Evidence map›Paper›PMID 24236721›Full record

ReviewCurrent topics in medicinal chemistry2014

Progress in the discovery of treatments for C. difficile infection: A clinical and medicinal chemistry review.

Lissa S Tsutsumi, Yaw B Owusu, Julian G Hurdle, Dianqing Sun

Open access · bronzeAbstract readReview
In one paragraph

Review in Current topics in medicinal chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Small-Molecule Inhibition of theACS chemical biology · 2019
    Article
  6. Recent advances in the treatment ofInfection and drug resistance · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Clinical interventions in aging · 2017
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Resistance-resistant antibiotics.Trends in pharmacological sciences · 2014
    Review
  18. 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

4 authors at 2 institutions in 1 country.

Lissa S Tsutsumi
Yaw B Owusu
Julian G Hurdle
Dianqing SunDepartment of Pharmaceutical Sciences, The Daniel K. Inouye College of Pharmacy, University of Hawai'i at Hilo, 34 Rainbow Drive, Hilo, HI 96720, USA. dianqing@hawaii.edu.
University of Hawaii at Hilo · USThe University of Texas at Arlington · US

Funding

UH Hilo COP A&RP20GM103466 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI Peter R Hoffmann · 2012 to 2026
$60.3M
USING EEG COMPLEXITY AND HIGH PERFORMANCE COMPUTING TO PROFILE SLEEPP20RR016467 · NCRR · UNIVERSITY OF HAWAII AT MANOA · PI HOLMES, ERIC · 2001 to 2011
$24.5M
Nature inspired treatments for persistent C. difficile infectionsR01AT006732 · NCCIH · UNIVERSITY OF TEXAS ARLINGTON · PI HURDLE, JULIAN G · 2011 to 2015
$1.9M
Development of Piperidinols and Engelhardiones as Novel Antituberculosis AgentsR15AI092315 · NIAID · UNIVERSITY OF HAWAII AT HILO · PI SUN, DIANQING · 2011 to 2011
$406k
NCCIH NIH HHS 5R01AT006732NCCIH NIH HHS R01 AT006732NCRR NIH HHS P20 RR016467NCRR NIH HHS P20RR016467NIAID NIH HHS R15 AI092315NIAID NIH HHS R15AI092315NIGMS NIH HHS P20 GM103466NIGMS NIH HHS P20GM103466
6 · The paper itself

Abstract

Clostridium difficile is an anaerobic, Gram-positive pathogen that causes C. difficile infection, which results in significant morbidity and mortality. The incidence of C. difficile infection in developed countries has become increasingly high due to the emergence of newer epidemic strains, a growing elderly population, extensive use of broad spectrum antibiotics, and limited therapies for this diarrheal disease. Because treatment options currently available for C. difficile infection have some drawbacks, including cost, promotion of resistance, and selectivity problems, new agents are urgently needed to address these challenges. This review article focuses on two parts: the first part summarizes current clinical treatment strategies and agents under clinical development for C. difficile infection; the second part reviews newly reported anti-difficile agents that have been evaluated or reevaluated in the last five years and are in the early stages of drug discovery and development. Antibiotics are divided into natural product inspired and synthetic small molecule compounds that may have the potential to be more efficacious than currently approved treatments. This includes potency, selectivity, reduced cytotoxicity, and novel modes of action to prevent resistance.

Indexed as

Anti-Bacterial AgentsClostridioides difficileEnterocolitis, PseudomembranousHumansAnti-Bacterial Agents

Identifiers

PMID24236721
PMCPMC3921470
OpenAlexW2098638379

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.