Evidence map›Paper›PMID 28343384›Full record

ArticleACS infectious diseases2017

N6', N6''', and O4' Modifications to Neomycin Affect Ribosomal Selectivity without Compromising Antibacterial Activity.

Girish C Sati, Dimitri Shcherbakov, Sven N Hobbie, Andrea Vasella, Erik C Böttger, David Crich

Abstract read
In one paragraph

Article in ACS infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Phenotypic Differentiation Within theAntibiotics (Basel, Switzerland) · 2024
    Article
  3. Facile and selectiveGreen chemistry : an international journal and green chemistry resource : GC · 2022
    Article
  4. Article
  5. Dissociating antibacterial from ototoxic effects of gentamicin C-subtypes.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. 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

6 authors at 3 institutions in 2 countries.

Girish C SatiDepartment of Chemistry, Wayne State University , Detroit, Michigan 48202, United States.
Dimitri ShcherbakovInstitute of Medical Microbiology, University of Zurich , 8006 Zurich, Switzerland.
Sven N HobbieInstitute of Medical Microbiology, University of Zurich , 8006 Zurich, Switzerland.
Andrea VasellaOrganic Chemistry Laboratory, ETH Zurich , 8093 Zurich, Switzerland.
Erik C BöttgerInstitute of Medical Microbiology, University of Zurich , 8006 Zurich, Switzerland.
David CrichDepartment of Chemistry, Wayne State University , Detroit, Michigan 48202, United States.ORCID 0000-0003-2400-0083
University of Zurich · CHWayne State University · USETH Zurich · CH

Funding

Shaping Next Generation Aminoglycoside Antibiotics for Treatment of Multidrug-Resistant DiseasesR01AI123352 · NIAID · WAYNE STATE UNIVERSITY · PI CRICH, DAVID · 2016 to 2019
$2.7M
NIAID NIH HHS R01 AI123352
6 · The paper itself

Abstract

The synthesis of a series of neomycin derivatives carrying the 2-hydroxyethyl substituent on N6' and/or N6‴ both alone and in combination with a 4'-O-ethyl group is described. By means of cell-free translation assays with wild-type bacterial ribosomes and their hybrids with eukaryotic decoding A sites, we investigate how individual substituents and their combinations affect activity and selectivity at the target level. In principle, and as shown by cell-free translation assays, modifications of the N6' and N6‴ positions allow enhancement of target selectivity without compromising antibacterial activity. As with the 6'OH aminoglycoside paromomycin, the 4'-O-ethyl modification affects the ribosomal activity, selectivity, and antibacterial profile of neomycin and its 6'-N-(2-hydroxyethyl) derivatives. The modified aminoglycosides show good antibacterial activity against model Gram-positive and Gram-negative microbes including the ESKAPE pathogens Staphylococcus aureus, Klebsiella pneumoniae, Enterobacter cloacae, and Acinetobacter baumannii.

Indexed as

Acinetobacter baumanniiAnti-Bacterial AgentsBase PairingBase SequenceCarbohydrate ConformationEnterobacter cloacaeKlebsiella pneumoniaeMicrobial Sensitivity TestsNeomycinParomomycinProtein BiosynthesisRibosomesStaphylococcus aureusStructure-Activity RelationshipSubcellular FractionsAnti-Bacterial AgentsNeomycinParomomycinaminoglycosidescell-free translation assaydecoding A sitemultidrug-resistant infectious diseasesototoxicitysynthesis

Identifiers

PMID28343384
PMCPMC5526222
OpenAlexW2597546519

What OpenQuestion holds

Textmetadata
LicenceTDM
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.