Evidence map›Paper›PMID 38708212›Full record

ArticleACS omega2024

Synthesis, Photophysical Properties, Theoretical Studies, and Living Cancer Cell Imaging Applications of New 7-(Diethylamino)quinolone Chalcones.

Daniel Insuasty, Mario Mutis, Jorge Trilleras, Luis A Illicachi, Juan D Rodríguez, Andrea Ramos-Hernández, Homero G San-Juan-Vergara, Christian Cadena-Cruz, José R Mora, José L Paz and 5 more

Abstract read
In one paragraph

Article in ACS omega, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

Daniel InsuastyDepartamento de Química y Biología, División de Ciencias Básicas, Universidad del Norte, Km 5 vía Puerto Colombia, Puerto Colombia 081007, Colombia.ORCID https://orcid.org/0000-0001-9662-9505
Mario MutisGrupo de Investigación en Compuestos Heterocíclicos, Facultad de Ciencias Básicas, Universidad del Atlántico, Puerto Colombia 081007, Colombia.
Jorge TrillerasGrupo de Investigación en Compuestos Heterocíclicos, Facultad de Ciencias Básicas, Universidad del Atlántico, Puerto Colombia 081007, Colombia.
Luis A IllicachiGrupo de Investigación en Química y Biotecnología, Facultad de Ciencias Básicas, Universidad Santiago de Cali, Calle 5. No. 62-00, Cali 760032, Colombia.
Juan D RodríguezPrograma de medicina, Facultad de Ciencias de la Salud, Universidad Libre, Km 7 vía Puerto Colombia, Puerto Colombia 081007, Colombia.ORCID https://orcid.org/0000-0001-5247-867X
Andrea Ramos-HernándezGrupo Química Supramolecular Aplicada, Semillero Electroquímica Aplicada, Facultad de Ciencias Básicas, Universidad del Atlántico, Puerto Colombia 081007, Colombia.
Homero G San-Juan-VergaraDepartamento de Medicina, División Ciencias de la Salud, Universidad del Norte, Km 5 vía Puerto Colombia, Puerto Colombia 081007, Colombia.
Christian Cadena-CruzDepartamento de Medicina, División Ciencias de la Salud, Universidad del Norte, Km 5 vía Puerto Colombia, Puerto Colombia 081007, Colombia.
José R MoraInstituto de Simulación Computacional (ISC-USFQ), Departamento de Ingeniería Química, Universidad San Francisco de Quito, Diego de Robles y Vía Interoceánica, Quito 170901, Ecuador.ORCID https://orcid.org/0000-0001-6128-9504
José L PazDepartamento Académico de Química Inorgánica, Facultad de Química e Ingeniería Química, Universidad Nacional Mayor de San Marcos, Apartado, 15081 Lima, Perú.ORCID https://orcid.org/0000-0002-6177-7919
Maximiliano Méndez-LópezDepartamento de Química y Biología, División de Ciencias Básicas, Universidad del Norte, Km 5 vía Puerto Colombia, Puerto Colombia 081007, Colombia.ORCID https://orcid.org/0000-0002-8919-2066
Edwin G PérezOrganic Chemistry Department, Faculty of Chemistry and Pharmacy, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.
Margarita E AliagaPhysical Chemistry Department, Faculty of Chemistry and Pharmacy, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.
Jhesua ValenciaDepartamento de Química y Biología, División de Ciencias Básicas, Universidad del Norte, Km 5 vía Puerto Colombia, Puerto Colombia 081007, Colombia.
Edgar MárquezDepartamento de Química y Biología, División de Ciencias Básicas, Universidad del Norte, Km 5 vía Puerto Colombia, Puerto Colombia 081007, Colombia.ORCID https://orcid.org/0000-0002-7503-1528

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this article, three unsymmetrical 7-(diethylamino)quinolone chalcones with D-π-A-D and D-π-A-π-D type push-pull molecular arrangements were synthesized via a Claisen-Schmidt reaction. Using 7-(diethylamino)quinolone and vanillin as electron donor (D) moieties, these were linked together through the α,β-unsaturated carbonyl system acting as a linker and an electron acceptor (A). The photophysical properties were studied, revealing significant Stokes shifts and strong solvatofluorochromism caused by the ICT and TICT behavior produced by the push-pull effect. Moreover, quenching caused by the population of the TICT state in THF-H

Identifiers

PMID38708212
PMCPMC11064003

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.