Evidence map›Paper›PMID 26144346›Full record

ArticleBioorganic & medicinal chemistry letters2015

Exploration of the structure-activity relationship of 1,2,4-oxadiazole antibiotics.

Derong Ding, Marc A Boudreau, Erika Leemans, Edward Spink, Takao Yamaguchi, Sebastian A Testero, Peter I O'Daniel, Elena Lastochkin, Mayland Chang, Shahriar Mobashery

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2015. 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
–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

15 citing papers in PubMed.

  1. Article
  2. A Potent and Narrow-Spectrum Antibacterial againstJournal of medicinal chemistry · 2023
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Unconventional Antibacterials and Adjuvants.Accounts of chemical research · 2021
    Article
  8. Article
  9. Review
  10. Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. The oxadiazole antibacterials.Current opinion in microbiology · 2016
    Review
  15. 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

10 authors.

Derong DingDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Marc A BoudreauDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Erika LeemansDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Edward SpinkDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Takao YamaguchiDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Sebastian A TesteroDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Peter I O'DanielDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Elena LastochkinDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Mayland ChangDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.
Shahriar MobasheryDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA. Electronic address: mobashery@nd.edu.

Funding

Novel oxadiazols for the treatment of drug-resistant gram-positive bacteriaR01AI090818 · NIAID · UNIVERSITY OF NOTRE DAME · PI CHANG, MAYLAND F, MOBASHERY, SHAHRIAR · 2010 to 2014
$5.0M
NIAID NIH HHS AI090818NIAID NIH HHS R01 AI090818
6 · The paper itself

Abstract

We have recently disclosed the discovery of the class of 1,2,4-oxadiazole antibiotics, which emerged from in silico docking and scoring efforts. This class of antibacterials exhibits Gram-positive activity, particularly against Staphylococcus aureus. We define the structure-activity relationship (SAR) of this class of antibiotics with the synthesis and evaluation of a series of 59 derivatives with variations in the C ring or C and D rings. A total of 17 compounds showed activity against S. aureus. Four derivatives were evaluated against a panel of 16 Gram-positive strains, inclusive of several methicillin-resistant S. aureus strains. These compounds are broadly active against Gram-positive bacteria.

Indexed as

Anti-Bacterial AgentsDose-Response Relationship, DrugGram-Positive BacteriaMicrobial Sensitivity TestsMolecular StructureOxadiazolesStructure-Activity RelationshipAnti-Bacterial AgentsOxadiazoles1,2,4-OxadiazolesAntibioticsStructure–activity relationship

Identifiers

PMID26144346
PMCPMC4607640

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.