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Chemical constituents and biological activities of <i>Dianthus elegans</i> var. <i>elegans</i>

Kiymet MutluFaculty of Science, Department of Chemistry, Ege University, Izmir, TurkeyNazlı Böke SarıkahyaFaculty of Science, Department of Chemistry, Ege University, Izmir, TurkeyAyşe NalbantsoyFaculty of Engineering, Department of Bioengineering, Ege University, Izmir, TurkeySüheyla KırmızıgülFaculty of Science, Department of Chemistry, Ege University, Izmir, Turkey
2017en
ABI

Аннотация

Chemical investigation of the aerial parts of Dianthus elegans var. elegans afforded two previously undescribed saponins, named dianosides M-N (1–2), together with four oleanane-type triterpenoid glycosides (3–6). Their structures were elucidated as 3-O-α-L-arabinofuranosyl-16α-hydroxyolean-12-ene-23α, 28β-dioic acid (1) and 3-O-α-L-arabinofuranosyl-(1 → 3)-β-D-glucopyranosyl 16α-hydroxyolean-12-ene-23α-oic acid, 28-O-β-D-glucopyranosyl-(1 → 6)-β-D-glycosyl ester (2) by chemical and extensive spectroscopic methods including IR, 1D, 2D NMR and HRESIMS. Both of the saponins were evaluated for their cytotoxicities against HEK-293, A-549 and HeLa human cancer cells using the MTT method. All compounds showed no substantial cytotoxic activity against tested cell lines. However, dianosides M-N and the n-butanol fraction exhibited considerable haemolysis in human erythrocyte cells. The immunomodulatory properties of dianosides M-N were also evaluated in activated whole blood cells by PMA plus ionomycin. Dianosides M-N increased IL-1β concentration significantly whereas the n-butanol fraction slightly augmented IL-1β secretion. All compounds did not change IL-2 and IFN-γ levels considerably.

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