Planta Med 2018; 84(09/10): 729-735
DOI: 10.1055/a-0589-0525
Natural Product Chemistry and Analytical Studies
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Bioactive Segetane, Ingenane, and Jatrophane Diterpenes from Euphorbia taurinensis

Dóra Rédei
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
,
Norbert Kúsz
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
,
Gréta Sátori
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
,
Annamária Kincses
2   Department of Medical Microbiology and Immunobiology, University of Szeged, Szeged, Hungary
,
Gabriella Spengler
2   Department of Medical Microbiology and Immunobiology, University of Szeged, Szeged, Hungary
,
Katalin Burián
2   Department of Medical Microbiology and Immunobiology, University of Szeged, Szeged, Hungary
,
Zoltán Barina
3   Department of Botany, Hungarian Natural History Museum, Budapest, Hungary
,
Judit Hohmann
1   Department of Pharmacognosy, University of Szeged, Szeged, Hungary
4   Interdisciplinary Centre of Natural Products, University of Szeged, Szeged, Hungary
› Author Affiliations
Further Information

Publication History

received 12 January 2018
revised 02 March 2018

accepted 06 March 2018

Publication Date:
19 March 2018 (online)

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Abstract

A novel segetane (1) and jatrophane diterpene (2), together with five known diterpenoids possessing segetane (3), jatrophane (4), and ingenane skeletons (5 – 7), were isolated from the methanol extract of Euphorbia taurinensis All. The structure elucidation of the compounds was performed by means of extensive spectroscopic analysis, including HRESIMS and 1D (1H, J-modulated spin-echo carbon experiment) and 2D (HSQC, HMBC, COSY, NOESY) NMR experiments. The multidrug resistance reversing and cytotoxic effects of five diterpenes (1, 4 – 7) were studied on the L5178 mouse lymphoma cell line using rhodamine 123 accumulation and the MTT cell viability assay. Segetane and jatrophane diterpenes had no cytotoxic activity on the sensitive parent and multidrug resistance cells, while ingenane diterpenes showed a cytotoxic effect on both cell lines. Ingenanes 6 and 7 and segetane 1 demonstrated the remarkable multidrug resistance modulating effect at 20 µM.

Supporting Information