4.8 Article

Biomimetic Synthesis and Biological Evaluation of Aplidiopsamine A

Journal

ORGANIC LETTERS
Volume 14, Issue 22, Pages 5808-5810

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol3024665

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Funding

  1. NIH [S10 RR019022]
  2. Department of Pharmacology
  3. William K. Warren, Jr. Funding

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The first total synthesis of Aplidiopsamine A, a rare 3H-pyrrolo[2,3-c]quinoline alkaloid from the Aplidiopsis confluata, has been achieved following the proposed biosynthesis. This biomimetic synthesis requires only five steps and proceeds in 20.8% overall yield. Biological evaluation across large panels of discrete molecular targets identified that Aplidiopsamine A is a highly selective PDE4 inhibitor, a target for numerous CNS disorders.

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