Evidence map›Paper›PMID 25961015›Full record

ArticleBioMed research international2015

Prediction of antifungal activity of gemini imidazolium compounds.

Łukasz Pałkowski, Jerzy Błaszczyński, Andrzej Skrzypczak, Jan Błaszczak, Alicja Nowaczyk, Joanna Wróblewska, Sylwia Kożuszko, Eugenia Gospodarek, Roman Słowiński, Jerzy Krysiński

Abstract read
In one paragraph

Article in BioMed research international, 2015. 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

10 authors.

Łukasz PałkowskiDepartment of Pharmaceutical Technology, Nicolaus Copernicus University, Jurasza 2, 85-094 Bydgoszcz, Poland.
Jerzy BłaszczyńskiInstitute of Computing Science, Poznań University of Technology, Piotrowo 2, 60-965 Poznań, Poland.
Andrzej SkrzypczakInstitute of Chemical Technology, Poznań University of Technology, Skłodowskiej-Curie 2, 60-965 Poznań, Poland.
Jan BłaszczakInstitute of Chemical Technology, Poznań University of Technology, Skłodowskiej-Curie 2, 60-965 Poznań, Poland.
Alicja NowaczykDepartment of Organic Chemistry, Nicolaus Copernicus University, Jurasza 2, 85-094 Bydgoszcz, Poland.
Joanna WróblewskaDepartment of Microbiology, Nicolaus Copernicus University, Skłodowskiej-Curie 9, 85-094 Bydgoszcz, Poland.
Sylwia KożuszkoDepartment of Microbiology, Nicolaus Copernicus University, Skłodowskiej-Curie 9, 85-094 Bydgoszcz, Poland.
Eugenia GospodarekDepartment of Microbiology, Nicolaus Copernicus University, Skłodowskiej-Curie 9, 85-094 Bydgoszcz, Poland.
Roman SłowińskiInstitute of Computing Science, Poznań University of Technology, Piotrowo 2, 60-965 Poznań, Poland ; Systems Research Institute, Polish Academy of Sciences, Newelska 6, 01-447 Warsaw, Poland.
Jerzy KrysińskiDepartment of Pharmaceutical Technology, Nicolaus Copernicus University, Jurasza 2, 85-094 Bydgoszcz, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The progress of antimicrobial therapy contributes to the development of strains of fungi resistant to antimicrobial drugs. Since cationic surfactants have been described as good antifungals, we present a SAR study of a novel homologous series of 140 bis-quaternary imidazolium chlorides and analyze them with respect to their biological activity against Candida albicans as one of the major opportunistic pathogens causing a wide spectrum of diseases in human beings. We characterize a set of features of these compounds, concerning their structure, molecular descriptors, and surface active properties. SAR study was conducted with the help of the Dominance-Based Rough Set Approach (DRSA), which involves identification of relevant features and relevant combinations of features being in strong relationship with a high antifungal activity of the compounds. The SAR study shows, moreover, that the antifungal activity is dependent on the type of substituents and their position at the chloride moiety, as well as on the surface active properties of the compounds. We also show that molecular descriptors MlogP, HOMO-LUMO gap, total structure connectivity index, and Wiener index may be useful in prediction of antifungal activity of new chemical compounds.

Indexed as

Antifungal AgentsCalcitriolCandida albicansCandidiasisDrug Resistance, FungalHumansImidazolesStructure-Activity Relationship1,25-dihydroxy-21-(3-hydroxy-3-methylbutyl)vitamin D(3)Antifungal AgentsCalcitriolimidazoleImidazoles

Identifiers

PMID25961015
PMCPMC4413040

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LicenceCC BY
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Registered trials

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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.