Evidence map›Paper›PMID 35479808›Full record

ArticleRSC advances2021

Anticancer activity of pyrimidodiazepines based on 2-chloro-4-anilinoquinazoline: synthesis, DNA binding and molecular docking.

Viviana Cuartas, Alberto Aragón-Muriel, Yamil Liscano, Dorian Polo-Cerón, Maria Del Pilar Crespo-Ortiz, Jairo Quiroga, Rodrigo Abonia, Braulio Insuasty

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  5. Article
  6. Pharmaceuticals (Basel, Switzerland) · 2022
    Article
  7. New Oxazolo[5,4-International journal of molecular sciences · 2022
    Article
  8. 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

8 authors at 3 institutions in 2 countries.

Viviana CuartasHeterocyclic Compounds Research Group, Department of Chemistry, Universidad del Valle A.A. 25360 Cali Colombia braulio.insuasty@correounivalle.edu.co +57-2339-3248 +57-315-484-6665.ORCID https://orcid.org/0000-0003-3776-9641
Alberto Aragón-MurielLaboratorio de Investigación en Catálisis y Procesos (LICAP), Departamento de Química, Universidad del Valle Cali 760001 Colombia.
Yamil LiscanoGrupo de Investigación en Química y Biotecnología (QUIBIO), Universidad Santiago de Cali Cali 760035 Colombia.
Dorian Polo-CerónLaboratorio de Investigación en Catálisis y Procesos (LICAP), Departamento de Química, Universidad del Valle Cali 760001 Colombia.
Maria Del Pilar Crespo-OrtizGrupo de Biotecnología e Infecciones Bacterianas, Departamento de Microbiología, Universidad del Valle Cali 760043 Colombia.
Jairo QuirogaHeterocyclic Compounds Research Group, Department of Chemistry, Universidad del Valle A.A. 25360 Cali Colombia braulio.insuasty@correounivalle.edu.co +57-2339-3248 +57-315-484-6665.
Rodrigo AboniaHeterocyclic Compounds Research Group, Department of Chemistry, Universidad del Valle A.A. 25360 Cali Colombia braulio.insuasty@correounivalle.edu.co +57-2339-3248 +57-315-484-6665.
Braulio InsuastyHeterocyclic Compounds Research Group, Department of Chemistry, Universidad del Valle A.A. 25360 Cali Colombia braulio.insuasty@correounivalle.edu.co +57-2339-3248 +57-315-484-6665.ORCID https://orcid.org/0000-0001-8371-3310
Hess (United States) · USUniversidad del Valle · COUniversidad Santiago de Cali · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multidrug resistance to chemotherapy is a critical health problem associated with mutation of the therapeutic target. Therefore, the development of anticancer agents remains a challenge to overcome cancer cell resistance. Herein, a new series of quinazoline-based pyrimidodiazepines 16a-g were synthesized by the cyclocondensation reaction of 2-chloro-4-anilinoquinazoline-chalcones 14a-g with 2,4,5,6-tetraaminopyrimidine. All quinazoline derivatives 14a-g and 16a-g were selected by the U.S. National Cancer Institute (NCI) for testing their anticancer activity against 60 cancer cell lines of different panels of human tumors. Among the tested compounds, quinazoline-chalcone 14g displayed high antiproliferative activity with GI

Identifiers

PMID35479808
PMCPMC9036565
OpenAlexW3177473261

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.