Evidence map›Paper›PMID 32652783›Full record

ArticleChemMedChem2020

Synthesis of Antiviral Perfluoroalkyl Derivatives of Teicoplanin and Vancomycin.

Ilona Bereczki, Magdolna Csávás, Zsolt Szűcs, Erzsébet Rőth, Gyula Batta, Eszter Ostorházi, Lieve Naesens, Anikó Borbás, Pál Herczegh

Abstract read
In one paragraph

Article in ChemMedChem, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Teicoplanin-A New Use for an Old Drug in the COVID-19 Era?Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  8. Article
  9. Article
  10. 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

9 authors.

Ilona BereczkiDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, 4032, Debrecen, Hungary.ORCID 0000-0003-4601-7257
Magdolna CsávásDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, 4032, Debrecen, Hungary.ORCID 0000-0002-9329-0689
Zsolt SzűcsDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, 4032, Debrecen, Hungary.ORCID 0000-0001-5548-5349
Erzsébet RőthDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, 4032, Debrecen, Hungary.
Gyula BattaDepartment of Organic Chemistry, University of Debrecen, Egyetem tér 1, 4032, Debrecen, Hungary.ORCID 0000-0002-0442-1828
Eszter OstorháziDepartment of Medical Microbiology, Semmelweis University, Mária u. 41, 1085, Budapest, Hungary.ORCID 0000-0002-9459-7316
Lieve NaesensRega Institute for Medical Research, KU Leuven, 3000, Leuven, Belgium.ORCID 0000-0001-9742-9302
Anikó BorbásDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, 4032, Debrecen, Hungary.ORCID 0000-0001-8462-4547
Pál HerczeghDepartment of Pharmaceutical Chemistry, University of Debrecen, Egyetem tér 1, 4032, Debrecen, Hungary.ORCID 0000-0003-4265-5518

Funding

European Regional Development Fund GINOP-2.3.2-15-2016-00008European Regional Development Fund GINOP-2.3.2-15-2016-00044European Regional Development Fund GINOP-2.3.3-15-2016-00004European Social Fund EFOP-3.6.3-VEKOP-16-2017-00009National Research, Development and Innovation Office of Hungary K119509
6 · The paper itself

Abstract

The limited scope of antiviral drugs and increasing problem of antiviral drug resistance represent a global health threat. Glycopeptide antibiotics and their lipophilic derivatives have emerged as relevant inhibitors of diverse viruses. Herein, we describe a new strategy for the synthesis of dual hydrophobic and lipophobic derivatives of glycopeptides to produce selective antiviral agents without membrane-disrupting activity. Perfluorobutyl and perfluorooctyl moieties were attached through linkers of different length to azido derivatives of vancomycin aglycone and teicoplanin pseudoaglycone, and the new derivatives were evaluated against a diverse panel of viruses. The teicoplanin derivatives displayed strong anti-influenza virus activity at nontoxic concentrations. Some of the perfluoroalkylated glycopeptides were also active against a few other viruses such as herpes simplex virus or coronavirus. These data encourage further exploration of glycopeptide analogues for broad antiviral application.

Indexed as

AnimalsAnti-Bacterial AgentsAntiviral AgentsBacillus subtilisCatalysisCell LineCell SurvivalCoronavirusDogsFluorocarbonsHumansMicrobial Sensitivity TestsPalladiumStaphylococcus aureusStructure-Activity RelationshipTeicoplaninAnti-Bacterial AgentsAntiviral AgentsFluorocarbonsPalladiumTeicoplaninVancomycinantiviralcoronavirusglycopeptide antibioticinfluenza virusperfluoroalkyl

Identifiers

PMID32652783
PMCPMC7540527

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.