Evidence map›Paper›PMID 38283221›Full record

ArticleRSC medicinal chemistry2024

Discovery of imidazo[1,2-

Desmond Akwata, Allison L Kempen, Jones Lamptey, Neetu Dayal, Nickolas R Brauer, Herman O Sintim

Open access · hybridAbstract read
In one paragraph

Article in RSC medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.9field-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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

6 authors at 1 institution in 1 country.

Desmond AkwataDepartment of Chemistry, Purdue University 560 Oval Drive West Lafayette IN 47907 USA hsintim@purdue.edu.
Allison L KempenDepartment of Chemistry, Purdue University 560 Oval Drive West Lafayette IN 47907 USA hsintim@purdue.edu.ORCID https://orcid.org/0009-0003-6856-5147
Jones LampteyDepartment of Chemistry, Purdue University 560 Oval Drive West Lafayette IN 47907 USA hsintim@purdue.edu.
Neetu DayalDepartment of Chemistry, Purdue University 560 Oval Drive West Lafayette IN 47907 USA hsintim@purdue.edu.
Nickolas R BrauerDepartment of Chemistry, Purdue University 560 Oval Drive West Lafayette IN 47907 USA hsintim@purdue.edu.ORCID https://orcid.org/0009-0009-5349-2321
Herman O SintimDepartment of Chemistry, Purdue University 560 Oval Drive West Lafayette IN 47907 USA hsintim@purdue.edu.ORCID https://orcid.org/0000-0002-2280-9359
Purdue University West Lafayette · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current treatment options for patients with multiple myeloma (MM) include proteasome inhibitors, anti-CD38 antibodies, and immunomodulatory agents. However, if patients have continued disease progression after administration of these treatments, there are limited options. There is a need for effective targeted therapies of MM. Recent studies have shown that the transforming growth factor-β activated kinase (TAK1) is upregulated and overexpressed in MM. We have discovered that 6-substituted morpholine or piperazine imidazo[1,2-

Identifiers

PMID38283221
PMCPMC10809330
OpenAlexW4389104274

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.