New Hydroquinone Monoterpenoid and Cembranoid-Related Metabolites from the Soft Coral Sarcophyton tenuispiculatum.
Tzu-Yin HuangChiung-Yao HuangShu-Rong ChenJing-Ru WengTzu-Hsuan TuYuan-Bin ChengShih-Hsiung WuJyh-Horng SheuPublished in: Marine drugs (2020)
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.
Keyphrases
- anti inflammatory
- transcription factor
- high throughput
- ms ms
- induced apoptosis
- inflammatory response
- dna binding
- insulin resistance
- cell cycle arrest
- molecular docking
- toll like receptor
- adipose tissue
- papillary thyroid
- squamous cell
- fatty acid
- type diabetes
- skeletal muscle
- squamous cell carcinoma
- oxidative stress
- metabolic syndrome
- lps induced
- immune response
- pi k akt
- young adults
- drug induced