Furostane Series Asterosaponins and Other Unusual Steroid Oligoglycosides from the Tropical Starfish Pentaceraster regulus.
Alla A KichaAnatoly I KalinovskyNatalia V IvanchinaTimofey V MalyarenkoPavel S DmitrenokAlexandra S KuzmichEkaterina V SokolovaValentin A StonikPublished in: Journal of natural products (2017)
Seven new asterosaponins, pentaregulosides A-G (1-7), including two furostane-type steroid oligoglycosides (2, 3), along with four previously known compounds (8-11) were isolated from the ethanolic extract of the starfish Pentaceraster regulus, collected off the coast of Vietnam. The structures of 1-7 were elucidated by extensive NMR and ESIMS techniques as well as chemical transformations. The aglycons of compounds 1 and 3 have not previously been observed in starfish steroid oligoglycosides, while the aglycons of compounds 2 and 4-6 are very rare for this structural group. Compound 1 exhibited cytotoxic activity with an IC50 value of 6.4 ± 0.3 μM against RAW 264.7 murine macrophages. In contrast, nontoxic asterosaponins 3, 4, and 5 showed a potential immunomodulatory action at a concentration of 5 μM, reducing by 40%, 28%, and 55%, respectively, reactive oxygen species formation in the RAW 264.7 cells, co-stimulated with the pro-inflammatory endotoxic lipopolysaccharide from E. coli.
Keyphrases
- reactive oxygen species
- magnetic resonance
- induced apoptosis
- high resolution
- escherichia coli
- oxidative stress
- toll like receptor
- cell cycle arrest
- inflammatory response
- climate change
- magnetic resonance imaging
- lps induced
- immune response
- cell death
- anti inflammatory
- contrast enhanced
- mass spectrometry
- cell proliferation
- pi k akt