Evidence map›Paper›PMID 41208641›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025

Mn

Zoltán Garda, Agnès Pallier, Tibor Nagy, Frédéric Szeremeta, Éva Tóth

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. 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

5 authors.

Zoltán GardaCentre de Biophysique Moléculaire, CNRS UPR 4301, Université d'Orléans, rue Charles Sadron, Orléans, 45071, France.ORCID https://orcid.org/0000-0002-3904-2959
Agnès PallierCentre de Biophysique Moléculaire, CNRS UPR 4301, Université d'Orléans, rue Charles Sadron, Orléans, 45071, France.
Tibor NagyDepartment of Applied Chemistry, University of Debrecen, Egyetem tér 1, Debrecen, 4010, Hungary.
Frédéric SzeremetaCentre de Biophysique Moléculaire, CNRS UPR 4301, Université d'Orléans, rue Charles Sadron, Orléans, 45071, France.
Éva TóthCentre de Biophysique Moléculaire, CNRS UPR 4301, Université d'Orléans, rue Charles Sadron, Orléans, 45071, France.ORCID https://orcid.org/0000-0002-3200-6752

Funding

H2020 Marie Skłodowska-Curie Actions 101065389Nemzeti Kutatási Fejlesztési és Innovációs Hivatal NKFIH PD-138064University of Debrecen Publication Fund
6 · The paper itself

Abstract

L2 is a bisamide derivative of cyclohexyl-diamine tetraacetate (CDTA) containing one trifluoromethyl-piperidine- and one dimethyl-amide. While the amide functions are stable at pH 7, at pH 4.35 hydrolysis occurs after 1 day, and it is faster for the amide involving the piperidine. pH potentiometry showed lower basicity for L2 than for CDTA, and similar stability for the two complexes (pMn  =  8.28 vs. 8.68 for MnL2 and MnCDTA, respectively). The replacement of carboxylates by amides results in two orders of magnitude higher kinetic inertness for MnL2 (t

Indexed as

19Fcontrast agentmanganeseMRIparamagnetic relaxation

Identifiers

PMID41208641
PMCPMC12734688

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.