Evidence map›Paper›PMID 29844038›Full record

ArticleAntimicrobial agents and chemotherapy2018

Antibacterial Spectrum of a Tetrazole-Based Reversible Inhibitor of Serine β-Lactamases.

Orville A Pemberton, Xiujun Zhang, Derek A Nichols, Kyle DeFrees, Priyadarshini Jaishankar, Richard Bonnet, Jessie Adams, Lindsey N Shaw, Adam R Renslo, Yu Chen

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Computational Evaluation ofCurrent computer-aided drug design · 2026
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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 at 3 institutions in 2 countries.

Orville A Pemberton *Department of Molecular Medicine, University of South Florida, Tampa, Florida, USA.
Xiujun Zhang *Department of Molecular Medicine, University of South Florida, Tampa, Florida, USA.
Derek A NicholsDepartment of Molecular Medicine, University of South Florida, Tampa, Florida, USA.
Kyle DeFreesDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, California, USA.
Priyadarshini JaishankarDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, California, USA.
Richard BonnetClermont Université, Université d'Auvergne, INSERM U1071, INRA USC2018, Clermont-Ferrand, France.
Jessie AdamsDepartment of Cell Biology, Microbiology & Molecular Biology, University of South Florida, Tampa, Florida, USA.
Lindsey N ShawDepartment of Cell Biology, Microbiology & Molecular Biology, University of South Florida, Tampa, Florida, USA.ORCID 0000-0002-0629-8990
Adam R RensloDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, California, USA adam.renslo@ucsf.edu ychen1@health.usf.edu.ORCID 0000-0002-1240-2846
Yu ChenDepartment of Molecular Medicine, University of South Florida, Tampa, Florida, USA adam.renslo@ucsf.edu ychen1@health.usf.edu.ORCID 0000-0002-5115-3600
University of South Florida · USUniversity of California, San Francisco · USInserm · FR

Funding

RESEARCH TRAINING IN CHEMISTRY AND CHEMICAL BIOLOGYT32GM064337 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CRAIK, CHARLES SCOTT · 2002 to 2021
$7.8M
Evolution and inhibition of beta-lactamase activity in antibiotic resistanceR01AI103158 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI CHEN, YU · 2013 to 2017
$2.0M
NIAID NIH HHS R01 AI103158NIGMS NIH HHS T32 GM064337
6 · The paper itself

Abstract

CTX-M is the most prevalent family of extended-spectrum β-lactamases. We recently developed a tetrazole-derived noncovalent inhibitor of CTX-M-9. Here, we present the biochemical and microbiological activity of this inhibitor across a representative panel of serine β-lactamases and Gram-negative bacteria. The compound displayed significant activity against all major subgroups of CTX-M, including CTX-M-15, while it exhibited some low-level inhibition of other serine β-lactamases. Complex crystal structures with the CTX-M-14 S237A mutant and CTX-M-27 illustrate the binding contribution of specific active-site residues on the β3 strand.

Indexed as

Anti-Bacterial Agentsbeta-LactamasesGram-Negative BacteriaMicrobial Sensitivity TestsTetrazolesAnti-Bacterial Agentsbeta-LactamasesTetrazolesantibacterialinhibitorβ-lactamase

Identifiers

PMID29844038
PMCPMC6105816
OpenAlexW2804418963

What OpenQuestion holds

Textmetadata
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.