancer Center, New York, New York 10065, United States.
Jamil AzziRenal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, United States.
Gang LinDepartment of Microbiology & Immunology, Weill Cornell Medicine, 1300 York Ave., New York, New York 10065, United States.ORCID 0000-0003-4797-7073

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Selective Plasmodium proteasome inhibitors as novel multi-stage antimalarialsR01AI143714 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI Gang Lin · 2019 to 2026
$6.1M
The novel role of the immunoproteasome subunit LMP7 in allo-immunity and T cell exhaustionR01AI134842 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI AZZI, JAMIL · 2018 to 2022
$1.9M
NCI NIH HHS P30 CA008748NIAID NIH HHS R01 AI134842NIAID NIH HHS R01 AI143714
6 · The paper itself

Abstract

We describe our discovery and development of potent and highly selective inhibitors of human constitutive proteasome chymotryptic activity (β5c). Structure-activity relationship studies of the novel class of inhibitors focused on optimization of

Indexed as

AsparagineProteasome Endopeptidase ComplexHumansKineticsProteasome InhibitorsStructure-Activity RelationshipAsparagineProteasome Endopeptidase ComplexProteasome Inhibitors

Identifiers

PMID36608337
PMCPMC10157300

What OpenQuestion holds

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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.