Evidence map›Paper›PMID 35709310›Full record

ArticlePest management science2022

Evaluation of the phytotoxic and antifungal activity of C

David M Cárdenas, Joanna Bajsa-Hirschel, Charles L Cantrell, Carlos Rial, Rosa M Varela, José M G Molinillo, Francisco A Macías

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Pest management science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Exploring Sesquiterpene Lactones fromPlants (Basel, Switzerland) · 2025
    Article
  2. Article
  3. 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

7 authors at 2 institutions in 2 countries.

David M CárdenasAllelopathy Group, Department of Organic Chemistry, Institute of Biomolecules (INBIO), Campus CEIA3, School of Science, University of Cadiz, Cádiz, Spain.
Joanna Bajsa-HirschelNatural Products Utilization Research Unit, United States Department of Agriculture, Agricultural Research Service, University, Oxford, MS, USA.
Charles L CantrellNatural Products Utilization Research Unit, United States Department of Agriculture, Agricultural Research Service, University, Oxford, MS, USA.
Carlos RialAllelopathy Group, Department of Organic Chemistry, Institute of Biomolecules (INBIO), Campus CEIA3, School of Science, University of Cadiz, Cádiz, Spain.ORCID https://orcid.org/0000-0002-0265-9584
Rosa M VarelaAllelopathy Group, Department of Organic Chemistry, Institute of Biomolecules (INBIO), Campus CEIA3, School of Science, University of Cadiz, Cádiz, Spain.ORCID https://orcid.org/0000-0003-3616-9134
José M G MolinilloAllelopathy Group, Department of Organic Chemistry, Institute of Biomolecules (INBIO), Campus CEIA3, School of Science, University of Cadiz, Cádiz, Spain.ORCID https://orcid.org/0000-0002-7844-9401
Francisco A MacíasAllelopathy Group, Department of Organic Chemistry, Institute of Biomolecules (INBIO), Campus CEIA3, School of Science, University of Cadiz, Cádiz, Spain.ORCID https://orcid.org/0000-0001-8862-2864
Universidad de Cádiz · ESAgricultural Research Service · US

Funding

Ministerio de Economía, Industria y Competitividad PID2020-11574RB-I00Ministerio de Economía, Industria y Competitividad, Gobierno de España
6 · The paper itself

Abstract

backgroundNatural products are a promising source for the development of new pesticides with alternative mechanisms of action. In this study, we evaluated the phytotoxic and antifungal activity of a novel family of natural C

resultsMany tested compounds exhibited a strong phytotoxic activity. Lappalone and pertyolide B were the most potent molecules from the tested group. Lappalone displayed a strong inhibition profile against selected weed species, reaching a half-maximal inhibitory concentration (IC

conclusionThe bioassays revealed that frequently the presence of the α-methylene-γ-butyrolactone system is not essential for the bioactivities of sesquiterpene lactones, and suggest that C

Indexed as

AlkaloidsAmaranthusEchinochloaSesquiterpenesAntifungal AgentsBiological Control AgentsAlkaloidsAntifungal AgentsBiological Control AgentsSesquiterpenesC17-sesquiterpenoidsnatural productspest controlpesticide

Identifiers

PMID35709310
PMCPMC9540635
OpenAlexW4282979016

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.