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dc.contributor.authorCarpinteyro Diaz, Andrea Estefania
dc.contributor.authorHerfindal, Lars
dc.contributor.authorAndersen, Heidi Lie
dc.contributor.authorFossen, Torgils
dc.date.accessioned2024-03-26T13:53:04Z
dc.date.available2024-03-26T13:53:04Z
dc.date.created2024-01-08T13:48:14Z
dc.date.issued2023
dc.identifier.issn1431-5157
dc.identifier.urihttps://hdl.handle.net/11250/3124267
dc.description.abstractParsley fern, Cryptogramma crispa, is a common fern in arctic–alpine regions, and even though this species has been known since ancient times and has been presumed to cause the poisoning of horses, its natural products have not previously been investigated. Here, we characterise 15 natural products isolated from the aerial parts of Cryptogramma crispa, including the previously undescribed compound 3-malonyl pteroside D. The structure determinations were based on several advanced 1D and 2D NMR spectroscopic techniques, Circular Dichroism spectroscopy and high-resolution mass spectrometry. The pteroside derivatives exhibited selective moderate cytotoxic activity against the acute myeloid leukaemia MOLM13 cell line and no cytotoxicity against the normal heart and kidney cell lines, suggesting that their potential anticancer effect should be further investigated.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleCytotoxic Natural Products Isolated from Cryptogramma crispa (L.) R. Br.en_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.source.articlenumber7723en_US
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1
dc.identifier.doi10.3390/molecules28237723
dc.identifier.cristin2222365
dc.source.journalMoleculesen_US
dc.identifier.citationMolecules. 2023, 28 (23), 7723.en_US
dc.source.volume28en_US
dc.source.issue23en_US


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