Evidence map›Paper›PMID 32093112›Full record

ArticleMolecules (Basel, Switzerland)2020

Insight into GEBR-32a: Chiral Resolution, Absolute Configuration and Enantiopreference in PDE4D Inhibition.

Valeria Cavalloro, Katia Russo, Francesca Vasile, Luca Pignataro, Archimede Torretta, Stefano Donini, Marta S Semrau, Paola Storici, Daniela Rossi, Federica Rapetti and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

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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

14 authors at 5 institutions in 2 countries.

Valeria CavalloroDepartment of Drug Sciences, University of Pavia, 27100 Pavia, Italy.
Katia RussoDepartment of Drug Sciences, University of Pavia, 27100 Pavia, Italy.
Francesca VasileUniversità degli Studi di Milano, Dipartimento di Chimica, via C. Golgi 19, 20133 Milano, Italy.
Luca PignataroUniversità degli Studi di Milano, Dipartimento di Chimica, via C. Golgi 19, 20133 Milano, Italy.
Archimede TorrettaCenter for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia, Via Pascoli 70/3, 20133 Milano, Italy.
Stefano DoniniCenter for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia, Via Pascoli 70/3, 20133 Milano, Italy.
Marta S SemrauElettra-Sincrotrone Trieste S.C.p.A., SS 14-km 163.5 in AREA Science Park, 34149 Trieste, Italy.
Paola StoriciElettra-Sincrotrone Trieste S.C.p.A., SS 14-km 163.5 in AREA Science Park, 34149 Trieste, Italy.
Daniela RossiDepartment of Drug Sciences, University of Pavia, 27100 Pavia, Italy.
Federica RapettiDepartment of Pharmacy, Section of Medicinal Chemistry, School of Medical and Pharmaceutical Sciences, University of Genoa, 16132 Genoa, Italy.
Chiara BrulloDepartment of Pharmacy, Section of Medicinal Chemistry, School of Medical and Pharmaceutical Sciences, University of Genoa, 16132 Genoa, Italy.
Emilio ParisiniCenter for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia, Via Pascoli 70/3, 20133 Milano, Italy.
Olga BrunoDepartment of Pharmacy, Section of Medicinal Chemistry, School of Medical and Pharmaceutical Sciences, University of Genoa, 16132 Genoa, Italy.
Simona CollinaDepartment of Drug Sciences, University of Pavia, 27100 Pavia, Italy.
University of Pavia · ITItalian Institute of Technology · ITUniversity of Genoa · ITElettra-Sincrotrone Trieste S.C.p.A. · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease is the most common type of dementia, affecting millions of people worldwide. One of its main consequences is memory loss, which is related to downstream effectors of cyclic adenosine monophosphate (cAMP). A well-established strategy to avoid cAMP degradation is the inhibition of phosphodiesterase (PDE). In recent years, GEBR-32a has been shown to possess selective inhibitory properties against PDE type 4 family members, resulting in an improvement in spatial memory processes without the typical side effects that are usually correlated with this mechanism of action. In this work, we performed the HPLC chiral resolution and absolute configuration assignment of GEBR-32a. We developed an efficient analytical and semipreparative chromatographic method exploiting an amylose-based stationary phase, we studied the chiroptical properties of both enantiomers and we assigned their absolute configuration by

Indexed as

Cyclic Nucleotide Phosphodiesterases, Type 4HumansNuclear Magnetic Resonance, BiomolecularPhosphodiesterase 4 InhibitorsCyclic Nucleotide Phosphodiesterases, Type 4PDE4D protein, humanPhosphodiesterase 4 InhibitorsHPLC chiral resolutionNMR absolute configuration assignmentPDE4 inhibition

Identifiers

PMID32093112
PMCPMC7070305
OpenAlexW3008245751

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.