Polyazamacrolides from ladybird beetles: Ring-size selective oligomerization

Frank C. Schroeder, Scott R. Smedley, Leah K. Gibbons, Jay J. Farmer, Athula B. Attygalle, Thomas Eisner, Jerrold Meinwald

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

The pupal defensive secretion of the 24-pointed ladybird beetle, Subcoccinella vigintiquatuorpunctata, consists of a mixture of macrocyclic polyamines, dominated by the three dimeric, 30-membered macrocycles 11-13, derived from the two building blocks 11-(2-hydoxyethylamino)-5-tetradecenoic acid (9) and 11-(2-hydoxyethylamino)-5,8-tetradecadienoic acid (10). Smaller amounts of the four possible cyclic trimers of 9 and 10 were also detected, corresponding to 45-membered macrocycles. Structural assignments were based on NMR-spectroscopic investigations and HPLC-MS analyses. In addition, the all-S absolute configuration of the S. vigintiquatuorpunctata macrocycles was determined by comparison of derivatives of the natural material with enantiomerically pure synthetic samples. Comparing this alkaloid mixture with that of the pupal defensive secretion in related ladybird beetle species indicates that the degree of oligomerization of the 2-hydroxyethylamino carboxylic acid building blocks can be carefully controlled by the insects.

Original languageEnglish
Pages (from-to)13387-13391
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume95
Issue number23
DOIs
StatePublished - 10 Nov 1998

Keywords

  • Alkaloids
  • Chemical defense
  • Combinatorial chemistry
  • Pupal secretion
  • Subcoccinella vigintiquatuorpunctata

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