Molecules (Dec 2018)

Scalalactams A–D, Scalarane Sesterterpenes with a γ-Lactam Moiety from a Korean <i>Spongia</i> Sp. Marine Sponge

  • Inho Yang,
  • Jusung Lee,
  • Jihye Lee,
  • Dongyup Hahn,
  • Jungwook Chin,
  • Dong Hwan Won,
  • Jaeyoung Ko,
  • Hyukjae Choi,
  • Ahreum Hong,
  • Sang-Jip Nam,
  • Heonjoong Kang

DOI
https://doi.org/10.3390/molecules23123187
Journal volume & issue
Vol. 23, no. 12
p. 3187

Abstract

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Intensive study on the chemical components of a Korean marine sponge, Spongia sp., has led to the isolation of four new scalarane sesterterpenes, scalalactams A⁻D (1⁻4). Their chemical structures were elucidated from the analysis of spectroscopic data including 1D-and 2D-NMR as well as MS data. Scalalactams A⁻D (1⁻4) possess a scalarane carbon skeleton with a rare structural feature of a γ-lactam moiety within the molecules. Scalalactams A and B (1 and 2) have an extended isopropanyl chain at the lactam ring, and scalalactams C and D (3 and 4) possess a phenethyl group at the lactam ring moiety. Scalalactams A⁻D (1⁻4) did not show FXR antagonistic activity nor cytotoxicity up to 100 μM.

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