Evidence map›Paper›PMID 35752294›Full record

ArticleChemico-biological interactions2022

A new class of half-sandwich ruthenium complexes containing Biginelli hybrids: anticancer and anti-SARS-CoV-2 activities.

Nenad Janković, Emilija Milović, Jelena Đorović Jovanović, Zoran Marković, Milan Vraneš, Tatjana Stanojković, Ivana Matić, Marija Đorđić Crnogorac, Olivera Klisurić, Miroslav Cvetinov and 1 more

Abstract read
In one paragraph

Article in Chemico-biological interactions, 2022. 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. Review
  2. Article
  3. Review
  4. Metallo-antiviral aspirants:European journal of medicinal chemistry reports · 2023
    Review
  5. Article
  6. Review
  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

11 authors.

Nenad JankovićUniversity of Kragujevac, Institute for Information Technologies Kragujevac, Department of Science, Jovana Cvijića bb, Kragujevac, 34000, Serbia. Electronic address: nenad.jankovic@kg.ac.rs.
Emilija MilovićUniversity of Kragujevac, Institute for Information Technologies Kragujevac, Department of Science, Jovana Cvijića bb, Kragujevac, 34000, Serbia.
Jelena Đorović JovanovićUniversity of Kragujevac, Institute for Information Technologies Kragujevac, Department of Science, Jovana Cvijića bb, Kragujevac, 34000, Serbia.
Zoran MarkovićUniversity of Kragujevac, Institute for Information Technologies Kragujevac, Department of Science, Jovana Cvijića bb, Kragujevac, 34000, Serbia.
Milan VranešFaculty of Science, Department of Chemistry, Biochemistry and Environmental Protection, University of Novi Sad, Trg Dositeja Obradovića 3, 21000, Novi Sad, Serbia.
Tatjana StanojkovićInstitute for Oncology and Radiology of Serbia, Pasterova 14, 11000, Belgrade, Serbia.
Ivana MatićInstitute for Oncology and Radiology of Serbia, Pasterova 14, 11000, Belgrade, Serbia.
Marija Đorđić CrnogoracInstitute for Oncology and Radiology of Serbia, Pasterova 14, 11000, Belgrade, Serbia.
Olivera KlisurićUniversity of Novi Sad, Faculty of Science, Department of Physics, Trg Dositeja Obradovića 3, 21000, Novi Sad, Serbia.
Miroslav CvetinovAcademy of Arts, University of Novi Sad, Đure Jakšića 7, Novi Sad, Serbia.
Syed Nasir Abbas BukhariDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Aljouf, Sakaka, 72388, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to discover new dual-active agents, a series of novel Biginelli hybrids (tetrahydropyrimidines) and their ruthenium(II) complexes were synthesized. Newly synthesized compounds were characterized by IR, NMR, and X-ray techniques and investigated for their cytotoxic effect on human cancer cell lines HeLa, LS174, A549, A375, K562 and normal fibroblasts (MRC-5). For further examination of the cytotoxic mechanisms of novel complexes, two of them were chosen for analyzing their effects on the distribution of HeLa cells in the cell cycle phases. The results of the flow cytometry analysis suggest that the proportion of cells in G2/M phase was decreased following the increase of subG1 phase in all treatments. These results confirmed that cells treated with 5b and 5c were induced to undergo apoptotic death. The ruthenium complexes 5a-5d show significant inhibitory potency against SARS-CoV-2 M

Indexed as

Antineoplastic AgentsCoordination ComplexesCOVID-19 Drug TreatmentRutheniumCell Line, TumorDose-Response Relationship, DrugDrug Screening Assays, AntitumorHeLa CellsHumansSARS-CoV-2Antineoplastic AgentsCoordination ComplexesRutheniumAnticancerCOVID-19RutheniumSARS-CoV-2 M(pro)Tetrahydropyrimidines

Identifiers

PMID35752294
PMCPMC9220501

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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.