Evidence map›Paper›PMID 34236855›Full record

ArticleJournal of medicinal chemistry2021

Carbohydrate-Based NK1R Antagonists with Broad-Spectrum Anticancer Activity.

Rocío Recio, Patricia Lerena, Esther Pozo, José Manuel Calderón-Montaño, Estefanía Burgos-Morón, Miguel López-Lázaro, Victoria Valdivia, Manuel Pernia Leal, Bernard Mouillac, Juan Ángel Organero and 2 more

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
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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

12 authors.

Rocío RecioDepartamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.
Patricia LerenaDepartamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.ORCID 0000-0002-5048-9524
Esther PozoDepartamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.
José Manuel Calderón-MontañoDepartamento de Farmacología, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.
Estefanía Burgos-MorónDepartamento de Farmacología, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.
Miguel López-LázaroDepartamento de Farmacología, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.
Victoria ValdiviaDepartamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.
Manuel Pernia LealDepartamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.ORCID 0000-0001-8160-0574
Bernard MouillacInstitut de Génomique Fonctionnelle (IGF), INSERM, Université de Montpellier, CNRS, F-34094 Montpellier, France.
Juan Ángel OrganeroDepartamento de Química Física, Facultad de Ciencias Ambientales y Bioquímicas and INAMOL, Universidad de Castilla-La Mancha, Avenida Carlos III, s/n, 45071 Toledo, Spain.
Noureddine KhiarInstituto de Investigaciones Químicas (IIQ), CSIC-Universidad de Sevilla, Avenida Américo Vespucio, 49, Isla de la Cartuja, 41092 Sevilla, Spain.ORCID 0000-0003-4211-7138
Inmaculada FernándezDepartamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad de Sevilla, C/ Profesor García González, 2, 41012 Sevilla, Spain.ORCID 0000-0002-3468-387X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NK1R antagonists, investigated for the treatment of several pathologies, have shown encouraging results in the treatment of several cancers. In the present study, we report on the synthesis of carbohydrate-based NK1R antagonists and their evaluation as anticancer agents against a wide range of cancer cells. All of the prepared compounds, derived from either d-galactose or l-arabinose, have shown high affinity and NK1R antagonistic activity with a broad-spectrum anticancer activity and an important selectivity, comparable to Cisplatin. This strategy has allowed us to identify the galactosyl derivative

Indexed as

AnimalsAntineoplastic AgentsCarbohydratesCell ProliferationCells, CulturedCricetulusDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansMolecular StructureReceptors, Neurokinin-1Structure-Activity RelationshipAntineoplastic AgentsCarbohydratesReceptors, Neurokinin-1TACR1 protein, human

Identifiers

PMID34236855
PMCPMC8529873

What OpenQuestion holds

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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.