Evidence map›Paper›PMID 41113110›Full record

ArticleRSC medicinal chemistry2025

Design, synthesis and evaluation of fluorescent dihydropyridine-dihydropyrimidinone hybrids as inducers of cell-cycle arrest in a prostate cancer cell line

Vanessa P de Souza, Izabela N F Gomes, Samuel J Santos, Carolyne B Braga, Aryel J A Bezerra, Eric A Philot, Cíntia R N Ramos, Simone Q Pantaleão, Luciane S da Silva, Ronaldo A Pilli and 3 more

Abstract read
In one paragraph

Article in RSC medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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

13 authors.

Vanessa P de SouzaLaboratório de Sínteses Orgânicas, Instituto de Química, Universidade Federal do Rio Grande do Sul Av. Bento Gonçalves, 9500 CEP 91501-970 Porto Alegre RS Brazil dennis@iq.ufrgs.br.
Izabela N F GomesMolecular Oncology Research Center, Barretos Cancer Hospital Antenor Duarte Villela, 1331 14784-400 Barretos SP Brazil renatokjso@gmail.com.
Samuel J SantosLaboratório de Sínteses Orgânicas, Instituto de Química, Universidade Federal do Rio Grande do Sul Av. Bento Gonçalves, 9500 CEP 91501-970 Porto Alegre RS Brazil dennis@iq.ufrgs.br.
Carolyne B BragaInstituto de Química, Universidade Estadual de Campinas Cidade Universitária Zeferino Vaz, CEP 13083-970, Barão Geraldo Campinas SP Brazil.
Aryel J A BezerraMolecular Oncology Research Center, Barretos Cancer Hospital Antenor Duarte Villela, 1331 14784-400 Barretos SP Brazil renatokjso@gmail.com.
Eric A PhilotMolecular Oncology Research Center, Barretos Cancer Hospital Antenor Duarte Villela, 1331 14784-400 Barretos SP Brazil renatokjso@gmail.com.
Cíntia R N RamosMolecular Oncology Research Center, Barretos Cancer Hospital Antenor Duarte Villela, 1331 14784-400 Barretos SP Brazil renatokjso@gmail.com.
Simone Q PantaleãoCenter for Mathematics, Computing, and Cognition, Federal University of ABC Santo André SP Brazil.
Luciane S da SilvaMolecular Oncology Research Center, Barretos Cancer Hospital Antenor Duarte Villela, 1331 14784-400 Barretos SP Brazil renatokjso@gmail.com.
Ronaldo A PilliInstituto de Química, Universidade Estadual de Campinas Cidade Universitária Zeferino Vaz, CEP 13083-970, Barão Geraldo Campinas SP Brazil.ORCID https://orcid.org/0000-0002-5919-7763
Rui M ReisMolecular Oncology Research Center, Barretos Cancer Hospital Antenor Duarte Villela, 1331 14784-400 Barretos SP Brazil renatokjso@gmail.com.ORCID https://orcid.org/0000-0002-9639-7940
Renato J S OliveiraMolecular Oncology Research Center, Barretos Cancer Hospital Antenor Duarte Villela, 1331 14784-400 Barretos SP Brazil renatokjso@gmail.com.
Dennis RussowskyLaboratório de Sínteses Orgânicas, Instituto de Química, Universidade Federal do Rio Grande do Sul Av. Bento Gonçalves, 9500 CEP 91501-970 Porto Alegre RS Brazil dennis@iq.ufrgs.br.ORCID https://orcid.org/0000-0001-5968-9760

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescent dihydropyridine-dihydropyrimidinone (DHP-DHPM) hybrids were easily synthesized through the combination of Hantzsch and Biginelli multicomponent reactions followed by a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC, click chemistry) protocol. Nine hybrids showed promising antitumor activity for the PC3 prostate cancer cell line, notably compounds 9d and 9g. Both hybrids exhibited high selectivity for tumor cells, with significant selectivity indices (SI), particularly 9g (SI >68.8). Selectivity was qualitatively observed by the internalization of the fluorescent hybrids through high-resolution confocal laser scanning microscopy (CLSM).

Identifiers

PMID41113110
PMCPMC12530137

What OpenQuestion holds

Textmetadata
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.