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.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Enzyme Inhibitors / chemistry*
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Enzyme Inhibitors / isolation & purification*
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Enzyme Inhibitors / metabolism
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Indoleamine-Pyrrole 2,3,-Dioxygenase / antagonists & inhibitors*
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Indoleamine-Pyrrole 2,3,-Dioxygenase / metabolism
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Indoles / chemistry*
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Indoles / isolation & purification*
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Magnetic Resonance Spectroscopy
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Models, Molecular
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Molecular Structure
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Oceans and Seas
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Porifera / chemistry*
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Porifera / metabolism
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Spiro Compounds / chemistry*
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Spiro Compounds / isolation & purification*
Substances
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Enzyme Inhibitors
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Indoleamine-Pyrrole 2,3,-Dioxygenase
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Indoles
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Spiro Compounds
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exiguamine A