Evidence map›Paper›PMID 21072023›Full record

ArticleMolecules (Basel, Switzerland)2010

Investigating the spectrum of biological activity of ring-substituted salicylanilides and carbamoylphenylcarbamates.

Jan Otevrel, Zuzana Mandelova, Matus Pesko, Jiahui Guo, Katarina Kralova, Frantisek Sersen, Marcela Vejsova, Danuta S Kalinowski, Zaklina Kovacevic, Aidan Coffey and 3 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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  11. Synthesis and Spectrum of Biological Activities of Novel N-arylcinnamamides.International journal of molecular sciences · 2018
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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.

Jan OtevrelDepartment of Chemical Drugs, University of Veterinary and Pharmaceutical Sciences, Brno, Czech Republic.
Zuzana Mandelova
Matus Pesko
Jiahui Guo
Katarina Kralova
Frantisek Sersen
Marcela Vejsova
Danuta S Kalinowski
Zaklina Kovacevic
Aidan Coffey
Jozef Csollei
Des R Richardson
Josef Jampilek

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, a series of twelve ring-substituted salicylanilides and carbamoylphenylcarbamates were prepared and characterized. The compounds were analyzed using RP-HPLC to determine lipophilicity. They were tested for their activity related to the inhibition of photosynthetic electron transport (PET) in spinach (Spinacia oleracea L.) chloroplasts. Moreover, their site of action in the photosynthetic apparatus was determined. Primary in vitro screening of the synthesized compounds was also performed against mycobacterial, bacterial and fungal strains. Several compounds showed biological activity comparable with or higher than the standards 3-(3,4-dichlorophenyl)-1,1-dimethylurea, isoniazid, penicillin G, ciprofloxacin or fluconazole. The most active compounds showed minimal anti-proliferative activity against human cells in culture, indicating they would have low cytotoxicity. For all compounds, the relationships between lipophilicity and the chemical structure are discussed.

Indexed as

AbsidiaAnti-Bacterial AgentsAntifungal AgentsCell Line, TumorCell ProliferationChloroplastsElectron TransportHerbicidesHumansMicrobial Sensitivity TestsPhenylcarbamatesPhotosynthesisSalicylanilidesSpinacia oleraceaStaphylococcus aureusStaphylococcus epidermidisAnti-Bacterial AgentsAntifungal AgentsHerbicidesPhenylcarbamatesSalicylanilides

Identifiers

PMID21072023
PMCPMC6259458

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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.