Evidence map›Paper›PMID 33049963›Full record

ReviewInternational journal of molecular sciences2020

Amphiphilic Aminoglycosides as Medicinal Agents.

Clément Dezanet, Julie Kempf, Marie-Paule Mingeot-Leclercq, Jean-Luc Décout

Open access · goldAbstract readReview
In one paragraph

Review 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, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Antimicrobial Hydrogel for Diabetic Wound Treatment.International journal of nanomedicine · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Interest of Homodialkyl Neamine Derivatives against ResistantInternational journal of molecular sciences · 2021
    Article
  18. 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

4 authors at 2 institutions in 2 countries.

Clément DezanetMolecular Pharmacochemistry Department, University Grenoble Alpes, CNRS, 470 Rue de la Chimie, F-38000 Grenoble, France.
Julie KempfMolecular Pharmacochemistry Department, University Grenoble Alpes, CNRS, 470 Rue de la Chimie, F-38000 Grenoble, France.
Marie-Paule Mingeot-LeclercqCellular and Molecular Pharmacology Unit, Louvain Drug Research Institute, Catholic University of Louvain, Avenue E. Mounier 73, UCL B1.73.05, 1200 Brussels, Belgium.
Jean-Luc DécoutMolecular Pharmacochemistry Department, University Grenoble Alpes, CNRS, 470 Rue de la Chimie, F-38000 Grenoble, France.ORCID 0000-0001-7058-1304
Centre National de la Recherche Scientifique · FRUCLouvain · BE

Funding

Agence Nationale de la Recherche "Physique et Chimie du Vivant", LABEX ARCANE project no. (ANR-11-LABX-003) and CBH-EUR-GS (ANR-17-EURE-0003)Fondation pour la Recherche Médicale (FRM) post-doctoral grant for JK and CD, DBF20161136768Fonds National de la Recherche Scientifique Belge grants no. 3.4.588.10, 3.4.578.12, T.1003.14, J.0205.16, and T.175.20Indo-French Centre for the Promotion of Advanced Research IFCPAR, project no. 3405-1Région Rhône-Alpes ARC 1, grant no. 12-00887201SATT Linksium Grenoble Alpes Project ANTIGRAM
6 · The paper itself

Abstract

The conjugation of hydrophobic group(s) to the polycationic hydrophilic core of the antibiotic drugs aminoglycosides (AGs), targeting ribosomal RNA, has led to the development of amphiphilic aminoglycosides (AAGs). These drugs exhibit numerous biological effects, including good antibacterial effects against susceptible and multidrug-resistant bacteria due to the targeting of bacterial membranes. In the first part of this review, we summarize our work in identifying and developing broad-spectrum antibacterial AAGs that constitute a new class of antibiotic agents acting on bacterial membranes. The target-shift strongly improves antibiotic activity against bacterial strains that are resistant to the parent AG drugs and to antibiotic drugs of other classes, and renders the emergence of resistant

Indexed as

AminoglycosidesAnti-Bacterial AgentsAntifungal AgentsBacterial Outer MembraneCardiolipinsDrug CarriersDrug Resistance, Multiple, BacterialHydrophobic and Hydrophilic InteractionsLipopolysaccharidesMicrobial Sensitivity TestsPseudomonas aeruginosaSolubilityStructure-Activity RelationshipAminoglycosidesAnti-Bacterial AgentsAntifungal AgentsCardiolipinsDrug CarriersLipopolysaccharidesaminoglycosidesamphiphilicantibacterialantibioticcardiolipindelivery vehicleslipopolysaccharidesmembranes

Identifiers

PMID33049963
PMCPMC7583001
OpenAlexW3091795684

What Socratic 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 Socratic graph.