Evidence map›Paper›PMID 33573283›Full record

ArticleInternational journal of molecular sciences2021

Pseudo-Dipeptide Bearing α,α-Difluoromethyl Ketone Moiety as Electrophilic Warhead with Activity against Coronaviruses.

Andrea Citarella, Davide Gentile, Antonio Rescifina, Anna Piperno, Barbara Mognetti, Giorgio Gribaudo, Maria Teresa Sciortino, Wolfgang Holzer, Vittorio Pace, Nicola Micale

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.1field-weighted citation impact, top 5% of its field
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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  6. Review
  7. Progress of the "Molecular Informatics" Section in 2022.International journal of molecular sciences · 2023
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. The New GenerationMicroorganisms · 2021
    Article
  14. Article
  15. SARS-CoV-2 MBiomolecules · 2021
    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

10 authors at 4 institutions in 2 countries.

Andrea CitarellaDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, V.le F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0001-5881-7142
Davide GentileDepartment of Drug Sciences, University of Catania, V.le A. Doria, 95125 Catania, Italy.
Antonio RescifinaDepartment of Drug Sciences, University of Catania, V.le A. Doria, 95125 Catania, Italy.ORCID 0000-0001-5039-2151
Anna PipernoDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, V.le F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0001-6004-5196
Barbara MognettiDepartment of Life Sciences and Systems Biology, University of Torino, Via Accademia Albertina 13, 10123 Torino, Italy.ORCID 0000-0003-2888-8999
Giorgio GribaudoDepartment of Life Sciences and Systems Biology, University of Torino, Via Accademia Albertina 13, 10123 Torino, Italy.ORCID 0000-0002-1583-9146
Maria Teresa SciortinoDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, V.le F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0002-8519-7724
Wolfgang HolzerDepartment of Pharmaceutical Chemistry, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria.
Vittorio PaceDepartment of Pharmaceutical Chemistry, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria.ORCID 0000-0003-3037-5930
Nicola MicaleDepartment of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, V.le F. Stagno d'Alcontres 31, 98166 Messina, Italy.ORCID 0000-0002-9294-6033
University of Messina · ITAccademia Albertina delle Belle Arti · ITUniversity of Catania · ITUniversity of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis of α-fluorinated methyl ketones has always been challenging. New methods based on the homologation chemistry via nucleophilic halocarbenoid transfer, carried out recently in our labs, allowed us to design and synthesize a target-directed dipeptidyl α,α-difluoromethyl ketone (DFMK)

Indexed as

A549 CellsAntiviral AgentsBinding SitesCell LineCoronavirus 229E, HumanCoronavirus M ProteinsCOVID-19DipeptidesHumansKetonesMolecular Docking SimulationMolecular Dynamics SimulationSARS-CoV-2ThermodynamicsViral Matrix ProteinsVirus ReplicationAntiviral AgentsCoronavirus M ProteinsDipeptidesKetonesmembrane protein, SARS-CoV-2Viral Matrix Proteinscoronaviruscysteine proteasesdifluoromethyl ketonehCoV-229ESARS-CoV-2 Mpro

Identifiers

PMID33573283
PMCPMC7866854
OpenAlexW3126589375

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.