Evidence map›Paper›PMID 40901832›Full record

ArticlePloS one2025

Cadinapyridine sesquiterpene alkaloids from Artemisia annua and in vitro cytotoxicity and antiplasmodial activities.

Nicolas Fabre, Adrien Vitrai, Sandra Bourgeade-Delmas, Nathalie Saffon-Merceron, Abdou Madjid Olatoundé Amoussa, Latifou Lagnika, Agnès Aubouy, Valérie Jullian

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Nicolas FabreUMR 152 PharmaDev, Université de Toulouse, UPS, IRD, Toulouse, France.ORCID https://orcid.org/0000-0001-5896-5700
Adrien VitraiUMR 152 PharmaDev, Université de Toulouse, UPS, IRD, Toulouse, France.ORCID https://orcid.org/0009-0008-2256-4866
Sandra Bourgeade-DelmasUMR 152 PharmaDev, Université de Toulouse, UPS, IRD, Toulouse, France.
Nathalie Saffon-MerceronInstitut de Chimie de Toulouse, ICT UAR 2599, Université Paul Sabatier-Toulouse III, Toulouse, France.
Abdou Madjid Olatoundé AmoussaLaboratoire de Biochimie et Substances Naturelles Bioactives (LBSNB), Faculté des Sciences et Techniques (FAST), Université d'Abomey Calavi, Abomey Calavi, Bénin.
Latifou LagnikaLaboratoire de Biochimie et Substances Naturelles Bioactives (LBSNB), Faculté des Sciences et Techniques (FAST), Université d'Abomey Calavi, Abomey Calavi, Bénin.
Agnès AubouyUMR 152 PharmaDev, Université de Toulouse, UPS, IRD, Toulouse, France.
Valérie JullianUMR 152 PharmaDev, Université de Toulouse, UPS, IRD, Toulouse, France.ORCID https://orcid.org/0000-0002-1675-9105

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Artemisia annua L. (A. annua) is a medicinal herb that has been used for the last two millennia to treat various diseases. In African countries, teas prepared from cultivated A. annua have been used to treat malaria for the past three decades. In another work, our team investigated the antiplasmodial efficacy of these traditional preparations using a Liquid-Chromatography-Mass Spectrometry metabolomic approach on various teas prepared from different batches of A. annua collected in Benin and in France and highlighted an original nitrogenous compound. The present work aimed to isolate and characterize its structure. Therefore we describe the fractionation of an alkaloid extract from a Beninese sample of the plant's aerial parts led to the isolation of two previously undescribed alkaloids, annuanine A (1) and annuanine B (2) along with the known fabianine (3), all possessing a very unusual skeleton. Their structures were determined through NMR and MS data analyses. The structure of 1 was further confirmed by single-crystal X-ray structural analysis. Compounds 1 and 2 were evaluated for cell-growth inhibition on Caco-2, VERO, and Thp1 cells, as well as on the Plasmodium falciparum FcB1 strain. Unfortunately, the two compounds 1 and 2 were inactive in these in vitro models. Comparison of LC-HRMS data between annuanine B and A. annua tea allowed us to identify it as the nitrogenous compound highlighted by our previous study. These results enhance the chemical knowledge of this well-known ethnopharmacological herb and highlight a very rare alkaloid skeleton that may have formed from the degradation of artemisinin during plant storage.

Indexed as

AlkaloidsAntimalarialsArtemisia annuaPlasmodium falciparumSesquiterpenesAnimalsCaco-2 CellsChlorocebus aethiopsHumansPlant ExtractsAlkaloidsAntimalarialsPlant ExtractsSesquiterpenes

Identifiers

PMID40901832
PMCPMC12407398

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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.