Evidence map›Paper›PMID 31588734›Full record

ArticleACS infectious diseases2019

Ureadepsipeptides as ClpP Activators.

Elizabeth C Griffith, Ying Zhao, Aman P Singh, Brian P Conlon, Rajendra Tangallapally, William R Shadrick, Jiuyu Liu, Miranda J Wallace, Lei Yang, John M Elmore and 8 more

Open access · greenAbstract read
In one paragraph

Article in ACS infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Fighting Antimicrobial Resistance: Innovative Drugs in Antibacterial Research.Angewandte Chemie (International ed. in English) · 2025
    Review
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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

18 authors at 2 institutions in 1 country.

Elizabeth C GriffithDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Ying ZhaoDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Aman P SinghDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Brian P ConlonAntimicrobial Discovery Center, Department of Biology , Northeastern University , 360 Huntington Avenue , Boston , Massachusetts 02115 , United States.
Rajendra TangallapallyDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
William R ShadrickDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Jiuyu LiuDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Miranda J WallaceDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Lei YangDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
John M ElmoreDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Yong LiDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Zhong ZhengDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Darcie J MillerDepartment of Structure Biology , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Martin N CheramieDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Robin B LeeDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.
Michael D LaFleurArietis Pharma , 650 Albany Street, Suite 114 , Boston , Massachusetts 02118 , United States.
Kim LewisAntimicrobial Discovery Center, Department of Biology , Northeastern University , 360 Huntington Avenue , Boston , Massachusetts 02115 , United States.
Richard E LeeDepartment of Chemical Biology and Therapeutics , St. Jude Children's Research Hospital , 262 Danny Thomas Place , Memphis , Tennessee 38105 , United States.ORCID 0000-0002-2397-0443
St. Jude Children's Research Hospital · USNortheastern University · US

Funding

Development of ureadepsipetides for drug-resistant infectionsR01AI141193 · NIAID · ARIETIS · PI LAFLEUR, MICHAEL, LEE, RICHARD E. · 2019 to 2023
$6.4M
Developing therapeutics to treat chronic infectionsR01AI110578 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI LEE, RICHARD E., LEWIS, KIM · 2014 to 2018
$3.8M
Bactericidal antibiotic for Vancomycin Resistant EnterococciR44AI122426 · NIAID · ARIETIS · PI LAFLEUR, MICHAEL · 2016 to 2018
$3.7M
Therapy Against Recalcitrant C. albicans InfectionR44AI074258 · NIAID · ARIETIS · PI DAHL, THOMAS A · 2010 to 2012
$3.0M
NIAID NIH HHS R01 AI110578NIAID NIH HHS R01 AI141193NIAID NIH HHS R44 AI074258NIAID NIH HHS R44 AI122426
6 · The paper itself

Abstract

Acyldepsipeptides are a unique class of antibiotics that act via allosterically dysregulated activation of the bacterial caseinolytic protease (ClpP). The ability of ClpP activators to kill nongrowing bacteria represents a new opportunity to combat deep-seated biofilm infections. However, the acyldepsipeptide scaffold is subject to rapid metabolism. Herein, we explore alteration of the potentially metabolically reactive α,β unsaturated acyl chain. Through targeted synthesis, a new class of phenyl urea substituted depsipeptide ClpP activators with improved metabolic stability is described. The ureadepsipeptides are potent activators of

Indexed as

Anti-Bacterial AgentsBacterial ProteinsDepsipeptidesEndopeptidase ClpEnzyme ActivatorsProtein DomainsStaphylococcus aureusUreaAnti-Bacterial AgentsBacterial ProteinsDepsipeptidesEndopeptidase ClpEnzyme ActivatorsUreaacyldepsipeptideantibioticbiofilmClpPureadepsipeptide

Identifiers

PMID31588734
PMCPMC6916429
OpenAlexW2979503636

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.