Evidence map›Paper›PMID 38998972›Full record

ArticleMolecules (Basel, Switzerland)2024

Synthesis and Biological Evaluation of New Compounds with Nitroimidazole Moiety.

Katarzyna Dziduch, Sara Janowska, Sylwia Andrzejczuk, Paulina Strzyga-Łach, Marta Struga, Marcin Feldo, Oleg Demchuk, Monika Wujec

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. 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

8 authors.

Katarzyna DziduchDoctoral School, Medical University of Lublin, Chodzki 7, 20-093 Lublin, Poland.ORCID 0000-0002-7543-1134
Sara JanowskaDepartment of Pathobiochemistry and Interdisciplinary Applications of Ion Chromatography, Biomedical Sciences, Medical University of Lublin, 1 Chodzki Street, 20-093 Lublin, Poland.ORCID 0000-0002-2881-7552
Sylwia AndrzejczukDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, Medical University, 20-093 Lublin, Poland.ORCID 0000-0001-6301-6059
Paulina Strzyga-ŁachChair and Department of Biochemistry, Medical University of Warsaw, 02-097 Warszawa, Poland.ORCID 0000-0003-1830-2210
Marta StrugaChair and Department of Biochemistry, Medical University of Warsaw, 02-097 Warszawa, Poland.ORCID 0000-0002-0181-3607
Marcin FeldoDepartment of Vascular Surgery, Medical University of Lublin, Staszica 11 St., 20-081 Lublin, Poland.
Oleg DemchukFaculty of Medicine, The John Paul II Catholic University of Lublin, Konstantynow 1J, 20-708 Lublin, Poland.ORCID 0000-0002-5571-1593
Monika WujecDepartment of Organic Chemistry, Faculty of Pharmacy, Medical University of Lublin, 4A Chodzki Street, 20-093 Lublin, Poland.ORCID 0000-0001-9816-1934

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterocyclic compounds, particularly those containing azole rings, have shown extensive biological activity, including anticancer, antibacterial, and antifungal properties. Among these, the imidazole ring stands out due to its diverse therapeutic potential. In the presented study, we designed and synthesized a series of imidazole derivatives to identify compounds with high biological potential. We focused on two groups: thiosemicarbazide derivatives and hydrazone derivatives. We synthesized these compounds using conventional methods and confirmed their structures via nuclear magnetic resonance spectroscopy (NMR), MS, and elemental analysis, and then assessed their antibacterial and antifungal activities in vitro using the broth microdilution method against Gram-positive and Gram-negative bacteria, as well as

Indexed as

Anti-Bacterial AgentsAntifungal AgentsAntineoplastic AgentsGram-Positive BacteriaMicrobial Sensitivity TestsCandidaCell Line, TumorGram-Negative BacteriaHumansHydrazonesMolecular StructureNitroimidazolesSemicarbazidesStructure-Activity RelationshipAnti-Bacterial AgentsAntifungal AgentsAntineoplastic AgentsHydrazonesNitroimidazolesSemicarbazidesthiosemicarbazideantibacterial activityanticancer activityhydrazide-hydrazonestructure-activity relationshipsynthesisthiosemicarbazide

Identifiers

PMID38998972
PMCPMC11243693

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.