化學名稱 2,3,5,4\'-四羥基茋-2-o-β-d-葡萄糖苷
外觀 棕黃色
化學物質登錄號 82373-94-2
分子式
分子量 406.38
植物來源
異名
生物活性
鑑定
1HNMR
13CNMR
分析方法
儀器 矽膠G板
流動相 苯: 乙酸乙酯: 甲酸 =5: 5: 2
檢測器 UV λ365 nm
儀器 SHIMADAZU LC-10A HPLC
色譜柱 Spherigel C18 色譜柱, 5Lm, 4.6 x 150 mm, 30°C
流動相 乙腈: 水 = 17: 83, 1.0 mL/min
檢測器 UV λ320 nm
儀器 Shimadzu LC-2010C HT 系統及 Shimadzu HPLC 工作站 (Shimadzu, Japan)
色譜柱 Shimadzu VP-ODS 色譜柱 (150 mm × 4.6 mm I.D., 5 μm), 室溫
流動相 A: 甲醇, B: 水, 0-60 min 5-100% A
檢測器 UV λ254 nm
儀器 Waters Acquity™ Ultra Performance LC 系統 (Waters, USA)
色譜柱 ACQUITY UPLC BEH C18 色譜柱 (2.1 × 100 mm, 1.7 µm, UK), 40°C
流動相 A: 0.1% v/v甲酸水, B: 乙腈, 0-0.5 min 1% B, 0.5-10 min 1-20% B 10-12 min, 20-90% B 12-15 min 90-1% B, and 15-16 min 1% B, 0.5 mL/min
檢測器 Waters Xevo™ QTof MS (Waters), 一個四級杆及正交加速 TOF-MS (Waters), 包括一個 LockSpray™ 接口及一個ESI 源. 霧化器及輔助氣體: 氮氣, 碰撞氣體: 氬氣, 負離子模式, ESI 毛細管電壓: 2.5 kV, 源及反溶劑: 120 and 450°C, 脫溶劑及錐氣: 700 和30 L/h.採樣錐: 40 V, 提取錐: 4.0 V, lockspray 毛細管: 2.0 kV.碰撞能量: 30-45 eV.
樣品製備
方法一
5L 95% 乙醇提取樣品成濃縮漿, 超聲溶解於 300 ml 水並用等量乙醚和正丁醇分段三次。正丁醇上樣 D-101 大孔樹脂柱 (35 cm × 3.4 cm, 柱容積170 ml) 並用1700 ml 純水和 3400 ml 30% 乙醇洗脫。乙醇部分備用於分離。
TBE-300 高速逆流色譜 (Tauto Biotechnique, Shanghai, China) 及三個多層線圈分離柱 (管 I.D. = 1.5 mm, 總體積 = 300 ml) 及一個 20 ml 進樣環路及一個 S-1007 恒流泵 (Shenyitong Tech & Exploitation, Beijing, China), 一個 Model 8823B-UV 監視器 (Bingdayingchuang Sci & Tech, Beijing, China). 資料由 model N2000 色譜工作站 (Zhejiang University, Hangzhou, China) 收集
乙酸乙酯: 甲醇: 水 = 50: 1: 50, v/v/v, 流動相: 下相
2.0 mL/min, 800 rpm
Shimadzu LC-2010C HT 系統和 Shimadzu HPLC 工作站 (Shimadzu, Japan) 及 Shimadzu VP-ODS 色譜柱 (150 mm × 4.6 mm I.D., 5 μm) 室溫, A: 甲醇, B: 乙腈, 0-60 min 5-100% A, UV λ254 nm
參考文獻
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連結 中藥材圖像數據庫 藥用植物圖像數據庫 中藥標本數據庫

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