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藥材   Compound  
吳茱萸 1-methyl-2-((4Z,7Z)-trideca-4,7-dienyl)quinolin-4(1H)-one
1-Methyl-2-nonyl-4(1H)-quinolone
1-methyl-2-nonyl-4(1H)-quinolone
1-Methyl-2-pentadecyl-4(1H)-quinolone
1-methyl-2-tridecylquinolin-4(1H)-one
1-Methyl-2-undecyl-4(1H)-quinolone
1-Methyl-2-[(6z,9z)-6,9-pentadeca-dienyl]-4(1H)-quinolone
1-Methyl-2-[(Z)-10-pentadecenyl]-4-(1H)-quinolone
1-Methyl-2-[(Z)-6-pentadecenyl]-4(1H)-quinolone
2-nonyl-4(1H)-quinolone
2-undecyl-4(1H)-quinolone
3-Dimethylallyl-4-methoxy-2-quinolone
6alpha-Acetoxy-5-epilimonin
6beta-Acetoxy-5-epilimonin
Dihydroxyrutaecarpine
Evocarpine
Evodiamide
Evodiamine
Evodinone
Evodol
Goshuynic acid
Goshuyuamide-I
Goshuyuamide-II
Graucin A
N,N-Dimethyl-5-methoxy tryptamine
N-(2-Methulaminobenzoyl)tryfamine
N-Methylanthranylamide
Rutaecarpine
Rutaevine
Rutaevine acetate
Rutecarpine
Synepgrine
 TOP
參考文獻
[1] Iwata, H., Tezuka, Y., Kadota, S., Hiratsuka, A., Watabe, T., Mechanism-based inactivation of human liver microsomal CYP3A4 by rutaecarpine and limonin from Evodia fruit extract. Drug Metab Pharmacokinet 2005, 20, 34-45
[2] Jin, H. Z., Lee, J. H., Lee, D., Lee, H. S., et al., Quinolone alkaloids with inhibitory activity against nuclear factor of activated T cells from the fruits of Evodia rutaecarpa. Biol Pharm Bull 2004, 27, 926-928
[3] Lee, M. K., Hwang, B. Y., Lee, S. A., Oh, G. J., et al., 1-methyl-2-undecyl-4(1H)-quinolone as an irreversible and selective inhibitor of type B monoamine oxidase. Chem Pharm Bull (Tokyo) 2003, 51, 409-411
[4] Shin, Y. W., Bae, E. A., Cai, X. F., Lee, J. J., Kim, D. H., In vitro and in vivo antiallergic effect of the fructus of Evodia rutaecarpa and its constituents. Biol Pharm Bull 2007, 30, 197-199
[5] Ueng, Y. F., Don, M. J., Jan, W. C., Wang, S. Y., et al., Oxidative metabolism of the alkaloid rutaecarpine by human cytochrome P450. Drug Metab Dispos 2006, 34, 821-827.
[6] Jian Yin, Ligong Guo, Modern Study of Chinese Drugs, Clinical Applications(7), Xueyuan Press, Beijing, 1993 (in Chinese).
[7] Yubin Ji (Chief Editor), Pharmacological Action, Application of Available Composition of Traditional Chinese Medicine, Heilongjiang Science and Technology Press, Heiiongjiang, 1995 (in Chinese).
[8] Jiangsu New Medical College, Chinese Medicine Dictionary, Shanghai Science and Technology Press, Shanghai, 1979 (in Chinese).
[9] Yuanqing Tang, Xiaozhang Feng, Liang Huang, APS, 1996, 31(2), 151-155.
[10] Wenji Sun, Jinfang Sneng, Brief Handbook of Natural Active Compounds, Medicinal Science and Technology Press of China, Beijing, 1998 (in Chinese).
[11] Jiwu Wang, Qingxiang Xiao, Handbook of Effective Componentsin Vegetal Medicines, People's Health Press, Beijing, 1986 (in Chinese).
[12] Yunxiu Liu, Shurong Luo, NPRD, 2000, 12(1), 87-94.
[13] N. ShoJi, et al., JNP, 1988, 51(1), 161.
[14] T. Kamikado, et al., Agric. Bioi. Chem., 1978, 42(8), 1515.
石虎 No relevant compound uploaded TOP
參考文獻
疏毛吳茱萸 No relevant compound uploaded TOP
參考文獻
[1] Iwata, H., Tezuka, Y., Kadota, S., Hiratsuka, A., Watabe, T., Mechanism-based inactivation of human liver microsomal CYP3A4 by rutaecarpine and limonin from Evodia fruit extract. Drug Metab Pharmacokinet 2005, 20, 34-45
[2] Jin, H. Z., Lee, J. H., Lee, D., Lee, H. S., et al., Quinolone alkaloids with inhibitory activity against nuclear factor of activated T cells from the fruits of Evodia rutaecarpa. Biol Pharm Bull 2004, 27, 926-928
[3] Lee, M. K., Hwang, B. Y., Lee, S. A., Oh, G. J., et al., 1-methyl-2-undecyl-4(1H)-quinolone as an irreversible and selective inhibitor of type B monoamine oxidase. Chem Pharm Bull (Tokyo) 2003, 51, 409-411
[4] Shin, Y. W., Bae, E. A., Cai, X. F., Lee, J. J., Kim, D. H., In vitro and in vivo antiallergic effect of the fructus of Evodia rutaecarpa and its constituents. Biol Pharm Bull 2007, 30, 197-199
[5] Ueng, Y. F., Don, M. J., Jan, W. C., Wang, S. Y., et al., Oxidative metabolism of the alkaloid rutaecarpine by human cytochrome P450. Drug Metab Dispos 2006, 34, 821-827.