Exiguamine A, an Indoleamine-2,3-dioxygenase (IDO) Inhibitor Isolated from the Marine Sponge <i>Neopetrosia </i><i>exigua</i>

Harry C. Brastianos, Eduardo Vottero, Brian O. Patrick, Rob W. M. van Soest, Teatulohi Matainaho, A. Grant Mauk, Raymond J. Andersen

Journal of the American Chemical Society · 2006 · 125 citations · 4 references

Concepts

Abstract

Exiguamine A (1), a hexacyclic alkaloid with an unprecedented skeleton, has been isolated from the marine sponge Neopetrosia exigua collected in Papua New Guinea. The structure of exiguamine A (1) was elucidated by a combination of spectroscopic analysis and single-crystal X-ray diffraction analysis. Exiguamine A (1) has a Ki of 210 nM for inhibition of indoleamine-2,3-dioxygenase (IDO) in vitro, making it one of the most potent IDO inhibitors known to date. A putative biogenesis for the new exiguamine skeleton starts from DOPA, tryptophan, and N,N-dimethylhydantoin.

References

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