| Literature DB >> 28981263 |
Alla A Kicha1, Anatoly I Kalinovsky1, Natalia V Ivanchina1, Timofey V Malyarenko1,2, Pavel S Dmitrenok1, Alexandra S Kuzmich1, Ekaterina V Sokolova1, Valentin A Stonik1,2.
Abstract
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.Entities:
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Year: 2017 PMID: 28981263 DOI: 10.1021/acs.jnatprod.7b00574
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050