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  Chemistry and Biology of Roseophilin and the Prodigiosin Alkaloids: A Survey of the Last 2500 Years

Fürstner, A. (2003). Chemistry and Biology of Roseophilin and the Prodigiosin Alkaloids: A Survey of the Last 2500 Years. Angewandte Chemie, International Edition, 42(31), 3582-3603. doi:10.1002/anie.200300582.

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 Creators:
Fürstner, A.1, Author           
Affiliations:
1Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445584              

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Free keywords: alkaloids, heterocycles, immunosuppression, natural products, total synthesis
 Abstract: The pyrrole alkaloids of the prodigiosin family make up an unusual chapter in the chemistry of natural products. Owing to the characteristic red color of these secondary metabolites, colonies of the Gram-negative-producing bacteria may strikingly resemble droplets of blood. This phenomenon caused considerable confusion in the past and was likely responsible for many seemingly miraculous (prodigious) events. After the eventual transition from superstition to science, the prodigiosins started to attract considerable attention because of their promising physiological properties. Most interesting are the immunosuppressive activities at doses that are not cytotoxic, in particular since in vivo studies suggest that the prodigiosins act synergistically with cyclosporine A or FK 506, which are presently the dominant drugs in clinical immunosuppressive regimens. Furthermore, the chemistry of the closely related and structurally rather unique alkaloid roseophilin is summarized, a cytotoxic agent that recently became the focal point of many innovative total syntheses.

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Language(s): eng - English
 Dates: 2003-02-102003-08-072003-08-11
 Publication Status: Issued
 Pages: 22
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.200300582
 Degree: -

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Title: Angewandte Chemie, International Edition
  Other : Angew. Chem., Int. Ed.
  Other : Angew. Chem. Int. Ed
  Other : Angewandte Chemie International Edition
  Abbreviation : Angew. Chem. Int. Ed
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH Verlag GmbH & Co. KGaA
Pages: 22 Volume / Issue: 42 (31) Sequence Number: - Start / End Page: 3582 - 3603 Identifier: CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851