Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5218229 | Tetrahedron | 2013 | 7 Pages |
Abstract
Six new limonoids, Walsogynes B (1)-G (6), were isolated from the barks of Walsura chrysogyne, and their structures were determined on the basis of NMR and MS spectroscopic analyses in combination with NMR chemical shifts calculations. Walsogynes (1)-E (4) were concluded to be 11,12-seco limonoids sharing a unique dodecahydronaphtho[1,8-bc:5,4-bâ²câ²]difuran skeleton, and walsogynes F (5) and G (6) to be 11,12-seco limonoids with a dodecahydro-1H-naphtho[1,8-bc:3,4-câ²]difuran skeleton. Their absolute configurations were assigned through comparison of the calculated and experimental CD spectra. Walsogynes showed a moderate in vitro cytotoxic activity against various cancer cell lines.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alfarius E. Nugroho, Maho Okuda, Yukari Yamamoto, Yusuke Hirasawa, Chin-Piow Wong, Toshio Kaneda, Osamu Shirota, A.Hamid A. Hadi, Hiroshi Morita,