Cytotoxic Sesquiterpenoid Quinones and Quinols, and an 11-Membered Heterocycle, Kauamide, from the Hawaiian Marine Sponge Dactylospongia elegans

Abstract

Several known sesquiterpenoid quinones and quinols (1–9), and kauamide (10), a new polyketide-peptide containing an 11-membered heterocycle, were isolated from the extracts of the Hawaiian marine sponge Dactylospongia elegans. The planar structure of 10 was determined from spectroscopic analyses, and its relative and absolute configurations were established from density functional theory (DFT) calculations of the GIAO NMR shielding tensors, and advanced Marfey’s analysis of the N-MeLeu residue, respectively. Compounds 1 and 3 showed moderate inhibition of β-secretase 1 (BACE1), whereas 1–9 exhibited moderate to potent inhibition of growth of human glioma (U251) cells. Compounds 1–2 and 4–7 were also active against human pancreatic carcinoma (Panc-1) cells.

Document Details

Document Type
Pub Defense Publication
Publication Date
Jul 19, 2019
Source ID
10.3390/md17070423

Entities

People

  • Harper
  • Head
  • Neupane
  • Parrish
  • Turkson
  • Williams
  • Yip
  • Yoshida

Organizations

  • National Cancer Institute
  • National Institute on Aging
  • National Science Foundation
  • United States Department of Defense

Tags

Fields of Study

  • Chemistry

Readers

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