Evidence map›Paper›PMID 32168943›Full record

ArticleInternational journal of molecular sciences2020

New Arylethanolimidazole Derivatives as HO-1 Inhibitors with Cytotoxicity against MCF-7 Breast Cancer Cells.

Valeria Ciaffaglione, Sebastiano Intagliata, Valeria Pittalà, Agostino Marrazzo, Valeria Sorrenti, Luca Vanella, Antonio Rescifina, Giuseppe Floresta, Ameera Sultan, Khaled Greish and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
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  5. Review
  6. Heme Oxygenase Modulation Drives Ferroptosis in TNBC Cells.International journal of molecular sciences · 2022
    Article
  7. Article
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  10. Article
  11. Article
  12. Review
  13. Article
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  15. Review
  16. Novel Heme Oxygenase-1 (HO-1) Inducers Based on Dimethyl Fumarate Structure.International journal of molecular sciences · 2020
    Article
  17. Article
  18. 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

11 authors.

Valeria CiaffaglioneDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.
Sebastiano IntagliataDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0002-0201-1745
Valeria PittalàDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0003-1856-0308
Agostino MarrazzoDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0002-8728-8857
Valeria SorrentiDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0002-5973-1495
Luca VanellaDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0002-6314-6029
Antonio RescifinaDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0001-5039-2151
Giuseppe FlorestaDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0002-0668-1260
Ameera SultanDepartment of Molecular Medicine, College of Medicine and Medical Sciences, Princess Al-Jawhara Centre for Molecular Medicine, Arabian Gulf University, Manama 329, Bahrain.
Khaled GreishDepartment of Molecular Medicine, College of Medicine and Medical Sciences, Princess Al-Jawhara Centre for Molecular Medicine, Arabian Gulf University, Manama 329, Bahrain.ORCID 0000-0002-0787-7070
Loredana SalernoDepartment of Drug Sciences, University of Catania, viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0001-6458-3717

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this paper, a novel series of imidazole-based heme oxygenase-1 (HO-1) inhibitors is reported. These compounds were obtained by modifications of previously described high potent and selective arylethanolimidazoles. In particular, simplification of the central linker and repositioning of the hydrophobic portion were carried out. Results indicate that a hydroxyl group in the central region is crucial for the potency as well as the spatial distribution of the hydrophobic portion. Docking studies revealed a similar interaction of the classical HO-1 inhibitors with the active site of the protein. The most potent and selective compound (

Indexed as

Antineoplastic AgentsBreast NeoplasmsCell Line, TumorCell ProliferationCell SurvivalFemaleGene Expression Regulation, NeoplasticHeme Oxygenase-1HumansImidazolesMCF-7 CellsMolecular Docking SimulationMolecular StructureAntineoplastic AgentsHeme Oxygenase-1HMOX1 protein, humanImidazolesanticancerheme oxygenaseHO-1imidazoleinhibitorsstructure–activity relationships

Identifiers

PMID32168943
PMCPMC7139504

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.