Abstract |
The structurally unique polyketide mumbaistatin is the strongest naturally occurring inhibitor of glucose-6-phosphate translocase-1 (G6P-T1), which is a promising target for drugs against type-2 diabetes mellitus and angiogenic processes associated with brain tumor development. Despite its high relevance, mumbaistatin has so far withstood all attempts towards its total synthesis. In the present study an efficient total synthesis of a deoxy- mumbaistatin analogue containing the complete carbon skeleton and a spirolactone motif closely resembling the natural product in its cyclized form was elaborated. Key steps of the synthesis are a Diels-Alder cycloaddition for the construction of the fully functionalized anthraquinone moiety and an anionic homo-Fries rearrangement to build up the tetra-ortho-substituted benzophenone core motif, from which a spiroketal lactone forms in a spontaneous process. The elaborated strategy opens an entry to a variety of new analogs of mumbaistatin and cyclo- mumbaistatin and may be exploited for the total synthesis of the natural product itself in the future.
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Authors | Stefan Neufeind, Nils Hülsken, Jörg-Martin Neudörfl, Nils Schlörer, Hans-Günther Schmalz |
Journal | Chemistry (Weinheim an der Bergstrasse, Germany)
(Chemistry)
Vol. 17
Issue 9
Pg. 2633-41
(Feb 25 2011)
ISSN: 1521-3765 [Electronic] Germany |
PMID | 21274958
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Chemical References |
- Anthraquinones
- Antiporters
- Biological Products
- Furans
- Monosaccharide Transport Proteins
- SLC37A4 protein, human
- Spiro Compounds
- mumbaistatin
- spiroketal
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Topics |
- Anthraquinones
(chemical synthesis, chemistry, pharmacology)
- Antiporters
(antagonists & inhibitors)
- Biological Products
(chemical synthesis, chemistry, pharmacology)
- Cyclization
- Furans
(chemical synthesis, chemistry)
- Models, Molecular
- Molecular Structure
- Monosaccharide Transport Proteins
(antagonists & inhibitors)
- Spiro Compounds
(chemical synthesis, chemistry)
- Stereoisomerism
- Structure-Activity Relationship
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