Cinerols, Nitrogenous Meroterpenoids from the Marine Sponge Dysidea cinerea.
Hou-Wen LinJing LiDan WangMeng-Meng ZhangLi-Yun LiuFan SunJing-Ya LiRobert J CaponHou-Wen LinPublished in: Journal of natural products (2019)
Eleven new nitrogenous meroterpenoids, cinerols A-K (1-11), were isolated from the marine sponge Dysidea cinerea collected in the South China Sea, and their structures were determined by detailed spectroscopic analysis. Cinerols A (1) and B (2) feature a rare 5H-pyrrolo[1,2a]benzimidazole moiety, while cinerols C-G (3-7) are examples of rare meroterpene benzoxazoles. The cinerols are noncytotoxic to human melanoma A375 cells at the concentration of 32 μM; however, selected cinerols exhibit moderate inhibitory activity against one or more of protein-tyrosine phosphatase 1B, ATP-citrate lyase, and SH2 domain-containing phosphatase-1 with IC50 values of 2.8-27 μM.
Keyphrases
- molecular docking
- induced apoptosis
- endothelial cells
- cell cycle arrest
- protein kinase
- machine learning
- induced pluripotent stem cells
- high intensity
- high resolution
- pluripotent stem cells
- binding protein
- protein protein
- signaling pathway
- molecular dynamics simulations
- small molecule
- amino acid
- oxidative stress
- mass spectrometry
- cell proliferation