Evidence map›Paper›PMID 30302779›Full record

ReviewDrug development research2019

Microbial esterases and ester prodrugs: An unlikely marriage for combating antibiotic resistance.

Erik M Larsen, R Jeremy Johnson

Open access · greenAbstract readReview
In one paragraph

Review in Drug development research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
  3. A novel approach to combatMicrobiology spectrum · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Prodrug activation in malaria parasites mediated by an imported erythrocyte esterase, acylpeptide hydrolase (APEH).Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Review
  9. Prodrug Approach as a Strategy to Enhance Drug Permeability.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  10. C(spACS catalysis · 2025
    Article
  11. Article
  12. Article
  13. Article
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  18. Article
  19. Fluoroquinolone Derivatives in the Treatment ofPharmaceuticals (Basel, Switzerland) · 2022
    Article
  20. 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

2 authors at 1 institution in 1 country.

Erik M LarsenDepartment of Chemistry and Biochemistry, Butler University, Indianapolis, Indiana.
R Jeremy JohnsonDepartment of Chemistry and Biochemistry, Butler University, Indianapolis, Indiana.ORCID 0000-0003-2694-3915
Butler University · US

Funding

Investigation of mycobacterial hydrolases and their role in lipolysis.R15GM110641 · NIGMS · BUTLER UNIVERSITY · PI JOHNSON, RANDAL JEREMY · 2015 to 2015
$306k
NIGMS NIH HHS NIH 1 R15 GM110641-01A1NIGMS NIH HHS R15 GM110641
6 · The paper itself

Abstract

The rise of antibiotic resistance necessitates the search for new platforms for drug development. Prodrugs are common tools for overcoming drawbacks typically associated with drug formulation and delivery, with ester prodrugs providing a classic strategy for masking polar alcohol and carboxylic acid functionalities and improving cell permeability. Ester prodrugs are normally designed to have simple ester groups, as they are expected to be cleaved and reactivated by a wide spectrum of cellular esterases. However, a number of pathogenic and commensal microbial esterases have been found to possess significant substrate specificity and can play an unexpected role in drug metabolism. Ester protection can also introduce antimicrobial properties into previously nontoxic drugs through alterations in cell permeability or solubility. Finally, mutation to microbial esterases is a novel mechanism for the development of antibiotic resistance. In this review, we highlight the important pathogenic and xenobiotic functions of microbial esterases and discuss the development and application of ester prodrugs for targeting microbial infections and combating antibiotic resistance. Esterases are often overlooked as therapeutic targets. Yet, with the growing need to develop new antibiotics, a thorough understanding of the specificity and function of microbial esterases and their combined action with ester prodrug antibiotics will support the design of future therapeutics.

Indexed as

AnimalsAnti-Bacterial AgentsDrug Resistance, MicrobialEsterasesEstersHumansProdrugsProtein Structure, SecondaryProtein Structure, TertiaryAnti-Bacterial AgentsEsterasesEstersProdrugsantibiotic resistancedrug deliverydrug designesterasesMycobacterium tuberculosisprodrugs

Identifiers

PMID30302779
PMCPMC6377847
OpenAlexW2896971423

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.