Evidence map›Paper›PMID 36194525›Full record

ArticleChemMedChem2022

Effects of Structural Variations on Antibacterial Properties for Conjugated Diynes Generated through Glaser Hay Couplings.

Emma A Hale, Hannah M Ryan, Alexandra M McOsker, Cody M Funk, Lauren C Green, Lauren E Mazur, Diya M Uthappa, Brian M Flood, Douglas D Young, Robert J Hinkle

Abstract read
In one paragraph

Article in ChemMedChem, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Emma A HaleDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.
Hannah M RyanDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.
Alexandra M McOskerDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.
Cody M FunkDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.
Lauren C GreenDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.
Lauren E MazurDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.
Diya M UthappaDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.
Brian M FloodDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.
Douglas D YoungDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.ORCID 0000-0003-4433-4101
Robert J HinkleDepartment of Chemistry, William & Mary, PO Box 8795, Williamsburg, VA, 23187, USA.ORCID 0000-0001-5042-5670

Funding

EPA EP-D-17-020
6 · The paper itself

Abstract

Antibiotic resistance is a growing problem facing global societies today. Many new antibiotics are derivatized versions of already existing antibiotics, which allows for antibiotic resistance to arise. To combat this issue, new antibiotics with different core structures need to be elucidated. Asymmetrical polyacetylenes have been isolated from natural products and they have previously been demonstrated to exhibit antimicrobial and antibacterial activity; however, their synthetic preparation has not made them easily amenable to rapid derivatization for SAR studies. Using a combination of solution and solid-supported chemistries, an array of diynes inspired by a known natural product were prepared and assessed for antibacterial activity. Ultimately, several compounds were identified with improved activity in bacterial viability assays. Moreover, some compounds were discovered that displayed a degree of specificity for E. coli over P. fluorescens and vice versa. These new compounds show promise, and further investigation is needed to pinpoint the specific structural components that elicit biological activity.

Indexed as

Biological ProductsDiynesAnti-Bacterial AgentsEscherichia coliMicrobial Sensitivity TestsPolyynesAnti-Bacterial AgentsBiological ProductsDiynesPolyynesdiyneE. coliGlaser HayP. fluorescenspolyynestructure-activity relationship

Identifiers

PMID36194525
PMCPMC10092682

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.