Evidence map›Paper›PMID 26114446›Full record

ArticlePloS one2015

Synthesis of New Styrylquinoline Cellular Dyes, Fluorescent Properties, Cellular Localization and Cytotoxic Behavior.

Marzena Rams-Baron, Mateusz Dulski, Anna Mrozek-Wilczkiewicz, Mateusz Korzec, Wioleta Cieslik, Ewelina Spaczyńska, Piotr Bartczak, Alicja Ratuszna, Jaroslaw Polanski, Robert Musiol

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Antifungal Styryloquinolines asMolecules (Basel, Switzerland) · 2020
    Article
  6. Article
  7. 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

10 authors.

Marzena Rams-BaronA. Chelkowski Institute of Physics, University of Silesia, Uniwersytecka 4, Katowice, 40-007, Poland; Silesian Center for Education and Interdisciplinary Research, 75 Pulku Piechoty 1A, Chorzow, 41-500, Poland.
Mateusz DulskiSilesian Center for Education and Interdisciplinary Research, 75 Pulku Piechoty 1A, Chorzow, 41-500, Poland; Institute of Material Sciences, University of Silesia, 75 Pulku Piechoty 1A, Chorzow, 41-500, Poland.
Anna Mrozek-WilczkiewiczA. Chelkowski Institute of Physics, University of Silesia, Uniwersytecka 4, Katowice, 40-007, Poland; Silesian Center for Education and Interdisciplinary Research, 75 Pulku Piechoty 1A, Chorzow, 41-500, Poland.
Mateusz KorzecInstitute of Chemistry, University of Silesia, Szkolna 9, Katowice, 40-006, Poland.
Wioleta CieslikInstitute of Chemistry, University of Silesia, Szkolna 9, Katowice, 40-006, Poland.
Ewelina SpaczyńskaInstitute of Chemistry, University of Silesia, Szkolna 9, Katowice, 40-006, Poland.
Piotr BartczakInstitute of Chemistry, University of Silesia, Szkolna 9, Katowice, 40-006, Poland.
Alicja RatusznaA. Chelkowski Institute of Physics, University of Silesia, Uniwersytecka 4, Katowice, 40-007, Poland; Silesian Center for Education and Interdisciplinary Research, 75 Pulku Piechoty 1A, Chorzow, 41-500, Poland.
Jaroslaw PolanskiInstitute of Chemistry, University of Silesia, Szkolna 9, Katowice, 40-006, Poland.
Robert MusiolInstitute of Chemistry, University of Silesia, Szkolna 9, Katowice, 40-006, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New styrylquinoline derivatives with their photophysical constants are described. The synthesis was achieved via Sonogashira coupling using the newly developed heterogeneous nano-Pd/Cu catalyst system, which provides an efficient synthesis of high purity products. The compounds were tested in preliminary fluorescent microscopy studies to in order to identify their preferable cellular localization, which appeared to be in the lipid cellular organelles. The spectroscopic properties of the compounds were measured and theoretical TD-DFT calculations were performed. A biological analysis of the quinolines that were tested consisted of cytotoxicity assays against normal human fibroblasts and colon adenocarcinoma cells. All of the compounds that were studied appeared to be safe and indifferent to cells in a high concentration range. The presented results suggest that the quinoline compounds that were investigated in this study may be valuable structures for development as fluorescent dyes that could have biological applications.

Indexed as

CytotoxinsFluorescent DyesQuinolinesCell Line, TumorHumansCytotoxinsFluorescent DyesQuinolinesstyrylquinoline

Identifiers

PMID26114446
PMCPMC4482625

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.