Verproside
|
| 化合物名 | Verproside |
| 動物種 | ラット (Sprague-Dawley rat) |
| 代謝パラメータ |
Intravenous administration Intravenous administration Intravenous administration Intravenous administration Intravenous administration Intravenous administration |
| 代謝物 |
Verproside
|
| 関連生薬 | |
| 参考文献 | 1) Eun Jeong Park, Hyun Sook Lee, Sei-Ryang Oh, Hyeong-Kyu Lee, and Hye Suk Lee: Pharmacokinetics of verproside after intravenous and oral administration in rats. Arch. Pharm. Res. 32: 559-564 (2009). 2) Eun Jeong Park, Sei-Ryang Oh, Hyeong-Kyu Lee and Hye Suk Leea: Liquid chromatography–mass spectrometry for the simultaneous determination of the catalpol-related iridoid glucosides, verproside, isovanilloylcatalpol, catalposide and 6-O-veratroyl catalpol in rat plasma LC/MS analysis of the catalpol-related iridoid glucosides in rat plasma. Biomed. Chromatogr., 23: 980–986 (2009). |
| 論文備考 | ※Pharmacokinetic parameters of verproside after intravenous administration Values represent mean ± SD. * The values were significantly different from 2 and 5 mg/kg (p<0.05). Eun Jeong Park et al., Arch. Pharm. Res. 32: 559-564 (2009). ※Pharmacokinetic parameters of verproside after oral administration Values represent mean ± SD. * The values were significantly different from 2 and 5 mg/kg (p<0.05). Eun Jeong Park et al., Arch. Pharm. Res. 32: 559-564 (2009). |
