| Literature DB >> 33375440 |
Tzu-Yin Huang1, Chiung-Yao Huang2, Shu-Rong Chen3, Jing-Ru Weng1,2, Tzu-Hsuan Tu4, Yuan-Bin Cheng2, Shih-Hsiung Wu5, Jyh-Horng Sheu1,2,3,6.
Abstract
Chemical investigation of the marine soft coral Sarcophyton tenuispiculatum resulted in the isolation of a 1,4-dihydrobenzoquinone, sarcotenuhydroquinone (1), three new cembranoids, sarcotenusenes A‒C (2‒4), and ten previously reported metabolites 5-14. The chemical structures of all isolated metabolites were determined by detailed spectroscopic analyses. In biological assays, anti-inflammatory, cytotoxic, and peroxisome proliferator-activated receptor γ (PPAR-γ) transcription factor assays of all compounds were performed. None of the isolated compounds were found to exhibit activity in the PPAR-γ transcription factor assay. The anti-inflammatory assays showed that (+)-7α,8β-dihydroxydeepoxysarcophine (13) inhibited the production of IL-1β to 56 ± 1% at a concentration of 30 µM in lipopolysaccharide (LPS)-stimulated J774A.1 macrophage cells. In addition, 1 and 2 were found to exhibit cytotoxicity towards a panel of cancer cell lines.Entities:
Keywords: LPS-stimulated J774A.1 macrophage cells; PPAR-γ transcription factor; Sarcophyton tenuispiculatum; anti-inflammatory; cembranoid; cytotoxicity; hydroquinone
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Year: 2020 PMID: 33375440 PMCID: PMC7823492 DOI: 10.3390/md19010008
Source DB: PubMed Journal: Mar Drugs ISSN: 1660-3397 Impact factor: 5.118