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Cytotoxic Natural Products from the Jurassic Relict Osmunda regalis L.
Carpinteyro Diaz, Andrea Estefania; Herfindal, Lars; Holmelid, Bjarte; Brede, Cato; Andersen, Heidi Lie; Vedeler, Anni; Fossen, Torgils.
  • Carpinteyro Diaz AE; Department of Chemistry and Centre for Pharmacy, University of Bergen, N-5007 Bergen, Norway.
  • Herfindal L; Department of Clinical Science and Centre for Pharmacy, University of Bergen, N-5009 Bergen, Norway.
  • Holmelid B; Department of Chemistry and Centre for Pharmacy, University of Bergen, N-5007 Bergen, Norway.
  • Brede C; Department of Medical Biochemistry, Stavanger University Hospital, N-4011 Stavanger, Norway.
  • Andersen HL; University Gardens, University of Bergen, Allégt. 41, N-5007 Bergen, Norway.
  • Vedeler A; Department of Biomedicine, University of Bergen, N-5009 Bergen, Norway.
  • Fossen T; Department of Chemistry and Centre for Pharmacy, University of Bergen, N-5007 Bergen, Norway.
Molecules ; 29(17)2024 Sep 07.
Article en En | MEDLINE | ID: mdl-39275095
ABSTRACT
The Jurassic relict Royal fern, Osmunda regalis L., is widely distributed across temperate zones in the Northern and Southern hemispheres. Even though this species has been utilised for centuries as a medicinal plant, its phytochemical composition mainly remains unknown. As part of our ongoing research to identify potential lead compounds for future anticancer drugs, 17 natural products were characterised from the aerial parts of Osmunda regalis L. Fifteen of these compounds were identified in this species for the first time, including the six previously undescribed compounds kaempferol 3-O-(2''-O-(2'''-α-rhamnopyranosyl)-ß-glucopyranosyl)-ß-glucopyranoside, quercetin 3-O-(2''-O-(2'''-α-rhamnopyranosyl)-ß-glucopyranosyl)-ß-glucopyranoside, kaempferol 3-O-(2''-O-(2'''-α-rhamnopyranosyl-6'''-O-(E)-caffeoyl-)-ß-glucopyranosyl)-ß-glucopyranoside, 3-methoxy-5-hydroxy-4-olide, 4-hydroxy-3-(3'-hydroxy-4'-(hydroxyethyl)-oxotetrafuranone-5-methyl tetrahydropyranone, and 4-O-(5-hydroxy-4-oxohexanoyl) osmundalactone. The molecular structures were determined by combining several 1D and 2D NMR experiments, circular dichroism spectroscopy, and HRMS. Determination of cytotoxicity against AML MOLM-13, H9c2, and NRK cell lines showed that two isolated lactones exhibited significant cytotoxic activity.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Productos Biológicos Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Productos Biológicos Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article