化学名称 苦参查尔酮
外观 白色结晶
化学物质登录号 34981-25-4
分子式
分子量 438.51
植物来源
生物活性
鉴定 熔点 115°C
旋亮度 [α]17D+6.6 (c, 1 乙醇)
13CNMR
分析方法
仪器 Waters ACQUITY UPLC™ 系统 (Waters Corp., MA, USA)
色谱柱 Waters ACQUITY BEH C18 色谱柱 (100 × 2.1 mm, 1.7 μm, Waters Corp., Ireland)
流动相 A: 乙腈, B: 水, 0-5 min 40-100% A, 0.3 mL/min
检测器 ELSD, 漂移管: 75°C, 雾化气: 48°C, gain: 300°C, 气压: 45 psi
仪器 LC-NMR 系统 (Varian, Palo Alto, CA, USA)
色谱柱 YMC hydrosphere C18 反相色谱柱 (4.6 x 150 mm, 3µm)
流动相 A; 乙腈, B: D2O, 0-60min 45~65% A, 0.8 mL/min
检测器 UV λ320 nm, Varian 500 MHz 色谱仪包括 LC-NMR 低温探针, 60µL 流动槽. Varian WET 溶剂系统及 scout± scan, 自由感应衰减 (FID): 16 K 数据点, 质朴宽度 12000 Hz, 3µs 90° 脉冲, 2 s 收集时间和1 s 脉冲衰减.
仪器 Waters 1525 HPLC 仪
色谱柱 Phenomenex Luna C18 色谱柱 (250 mm × 4.6 mm, 5µm) column, 35°C
流动相 A: 乙腈, B: 水, 0-35min 45-69% A, 1mL/min
检测器 UV λ365 nm
样品制备
方法一
TBE-1000A HSCCC (Shanghai, Tauto Biotech, China) 包括三个聚四氟乙烯线圈 (总量, 1000 ml)
正己烷: 乙酸乙酯: 甲醇: 水 = 1: 1: 1: 1, v/v, 流动相: 下相
8.0 mL/min, 500 rpm
UV λ254 nm
参考文献
[1] Chan, B. C.-L., et al. (2012). "Quick identification of kuraridin, a noncytotoxic anti-MRSA (methicillin-resistant Staphylococcus aureus) agent from Sophora flavescens using high-speed counter-current chromatography." Journal of Chromatography B 880(0): 157-162.
[2] Jung, M. J., et al. (2004). "Isolation of flavonoids and a cerebroside from the stem bark of Albizzia julibrissin." Arch. Pharmacal Res. 27(6): 593-599.
[3] Quang, T. H., et al. (2013). "Anti-Inflammatory and PPAR Transactivational Properties of Flavonoids from the Roots of Sophora flavescens." Phytother. Res. 27(9): 1300-1307.
[4] Sohn, H. Y., et al. (2004). "Antimicrobial and cytotoxic activity of 18 prenylated flavonoids isolated from medicinal plants: Morus alba L., Morus mongolica Schneider, Broussnetia papyrifera (L.) Vent, Sophora flavescens Ait and Echinosophora koreensis Nakai." Phytomedicine 11(7-8): 666-672.
[5] Jeong, T.-S., et al. (2008). "Low density lipoprotein (LDL)-antioxidant flavonoids from roots of Sophora flavescens." Biol Pharm Bull 31(11): 2097-2102.
[6] Han, J.-M., et al. (2010). "Lavandulyl flavonoids from Sophora flavescens suppress lipopolysaccharide-induced activation of nuclear factor-κB and mitogen-activated protein kinases in RAW264.7 cells." Biol. Pharm. Bull. 33(6): 1019-1023.
[7] Chung, M. Y., et al. (2004). "In vitro inhibition of diacylglycerol acyltransferase by prenylflavonoids from Sophora flavescens." Planta Med. 70(3): 258-260.
[8] Kim, S. J., et al. (2003). "Tyrosinase inhibitory prenylated flavonoids from Sophora flavescens." Biol Pharm Bull 26(9): 1348-1350.
[9] Rasul, A., et al. (2011). "Induction of mitochondria-mediated apoptosis in human gastric adenocarcinoma SGC-7901 cells by kuraridin and Nor-kurarinone isolated from Sophora flavescens." Asian Pac J Cancer Prev 12(10): 2499-2504.
[10] Kim, S. J., et al. (2010). "Fast identification of flavonoids in the roots of Sophora flavescens by on-flow LC-NMR." J. Med. Plants Res. 4(23): 2452-2459.
[11] Xu, C., et al. (2008). "HPLC determination of contents of four flavonoids in different samples of Sophora flavescens in market." Zhongyao Xinyao Yu Linchuang Yaoli 19(3): 210-212.
连结 中药材图像数据库 药用植物图像数据库 中药标本数据库

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