Evidence map›Paper›PMID 27663549›Full record

ArticleBioorganic & medicinal chemistry2016

Identification of 5,6-dihydroimidazo[2,1-b]thiazoles as a new class of antimicrobial agents.

Yangmei Li, Nina Bionda, Renee Fleeman, Hongjie Wang, Akihiko Ozawa, Richard A Houghten, Lindsey Shaw

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2016. 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
0.7field-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

3 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  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

7 authors at 2 institutions in 1 country.

Yangmei LiTorrey Pines Institute for Molecular Studies, 11350 SW Village Parkway, Port St. Lucie, FL 34987, United States. Electronic address: yli@tpims.org.
Nina BiondaTorrey Pines Institute for Molecular Studies, 11350 SW Village Parkway, Port St. Lucie, FL 34987, United States.
Renee FleemanDepartment of Cell Biology, Microbiology and Molecular Biology, University of South Florida, 4202 East Fowler Avenue, Tampa, FL 33620, United States.
Hongjie WangTorrey Pines Institute for Molecular Studies, 11350 SW Village Parkway, Port St. Lucie, FL 34987, United States.
Akihiko OzawaTorrey Pines Institute for Molecular Studies, 11350 SW Village Parkway, Port St. Lucie, FL 34987, United States.
Richard A HoughtenTorrey Pines Institute for Molecular Studies, 11350 SW Village Parkway, Port St. Lucie, FL 34987, United States.
Lindsey ShawDepartment of Cell Biology, Microbiology and Molecular Biology, University of South Florida, 4202 East Fowler Avenue, Tampa, FL 33620, United States.
Torrey Pines Institute For Molecular Studies · USUniversity of South Florida · US

Funding

Characterization of ??S in the stress & virulence responses of S. aureusR01AI080626 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI SHAW, LINDSEY NEIL · 2010 to 2013
$1.3M
Posttranslational regulation of augurin, a new secretory tumor suppressorR21NS075602 · NINDS · TORREY PINES INST FOR MOLECULAR STUDIES · PI OZAWA, AKIHIKO · 2013 to 2014
$474k
Bioprospecting antibiotics in the fungal secondary metabolomeR21AI103715 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI BAKER, BILL J, SHAW, LINDSEY NEIL · 2013 to 2014
$391k
NIAID NIH HHS R01 AI080626NIAID NIH HHS R21 AI103715NINDS NIH HHS R21 NS075602
6 · The paper itself

Abstract

In an effort to develop novel antimicrobial agents against drug-resistant bacterial infections, 5,6-dihydroimidazo[2,1-b]thiazole compounds were synthesized and tested for their antimicrobial activity. Eight compounds comprised by two sub-scaffolds were identified as hits against methicillin-resistant Staphylococcus aureus (MRSA). These hits were modified at 6-position by replacing (S)-6 to (R)-6 configuration and the (R)-isomers increased their antimicrobial activities by two-fold. The most active compound showed a MIC

Indexed as

AnimalsAnti-Bacterial AgentsCell SurvivalDNA GyraseDose-Response Relationship, DrugHEK293 CellsHumansImidazolesMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsMolecular StructureMothsStructure-Activity RelationshipThiazolesTopoisomerase II InhibitorsAnti-Bacterial AgentsDNA GyraseImidazolesThiazolesTopoisomerase II InhibitorsAntimicrobialDNA gyraseHeterocyclicImidazothiazoleMRSA

Identifiers

PMID27663549
PMCPMC5065789
OpenAlexW2518954951

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.