| Literature DB >> 31082231 |
Kyoung Jin Park1, Chung Sub Kim1, Zahra Khan2,3, Joonseok Oh4,5, Sun Yeou Kim2,3, Sang Un Choi6, Kang Ro Lee1.
Abstract
Seven new Securinega alkaloids, securingines A-G (1-7), together with seven known analogues (8-14), were isolated from the twigs of Securinega suffruticosa. Their chemical structures were elucidated by a combined approach of spectroscopic analysis, chemical methods, ECD calculations, and DP4+ probability analysis. The full NMR assignments and the absolute configuration of compound 8 are also reported. In addition, all the isolated phytochemicals (1-14) were assessed for their cytotoxic, anti-inflammatory, and potential neuroprotective activities. Compound 4 showed cytotoxic activity (IC50 values of 1.5-6.8 μM) against four human cell lines (A549, SK-OV-3, SK-MEL-2, and HCT15). Compounds 3, 10, 12, and 13 showed potent inhibitory effects on nitric oxide production (IC50 values of 12.6, 12.1, 1.1, and 7.7 μM, respectively) in lipopolysaccharide-stimulated murine microglia BV-2 cells. Compound 5 exhibited a nerve growth factor production effect (172.6 ± 1.2%) in C6 glioma cells at 20 μg/mL.Entities:
Year: 2019 PMID: 31082231 DOI: 10.1021/acs.jnatprod.9b00142
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050