Four new briarane diterpenoids from Taiwanese Gorgonian Junceella fragilis

Chia Ching Liaw, Yu Chi Lin, Yun Sheng Lin, Chung Hsiung Chen, Tsong Long Hwang, Ya Ching Shen*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

20 Scopus citations

Abstract

Four new 8-hydroxybriarane diterpenoids, frajunolides P-S (1-4), together with umbraculolide A, juncenolide C, junceellonoid A and juncin R, were isolated from the acetone extract of the gorgonian Junceella fragilis, collected from the southeast coast of Taiwan. Compound 1 contains an unusual pivaloyloxy group at C-2, while 3 is a rare compound having a chlorine atom on the olefinic carbon (C-6). The structures of the isolated compounds were established by extensive spectroscopic analysis, including 1D- and 2D-NMR, as well as HRMS data. Compound 1 was further confirmed by X-ray crystallographic analysis. In the anti-inflammatory test, compounds 1 and 2 exhibited moderate inhibition on superoxide anion generation and elastase release by human neutrophils in response to formylmethionylleucyl-phenylalanine/dihydrocytochalasin B (fMLP/CB).

Original languageEnglish
Pages (from-to)2042-2053
Number of pages12
JournalMarine Drugs
Volume11
Issue number6
DOIs
StatePublished - 06 2013

Keywords

  • Anti-inflammatory
  • Briarane-type diterpenoids
  • Frajunolides
  • Junceella fragilis

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