Evidence map›Paper›PMID 35384570›Full record

ArticleEJNMMI radiopharmacy and chemistry2022

Novel [

Mylène Richard, Françoise Hinnen, Bertrand Kuhnast

Abstract read
In one paragraph

Article in EJNMMI radiopharmacy and chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. The [18F] F-PSMA Probe: Chemical Perspectives.Current medicinal chemistry · 2025
    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

3 authors.

Mylène RichardUniversité Paris-Saclay, CEA, CNRS, Inserm, BioMaps, 91401, Orsay, France. mylene.richard@cea.fr.ORCID http://orcid.org/0000-0003-0305-578X
Françoise HinnenUniversité Paris-Saclay, CEA, CNRS, Inserm, BioMaps, 91401, Orsay, France.
Bertrand KuhnastUniversité Paris-Saclay, CEA, CNRS, Inserm, BioMaps, 91401, Orsay, France.

Funding

Agence Nationale de la Recherche ANR-17-CE18-0019
6 · The paper itself

Abstract

backgroundProsthetic approach for the radiolabeling of biologics with fluorine-18 is a robust strategy and has been employed for many years. It requires fast, biocompatible and selective reactions suited to these fragile molecules. Michael addition of a nucleophilic thiol moiety on α,β-unsaturated carbonyl entities is an interesting compromise between simplicity of preparation of the prosthetic reagent and control of the selectivity of the addition. The α,β-unsaturated carbonyl entity of the biologic can easily be generated by addition of a maleimide function using adequate heterobifunctional linkers or generated by selective modification of a cysteine residue leading to a dehydroalanine moiety. We report here the design, synthesis and radiosynthesis of a new fluoropyridine-based thiol [

resultsThe preparation of cold reference and labeling precursor of [

conclusionWe have developed an original [

Indexed as

DhaFluorine-18MaleimidePETProsthetic groupThiols

Identifiers

PMID35384570
PMCPMC8986957

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.