Evidence map›Paper›PMID 39296790›Full record

ArticleTurkish journal of chemistry2024

Synthesis and characterization of new hexahydroquinoline derivatives and evaluation of their cytotoxicity, intracellular ROS production, and inhibitory effects on inflammatory mediators.

Ezgi Pehlivanlar, Deniz Arca Çakir, Sonia Sanajou, Hülya Tezel Yalçin, Terken Baydar, Pınar Erkekoğlu, Hanife Avci, Rahime Şimşek

Abstract read
In one paragraph

Article in Turkish journal of chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Ezgi PehlivanlarDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-4088-7721
Deniz Arca ÇakirDepartment of Toxicology, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-6110-1775
Sonia SanajouDepartment of Toxicology, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-6751-5266
Hülya Tezel YalçinDepartment of Toxicology, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-1843-3424
Terken BaydarDepartment of Toxicology, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-5497-9600
Pınar ErkekoğluDepartment of Toxicology, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0003-4713-7672
Hanife AvciDepartment of Biostatistics, School of Medicine, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-1405-9754
Rahime ŞimşekDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-8467-6336

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation is a response to injury and infection in an organism. It can be categorized as acute or chronic. Chronic inflammation is the underlying cause of many diseases such as Alzheimer disease, diabetes, rheumatoid arthritis, atherosclerosis, and cardiovascular diseases. Recent studies have proven the antiinflammatory properties of 1,4-dihydropyridines (1,4-DHPs) and their derivatives, which have many biological activities including the blocking of calcium channels. In this study, 15 compounds that are condensed derivatives of 1,4-DHPs, with the general structure of hexahydroquinoline-3-carboxylate, were synthesized. These compounds, expected to show inhibitory activity against inflammatory mediators, were obtained by the reaction of 4-(difluoromethoxy)benzaldehyde, substituted/nonsubstituted 1,3-cyclohexanedione derivatives, and appropriate alkyl acetoacetate compounds in the presence of ammonium acetate as a nitrogen source according to the Hantzsch synthesis method. The structures of the synthesized compounds were elucidated by IR,

Indexed as

14-Dihydropyridinescytotoxicityhexahydroquinolineinflammationmolecular docking

Identifiers

PMID39296790
PMCPMC11407359

What OpenQuestion holds

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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.