Evidence map›Paper›PMID 32335943›Full record

ArticleEnvironmental toxicology and chemistry2020

In Silico Identification of Chemicals Capable of Binding to the Ecdysone Receptor.

Claire L Mellor, Knut Erik Tollefsen, Carlie LaLone, Mark T D Cronin, James W Firman

Open access · hybridAbstract read
In one paragraph

Article in Environmental toxicology and chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Prioritising research on endocrine disruption in the marine environment: a global perspective.Biological reviews of the Cambridge Philosophical Society · 2026
    Review
  2. Review
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

5 authors at 4 institutions in 3 countries.

Claire L MellorSchool of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom.
Knut Erik TollefsenNorwegian Institute for Water Research, Oslo, Norway.
Carlie LaLoneGreat Lakes Toxicology and Ecology Division, Center for Computational Toxicology and Exposure, Office of Research and Development, US Environmental Protection Agency, Duluth, Minnesota, USA.ORCID 0000-0003-3174-1314
Mark T D CroninSchool of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom.
James W FirmanSchool of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom.ORCID 0000-0003-0319-1407
Liverpool John Moores University · GBEnvironmental Protection Agency · USNorwegian Institute for Water Research · NOUniversity of Lancashire · GB

Funding

Intramural EPA EPA999999Norges Forskningsråd NFR-221455
6 · The paper itself

Abstract

The process of molting, known alternatively as ecdysis, is a feature integral in the life cycles of species across the arthropod phylum. Regulation occurs as a function of the interaction of ecdysteroid hormones with the arthropod nuclear ecdysone receptor-a process preceding the triggering of a series of downstream events constituting an endocrine signaling pathway highly conserved throughout environmentally prevalent insect, crustacean, and myriapod organisms. Inappropriate ecdysone receptor binding and activation forms the essential molecular initiating event within possible adverse outcome pathways relating abnormal molting to mortality in arthropods. Definition of the characteristics of chemicals liable to stimulate such activity has the potential to be of great utility in mitigation of hazards posed toward vulnerable species. Thus the aim of the present study was to develop a series of rule-sets, derived from the key structural and physicochemical features associated with identified ecdysone receptor ligands, enabling construction of Konstanz Information Miner (KNIME) workflows permitting the flagging of compounds predisposed to binding at the site. Data describing the activities of 555 distinct chemicals were recovered from a variety of assays across 10 insect species, allowing for formulation of KNIME screens for potential binding activity at the molecular initiating event and adverse outcome level of biological organization. Environ Toxicol Chem 2020;39:1438-1450. © 2020 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

Indexed as

Computer SimulationAdverse Outcome PathwaysAminopyrineAnimalsChloramphenicolEcdysoneEcdysteroneEcotoxicologyLigandsPhthalazinesProtein BindingPyridinesReceptors, SteroidReproducibility of ResultsSpecies SpecificityAminopyrineChloramphenicolEcdysoneecdysone receptorEcdysteroneLigandsPhthalazinesPyridinesReceptors, SteroidvatalanibArthropodComputational toxicologyEcdysone receptorEndocrine-disrupting compoundsInvertebrate toxicology

Identifiers

PMID32335943
PMCPMC7781155
OpenAlexW3018768920

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.