天门冬科
立体化学
核磁共振波谱
细胞毒性T细胞
天然产物
化学
二维核磁共振波谱
生物
植物
生物化学
体外
作者
Tamam El‐Elimat,Reema Al‐Qiam,Joanna E. Burdette,Ahmed H. Al Sharie,Mohammad Al‐Gharaibeh,Nicholas H. Oberlies
出处
期刊:Phytochemistry
[Elsevier]
日期:2022-08-10
卷期号:203: 113343-113343
被引量:3
标识
DOI:10.1016/j.phytochem.2022.113343
摘要
Seven undescribed homoisoflavonoids were identified from the bulbs of Bellevalia longipes Post (Asparagaceae) as well as thirteen known and one natural homoisoflavonoid that had been reported as a synthetic product previously. A general approach for recognizing homoisoflavonoids via NMR spectroscopy data were presented. The undescribed compounds were: 8-dehydroxy-5-O-demethyl-6-hydroxyscillapersicone, 6-methoxyscillapersicone, 5-O-demethyl-6-methoxyscillapersicone, 8-O-methylscillapersicone, 4′-O-methylscillapersicone, 4′,8-O,O-dimethylscillapersicone, 3′-O-methylscillapersicone, and 3-hydroxy-desmethylophiopogonanone A. Structures were determined based on analysis of HRMS and NMR data, while absolute configurations were assigned using ECD spectroscopy. Human cancer cell lines were used to assess the cytotoxic activities of the isolated compounds, where 3-dehydroxy-3′-hydroxyeucomol showed IC50 values of 0.62 μM, 5.36 μM, and 2.52 μM, when tested against MDA-MB-435 (melanoma), MDA-MB-231 (breast), and OVCAR3 (ovarian) cells, respectively.
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