Cytotoxicity and NMR Spectral Assigments of Ergolide and Bigelovin

Abstract
Two potent cytotoxic sesquiterpene lactones, ergolide (1) and bigelovin (2) were isolated from Inula hupehensis and I. helianthus-aquatica and their structures and NMR data were assigned unambiguously by using a combination of one- and two-dimensional NMR techniques and computer modeling calculations.

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