Evidence map›Paper›PMID 39211216›Full record

ArticlebioRxiv : the preprint server for biology2024

Keita Nakane, Christophe Morisseau, Presley D Dowker-Key, Gabrielle Benitez, Jennifer T Aguilan, Emiko Nagai, Simone Sidoli, Bruce D Hammock, Ahmed Bettaieb, Kosaku Shinoda and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

  • Updated by
    2024
5 · Who and what money

Authors and funding

11 authors.

Keita Nakane
Christophe MorisseauORCID 0000-0002-5672-6631
Presley D Dowker-Key
Gabrielle Benitez
Jennifer T Aguilan
Bruce D Hammock
Kosaku Shinoda

Funding

Expanding the chemical probe development paradigm toward underexplored targetsR35GM155249 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Seiya Kitamura · 2024 to 2026
$1.3M
NIGMS NIH HHS R35 GM155249
6 · The paper itself

Abstract

Soluble epoxide hydrolase (sEH) is a bifunctional enzyme involved in fatty acid metabolism and promising drug target. We previously reported first-generation sEH proteolysis-targeting chimeras (PROTACs) with limited degradation potency and low aqueous and metabolic stability. Herein, we report the development of next-generation sEH PROTAC molecules with improved stability and degradation potency. One of the most potent molecules (compound

Identifiers

PMID39211216
PMCPMC11361158

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.