Evidence map›Paper›PMID 34451880›Full record

ArticlePharmaceuticals (Basel, Switzerland)2021

Hybrid Quinolinyl Phosphonates as Heterocyclic Carboxylate Isosteres: Synthesis and Biological Evaluation against Topoisomerase 1B (TOP1B).

Asier Selas, María Fuertes, Estela Melcón-Fernández, Yolanda Pérez-Pertejo, Rosa M Reguera, Rafael Balaña-Fouce, Birgitta R Knudsen, Francisco Palacios, Concepcion Alonso

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Green-Light Photocatalysis: Borylated Benzo[The Journal of organic chemistry · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
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

9 authors.

Asier SelasDepartamento de Química Orgánica I, Facultad de Farmacia and Centro de Investigación Lascaray, Universidad del País Vasco (UPV/EHU), Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.ORCID 0000-0001-7327-668X
María FuertesDepartamento de Química Orgánica I, Facultad de Farmacia and Centro de Investigación Lascaray, Universidad del País Vasco (UPV/EHU), Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.
Estela Melcón-FernándezDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.
Yolanda Pérez-PertejoDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.
Rosa M RegueraDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0000-0001-9148-2997
Rafael Balaña-FouceDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0000-0003-0418-6116
Birgitta R KnudsenDepartment of Molecular Biology, Genetics and Interdisciplinary Nanoscience Center (iNANO), Aarhus University, 8000 Aarhus, Denmark.
Francisco PalaciosDepartamento de Química Orgánica I, Facultad de Farmacia and Centro de Investigación Lascaray, Universidad del País Vasco (UPV/EHU), Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.ORCID 0000-0001-6365-0324
Concepcion AlonsoDepartamento de Química Orgánica I, Facultad de Farmacia and Centro de Investigación Lascaray, Universidad del País Vasco (UPV/EHU), Paseo de la Universidad 7, 01006 Vitoria-Gasteiz, Spain.ORCID 0000-0003-0866-3493

Funding

Eusko Jaurlaritza IT 992-16Ministerio de Ciencia, Innovación y Universidades RTI2018-101818-B-I00Ministerio de Economía y Competitividad SAF2017-83575-R
6 · The paper itself

Abstract

This work describes, for the first time, the synthesis of dialkyl (2-arylquinolin-8-yl)phosphonate derivatives. The preparation was carried out through a direct and simple process as a multicomponent Povarov reaction of aminophenylphosphonates, aldehydes, and styrenes and subsequent oxidation with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) or, alternatively, by a cycloaddition reaction between phosphonate aldimines and acetylenes. Based on phosphonate group structural characteristics, considered as phosphorous isosteres of carboxylic heterocycles, they may present interesting biological properties related to cell proliferation. In the current report, a new series of dialkyl (2-arylquinolin-8-yl)phosphonates have been synthesized and their antiproliferative effect evaluated on different human cancer and embryonic cells, as well as on

Indexed as

antiproliferative effectenzyme inhibitionleishmaniosis effectquinolinyl phosphonatestopoisomerase 1B

Identifiers

PMID34451880
PMCPMC8399847

What Socratic 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 Socratic graph.