Haouamines A and B:  A New Class of Alkaloids from the Ascidian <i>Aplidium </i><i>h</i><i>aouarianum</i>

Leda Garrido, Marı́a J. Ortega, Javier Salvá

The Journal of Organic Chemistry · 2002 · 104 citations · 7 references

Concepts

Abstract

The chemical study of the ascidian Aplidium haouarianum has led to the isolation of the new metabolites haouamines A (1) and B (2) which belong to a novel class of alkaloids. The structure of 1 was established by interpretation of its spectroscopic data and those of the N-methyl derivative 3, and confirmed by X-ray crystallographic analysis. The structure of 2 was deduced by spectroscopic study of its peracetyl derivative 2a. In solution each haouamine exists as an unseparable mixture of two interconverting isomers derived by the presence of a highly strained 3-aza-[7]-paracyclophane moiety in their structures. Compound 1 exhibits a selective cytotoxic activity against the HT-29 human colon carcinoma cell line.

References

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