Isolation of Bioactive and Other Oxoaporphine Alkaloids from Two Annonaceous Plants, Xylopia aethiopica and Miliusa cf. banacea

George G. Harrigan, A. A. Leslie Gunatilaka, David G. I. Kingston, George W. Chan, Randall K. Johnson

Journal of Natural Products · 1994 · 87 citations · 0 references

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Abstract

The oxoaporphine alkaloids oxophoebine [1] and liriodenine [2] have been isolated from Xylopia aethiopica (Annonaceae). Both showed selective toxicity against DNA repair and recombination deficient mutants of the yeast Saccharomyces cerevisae. Three related but inactive compounds, oxoglaucine [3], O-methylmoschatoline [4], and lysicamine [5], were also isolated from this plant. Selective toxicity was also observed for 10-methoxyliriodenine (lauterine) [6] and 10-hydroxyliriodenine [7], two oxoaporphine alkaloids isolated from Miliusa cf. banacea (Annonaceae). The structure of 10-hydroxyliriodenine [7], a novel oxoaporphine, was determined by spectroscopic methods and chemical conversion to compound 6. The role of the bioactive oxoaporphine alkaloids as DNA topoisomerase inhibitors is discussed.