<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-14T14:15:05Z</responseDate><request verb="GetRecord" identifier="oai:gredos.usal.es:10366/168760" metadataPrefix="mods">https://gredos.usal.es/oai/request</request><GetRecord><record><header><identifier>oai:gredos.usal.es:10366/168760</identifier><datestamp>2026-01-15T01:01:47Z</datestamp><setSpec>com_10366_149436</setSpec><setSpec>com_10366_3947</setSpec><setSpec>com_10366_3946</setSpec><setSpec>com_10366_3823</setSpec><setSpec>col_10366_151253</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
<mods:name>
<mods:namePart>Vega, Jennifer de la</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Alejo-Armijo, Alfonso</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Pineda, Laura M.</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>López-Pérez, José Luis</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Ng, Michelle G.</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Larqué, Horacio</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Hernandez, Miriam</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Spadafora, Carmenza</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Olmo Fernández, Esther del</mods:namePart>
</mods:name>
<mods:extension>
<mods:dateAvailable encoding="iso8601">2026-01-14T10:39:34Z</mods:dateAvailable>
</mods:extension>
<mods:extension>
<mods:dateAccessioned encoding="iso8601">2026-01-14T10:39:34Z</mods:dateAccessioned>
</mods:extension>
<mods:originInfo>
<mods:dateIssued encoding="iso8601">2025-04-19</mods:dateIssued>
</mods:originInfo>
<mods:identifier type="issn">0378-8741</mods:identifier>
<mods:identifier type="uri">http://hdl.handle.net/10366/168760</mods:identifier>
<mods:identifier type="doi">10.1016/j.jep.2025.119840</mods:identifier>
<mods:abstract>Ethnopharmacological relevance: Medicinal plants are rich in bioactive compounds with diverse properties that can&#xd;
preserve human health. Eryngium bourgatii is used in traditional medicine to purify the blood. Species of this&#xd;
genus have been used for their antibacterial, antitumor, antifungal or antiparasitic properties among others.&#xd;
Aim of the study: In this work, the antiparasitic properties against Leishmania donovani, Trypanosoma cruzi, and&#xd;
Plasmodium falciparum were evaluated.&#xd;
Materials and methods: Methyl tert-butyl ether (MTBE), dichloromethane (DCM), and ethyl acetate (EtOAc) extracts&#xd;
of the roots and the non-flowering aerial parts were obtained by maceration at room temperature. Some of&#xd;
them were partitioned with solvents of increasing polarity, specifically n-hexane (n-Hex), dichloromethane&#xd;
(DCM), and ethyl acetate (EA) to isolate different fractions. Growth inhibition assays were performed against the&#xd;
three protozoa (L. donovani, T. cruzi, and P. falciparum). The active fractions were subsequently separated by&#xd;
chromatography to determine the secondary metabolites responsible for the activity. In addition, GC-MS studies&#xd;
were performed to further analyse the composition of the extracts and fractions.&#xd;
Results: Regarding the roots, the MTBE extract was the most potent leishmanicidal (77.7 % inhibition at 10 μg/&#xd;
mL). The activity increased in its n-Hex fraction (95.3 % inhibition), and in the DCM fraction, both leishmanicidal&#xd;
(93.6 %) and anti-Chagas activity (92.2 %) improved. Furanone 12, a new natural compound, was the main&#xd;
component of the extract and the most potent leishmanicide (96.7 %), sixteen times less than the reference drug,&#xd;
Amphotericin B. 11-Acetoxyfalcarindiol (19) was the most potent anti-Chagas (89.1 % inhibition). Regarding the&#xd;
aerial parts, the DCM extract was the most potent leishmanicide (83.3 %), which improved in its DCM fraction&#xd;
(95.7 %), mainly attributed to compound 12. The DCM fraction of the MTBE extract produced the best antichagasic&#xd;
result (93.3 % inhibition), attributed to falcarindiol (17). Practically, the same compounds were&#xd;
identified in the roots as in the aerial parts, but in different proportions. Nine pure compounds were isolated; 34&#xd;
were identified in roots and 37 in the aerial parts by GC-MS, with alkyne compounds leading, followed by&#xd;
sesquiterpenes and fatty acids.</mods:abstract>
<mods:language>
<mods:languageTerm>eng</mods:languageTerm>
</mods:language>
<mods:accessCondition type="useAndReproduction">info:eu-repo/semantics/embargoedAccess</mods:accessCondition>
<mods:subject>
<mods:topic>Eryngium bourgatii. Structural characterization. Acetylenes. Leishmanicidal. Trypanocidal. Anti-plasmodial activity</mods:topic>
</mods:subject>
<mods:titleInfo>
<mods:title>Antiparasitic activity of Eryngium bourgatii Gouan: Fractionation and isolation of constituents from roots and aerial parts</mods:title>
</mods:titleInfo>
<mods:genre>info:eu-repo/semantics/article</mods:genre>
</mods:mods></metadata></record></GetRecord></OAI-PMH>