Evidence map›Paper›PMID 33630860›Full record

ArticlePloS one2021

Metabolite profile of Nectandra oppositifolia Nees & Mart. and assessment of antitrypanosomal activity of bioactive compounds through efficiency analyses.

Geanne A Alves Conserva, Luis M Quirós-Guerrero, Thais A Costa-Silva, Laurence Marcourt, Erika G Pinto, Andre G Tempone, João Paulo S Fernandes, Jean-Luc Wolfender, Emerson F Queiroz, João Henrique G Lago

Abstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Anti-Neuroinflammatory Potential of aAntioxidants (Basel, Switzerland) · 2023
    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

10 authors.

Geanne A Alves ConservaCenter of Natural Sciences and Humanities, Federal University of ABC, Santo Andre, Sao Paulo, Brazil.
Luis M Quirós-GuerreroSchool of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
Thais A Costa-SilvaCenter of Natural Sciences and Humanities, Federal University of ABC, Santo Andre, Sao Paulo, Brazil.
Laurence MarcourtSchool of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
Erika G PintoDrug Discovery Unit, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Andre G TemponeCentre for Parasitology and Mycology, Adolfo Lutz Institute, São Paulo, Brazil.
João Paulo S FernandesDepartment of Pharmaceutical Sciences, Federal University of São Paulo, Diadema, São Paulo, Brazil.
Jean-Luc WolfenderSchool of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
Emerson F QueirozSchool of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
João Henrique G LagoCenter of Natural Sciences and Humanities, Federal University of ABC, Santo Andre, Sao Paulo, Brazil.ORCID 0000-0002-1193-8374

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EtOH extracts from the leaves and twigs of Nectandra oppositifolia Nees & Mart. shown activity against amastigote forms of Trypanosoma cruzi. These extracts were subjected to successive liquid-liquid partitioning to afford bioactive CH2Cl2 fractions. UHPLC-TOF-HRMS/MS and molecular networking were used to obtain an overview of the phytochemical composition of these active fractions. Aiming to isolate the active compounds, both CH2Cl2 fractions were subjected to fractionation using medium pressure chromatography combined with semi-preparative HPLC-UV. Using this approach, twelve compounds (1-12) were isolated and identified by NMR and HRMS analysis. Several isolated compounds displayed activity against the amastigote forms of T. cruzi, especially ethyl protocatechuate (7) with EC50 value of 18.1 μM, similar to positive control benznidazole (18.7 μM). Considering the potential of compound 7, protocatechuic acid and its respective methyl (7a), n-propyl (7b), n-butyl (7c), n-pentyl (7d), and n-hexyl (7e) esters were tested. Regarding antitrypanosomal activity, protocatechuic acid and compound 7a were inactive, while 7b-7e exhibited EC50 values from 20.4 to 11.7 μM, without cytotoxicity to mammalian cells. These results suggest that lipophilicity and molecular complexity play an important role in the activity while efficiency analysis indicates that the natural compound 7 is a promising prototype for further modifications to obtain compounds effective against the intracellular forms of T. cruzi.

Indexed as

AnimalsAntiprotozoal AgentsCell LineChagas DiseaseFemaleLauraceaeMiceMice, Inbred BALB CPhytochemicalsPlant ExtractsPlant LeavesTrypanocidal AgentsTrypanosoma cruziAntiprotozoal AgentsPhytochemicalsPlant ExtractsTrypanocidal Agents

Identifiers

PMID33630860
PMCPMC7906415

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Registered trials

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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.