Evidence map›Paper›PMID 37569665›Full record

ArticleInternational journal of molecular sciences2023

Unravelling the Role of Uncommon Hydrogen Bonds in Cyclodextrin Ferrociphenol Supramolecular Complexes: A Computational Modelling and Experimental Study.

Pascal Pigeon, Feten Najlaoui, Michael James McGlinchey, Juan Sanz García, Gérard Jaouen, Stéphane Gibaud

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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 4 institutions in 2 countries.

Pascal PigeonChimie ParisTech, PSL, 11 Rue Pierre et Marie Curie, CEDEX 05, 75231 Paris, France.ORCID 0000-0001-5374-5346
Feten NajlaouiEA 3452/CITHEFOR, Faculté de Pharmacie, Université de Lorraine, 5 Rue Albert Lebrun, 54000 Nancy, France.
Michael James McGlincheyUCD School of Chemistry, University College Dublin Belfield, D04 V1W8 Dublin, Ireland.
Juan Sanz García1MSME, Université Gustave Eiffel, CNRS, 5 Boulevard Descartes, 77454 Marne-la-Vallée, France.ORCID 0000-0002-3175-0061
Gérard JaouenChimie ParisTech, PSL, 11 Rue Pierre et Marie Curie, CEDEX 05, 75231 Paris, France.
Stéphane GibaudEA 3452/CITHEFOR, Faculté de Pharmacie, Université de Lorraine, 5 Rue Albert Lebrun, 54000 Nancy, France.ORCID 0000-0003-3594-0601
Chimie ParisTech · FRCibles thérapeutiques, formulation et expertise préclinique du médicamentCentre National de la Recherche Scientifique · FRUniversity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We sought to determine the cyclodextrins (CDs) best suited to solubilize a patented succinimido-ferrocidiphenol (SuccFerr), a compound from the ferrociphenol family having powerful anticancer activity but low water solubility. Phase solubility experiments and computational modelling were carried out on various CDs. For the latter, several CD-SuccFerr complexes were built starting from combinations of one or two CD(s) where the methylation of CD oxygen atoms was systematically changed to end up with a database of ca. 13 k models. Modelling and phase solubility experiments seem to indicate the predominance of supramolecular assemblies of SuccFerr with two CDs and the superiority of randomly methylated β-cyclodextrins (RAMEβCDs). In addition, modelling shows that there are several competing combinations of inserted moieties of SuccFerr. Furthermore, the models show that ferrocene can contribute to high stabilization by making atypical hydrogen bonds between Fe and the hydroxyl groups of CDs (single bond with one OH or clamp with two OH of the same glucose unit).

Indexed as

beta-CyclodextrinsCyclodextrinsComputer SimulationFerrous CompoundsHydrogen BondingSolubilitybeta-CyclodextrinsCyclodextrinsferrociphenolFerrous Compoundsatypical hydrogen bondcyclodextrindatabaseferrocenemodellingphase solubility

Identifiers

PMID37569665
PMCPMC10419020
OpenAlexW4385456037

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.