Evidence map›Paper›PMID 35456549›Full record

ArticlePharmaceutics2022

Biological Evaluation of New Thienopyridinium and Thienopyrimidinium Derivatives as Human Choline Kinase Inhibitors.

Pilar María Luque-Navarro, Elena Mariotto, Marco Ballarotto, Gianluca Rubbini, Francisco José Aguilar-Troyano, Alberto Fasiolo, Archimede Torretta, Emilio Parisini, Antonio Macchiarulo, Alejandro Laso and 4 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 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
0.8field-weighted citation impact, top 35% 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

0 citing papers in PubMed, 7 citations in OpenAlex.

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

14 authors at 4 institutions in 3 countries.

Pilar María Luque-NavarroDepartment of Pharmaceutical and Organic Chemistry, Faculty of Pharmacy, Campus of Cartuja, 18071 Granada, Spain.
Elena MariottoLaboratory of Oncohematology, Department of Woman's and Child's Health, University of Padova, 35128 Padova, Italy.ORCID 0000-0002-3960-8561
Marco BallarottoDepartment of Pharmaceutical Sciences, University of Perugia, Via del Liceo 1, 06123 Perugia, Italy.ORCID 0000-0003-2361-4841
Gianluca RubbiniDepartment of Pharmaceutical and Organic Chemistry, Faculty of Pharmacy, Campus of Cartuja, 18071 Granada, Spain.
Francisco José Aguilar-TroyanoDepartment of Pharmaceutical and Organic Chemistry, Faculty of Pharmacy, Campus of Cartuja, 18071 Granada, Spain.ORCID 0000-0001-5274-7219
Alberto FasioloDepartment of Pharmaceutical and Organic Chemistry, Faculty of Pharmacy, Campus of Cartuja, 18071 Granada, Spain.
Archimede TorrettaCenter for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia, Via Pascoli 70/3, 20133 Milano, Italy.
Emilio ParisiniCenter for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia, Via Pascoli 70/3, 20133 Milano, Italy.ORCID 0000-0002-5529-0039
Antonio MacchiaruloDepartment of Pharmaceutical Sciences, University of Perugia, Via del Liceo 1, 06123 Perugia, Italy.ORCID 0000-0001-9535-4183
Alejandro LasoDepartment of Biochemistry and Molecular Biology I, Faculty of Sciences, 18071 Granada, Spain.ORCID 0000-0003-1320-5067
Carmen MarcoDepartment of Biochemistry and Molecular Biology I, Faculty of Sciences, 18071 Granada, Spain.
Giampietro ViolaLaboratory of Oncohematology, Department of Woman's and Child's Health, University of Padova, 35128 Padova, Italy.ORCID 0000-0001-9329-165X
María Paz Carrasco-JimenezDepartment of Biochemistry and Molecular Biology I, Faculty of Sciences, 18071 Granada, Spain.ORCID 0000-0003-1300-5196
Luisa Carlota López-CaraDepartment of Pharmaceutical and Organic Chemistry, Faculty of Pharmacy, Campus of Cartuja, 18071 Granada, Spain.ORCID 0000-0003-1142-6448
Universidad de Granada · ESItalian Institute of Technology · ITUniversity of Padua · ITUniversity of Perugia · IT

Funding

Convocatoria 2019 Proyectos de I + D + i - RTI Tipo B "Ministerio de Innovación y Ciencia" PID2019-109294RB-I00Convocatoria 2020 Proyectos I+D+i del Programa Operativo FEDER 2020" B-CTS-216-UGR20
6 · The paper itself

Abstract

Due to its role in lipid biosynthesis, choline kinase α1 (CKα1) is an interesting target for the development of new antitumor agents. In this work, we present a series of 41 compounds designed based on the well-known and successful strategy of introducing thienopyridine and pyrimidine as bioisosteres of other heterocycles in active antitumor compounds. Notwithstanding the fact that some of these compounds do not show significant enzymatic inhibition, others, in contrast, feature substantially improved enzymatic and antiproliferative inhibition values. This is also confirmed by docking analysis, whereby compounds with longer linkers and thienopyrimidine cationic head have been identified as the most compelling. Among the best compounds is

Indexed as

antitumoral drugcholine kinase inhibitioncholine uptake

Identifiers

PMID35456549
PMCPMC9032693
OpenAlexW4220966716

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.