Evidence map›Paper›PMID 37974952›Full record

ArticleACS medicinal chemistry letters2023

Development and Utilization of Novel Transglutaminase 2 Inhibitors for Potential Treatment of Autoimmune Disease and Gastrointestinal Disorder.

Robert B Kargbo

Open access · greenAbstract readEditorial
In one paragraph

Article in ACS medicinal chemistry letters, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

1 author at 1 institution in 1 country.

Robert B KargboUsona Institute, Fitchburg, Wisconsin 53711-5300, United States.ORCID https://orcid.org/0000-0002-5539-6343
Usona Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transglutaminases, classified explicitly as "protein-glutamine: amine γ-glutamyl transferases", catalyze the formation of isopeptide bonds between the γ-amino group of lysine and the γ-glutamyl group of glutamine, leading to the release of ammonia. These enzymes play pivotal roles in diverse medical conditions such as cardiovascular, autoimmune, neurodegenerative, and dermatological diseases, as well as in wound healing and inflammatory diseases. This Patent Highlight presents novel inhibitors of transglutaminases, specifically transglutaminase 2 (TG2), and their synthetic processes. In addition, these inhibitors are effective treatments for diseases linked to TG2, such as celiac disease and fibrotic disorders. Therefore, these inhibitors can be active agents in pharmaceutical treatments.

Identifiers

PMID37974952
PMCPMC10641919
OpenAlexW4387770111

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.