Evidence map›Paper›PMID 36320884›Full record

ArticleRSC chemical biology2022

The covalent reactivity of functionalized 5-hydroxy-butyrolactams is the basis for targeting of fatty acid binding protein 5 (FABP5) by the neurotrophic agent MT-21.

Esben B Svenningsen, Rasmus N Ottosen, Katrine H Jørgensen, Marija Nisavic, Camilla K Larsen, Bente K Hansen, Yong Wang, Kresten Lindorff-Larsen, Thomas Tørring, Stephan M Hacker and 2 more

Abstract read
In one paragraph

Article in RSC chemical biology, 2022. 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

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

12 authors.

Esben B SvenningsenDepartment of Chemistry, Aarhus University, DK-8000 Aarhus C Denmark thpou@chem.au.dk.ORCID https://orcid.org/0000-0001-5118-6499
Rasmus N OttosenDepartment of Chemistry, Aarhus University, DK-8000 Aarhus C Denmark thpou@chem.au.dk.
Katrine H JørgensenDepartment of Chemistry, Aarhus University, DK-8000 Aarhus C Denmark thpou@chem.au.dk.
Marija NisavicDepartment of Chemistry, Aarhus University, DK-8000 Aarhus C Denmark thpou@chem.au.dk.
Camilla K LarsenDepartment of Engineering - Microbial Biosynthesis, Aarhus University DK-8000 Aarhus C Denmark.
Bente K HansenDepartment of Chemistry, Aarhus University, DK-8000 Aarhus C Denmark thpou@chem.au.dk.
Yong WangCopenhagen Biocenter, University of Copenhagen DK-2200 Copenhagen N Denmark.ORCID https://orcid.org/0000-0001-9156-0377
Kresten Lindorff-LarsenCopenhagen Biocenter, University of Copenhagen DK-2200 Copenhagen N Denmark.ORCID https://orcid.org/0000-0002-4750-6039
Thomas TørringDepartment of Engineering - Microbial Biosynthesis, Aarhus University DK-8000 Aarhus C Denmark.
Stephan M HackerLeiden Institute of Chemistry, Leiden University NL-2333 CC Leiden The Netherlands.ORCID https://orcid.org/0000-0001-5420-4824
Johan PalmfeldtDepartment of Clinical Medicine - Research Unit for Molecular Medicine, Aarhus University Hospital DK-8200 Aarhus N Denmark.
Thomas B PoulsenDepartment of Chemistry, Aarhus University, DK-8000 Aarhus C Denmark thpou@chem.au.dk.ORCID https://orcid.org/0000-0002-0763-9996

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Covalently acting compounds experience a strong interest within chemical biology both as molecular probes in studies of fundamental biological mechanisms and/or as novel drug candidates. In this context, the identification of new classes of reactive groups is particularly important as these can expose novel reactivity modes and, consequently, expand the ligandable proteome. Here, we investigated the electrophilic reactivity of the 3-acyl-5-hydroxy-1,5-dihydro-2

Identifiers

PMID36320884
PMCPMC9533406

What OpenQuestion holds

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Registered trials

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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.