簡介中醫藥瀏覽 TCM Profile
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| 藥材 | Compound | |
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1,1'-Bis(2,6-dihydroxy-3-acetyl-4-methoxyphenyl)methane 11-oxo-kansenonol 20-O-(2'E,4'E-Decadienoyl)ingenol 20-O-(2'E,4’Z-Decadienoyl)ingenol 20-o-(2,3-dimethylbutanoyl)-13-o-dodecanoylingenol 20-o-(decanoyl)-ingenol 20-O-(Decanoyl)ingenol 20-o-benzoyl-13-o-dodecanoateingenol 20-od-ingenol,e 20-od-ingenol,z 3-O-(2'E,4'E-Decadienoyl)-20-O-acetylingenol 3-O-(2'E,4'E-Decadienoyl)ingenol 3-O-(2'E,4'Z-Decadienoyl)-20-O-acetylingenol 3-O-(2'E,4'Z-Decadienoyl)-5-O-acetylingenol 3-O-(2'E,4'Z-Decadienoyl)ingenol 3-o-(2,3-dimethylbutanoyl)-13-o-decanoylingenol 3-O-(2,3-Dimethylbutanoyl)-13-O-dodecanoyl-20-acetylingenol 3-o-(2,3-dimethylbutanoyl)-13-o-dodecanoyl-20-deoxyingenol 3-o-(2,3-dimethylbutanoyl)-13-o-dodecanoyl-20-o-acetylingenol 3-o-(2,3-dimethylbutanoyl)-13-o-dodecanoylingenol 3-O-(2E,4E-Decadienoyl)-20-deoxyingenol 3-O-(2E,4Z-Decadienoyl)-20-deoxyingenol 3-o-benzoyl-13-o-dodecanoateingenol 3-o-benzoyl-20-deoxyingenol 5-O-(2'E,4'E-Decadienoyl)ingenol 5-o-benzoyl-20-deoxyingenol epi-kansenone Euphol Euphol Euphorbol Euphorbol kansenol kansenonol Kansuinin B kansuinine,a kansuinine,b kansuinine,c kansuinine,d kansuinine,e kansuinins,a kansuinins,d kansuinins,e kansuinins,f kansuinins,g kansuinins,h kansuiphorin,b kansuiphorin,c Methyl(2,4-dihydroxy-3-formyl-6-methoxy)phenylketone α-Euphol |
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| 參考文獻 [1] Miyata, S., Wang, L. Y., Yoshida, C., Kitanaka, S., Inhibition of cellular proliferation by diterpenes, topoisomerase II inhibitor. Bioorg Med Chem 2006, 14, 2048-2051. [2] Nunomura, S., Kitanaka, S., Ra, C., 3-O-(2,3-dimethylbutanoyl)-13-O-decanoylingenol from Euphorbia kansui suppresses IgE-mediated mast cell activation. Biol Pharm Bull 2006, 29, 286-290. [3] Okouchi, T., Abe, T., Araki, S., Arai, S., et al., Mechanism of proliferation arrest of embryonic cells of Xenopus by diterpene compounds. Bioorg Med Chem 2005, 13, 3847-3851. [4] Pan, Q., Ip, F. C., Ip, N. Y., Zhu, H. X., Min, Z. D., Activity of macrocyclic jatrophane diterpenes from Euphorbia kansui in a TrkA fibroblast survival assay. J Nat Prod 2004, 67, 1548-1551. [5] Shi, J. X., Li, Z. X., Nitoda, T., Izumi, M., et al., Three antinematodal diterpenes from Euphorbia kansui. Biosci Biotechnol Biochem 2007, 71, 1086-1089. [6] Shimokawa, K., Takamura, H., Uemura, D., Concise synthesis of a highly functionalized cyclopentane segment: toward the total synthesis of kansuinine A. Tetrahedron Letters 2007, 48, 5623-5625. [7] Wang, L. Y., Wang, N. L., Yao, X. S., Miyata, S., Kitanaka, S., Diterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus. J Nat Prod 2002, 65, 1246-1251. [8] Wang, L. Y., Wang, N. L., Yao, X. S., Miyata, S., Kitanaka, S., Diterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus (part 2). Chem Pharm Bull (Tokyo) 2003, 51, 935-941. [9] Wang, L. Y., Wang, N. L., Yao, X. S., Miyata, S., Kitanaka, S., Euphane and tirucallane triterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus. J Nat Prod 2003, 66, 630-633. [10] Wu, T. S., Lin, Y. M., Haruna, M., Pan, D. J., et al., Antitumor agents, 119. Kansuiphorins A and B, two novel antileukemic diterpene esters from Euphorbia kansui. J Nat Prod 1991, 54, 823-829. [11] Zhang, L., Shu, X., Ding, A., Yu, L., et al., LC�VDAD�VESI-MS�VMS Separation and Chemical Characterization of the Inflammatory Fraction of the Roots of Euphorbia kansui. CHROMATOGRAPHIA 2009, 70. [12] Jiangsu New Medical College, Chinese Medicine Dictionary, Shanghai Science and Technology Press, Shanghai, 1979 (in Chinese). [13] Chinese Materia Medica Editing Committee of the National Chinese Medicine and Pharmacology Bureau, Chinese Materia Medica (“ZHONG HUA BEN CAO”), Vol. 1 - Vol. 30, Shanghai Science and technology Press, Shanghai, 1999 (in Chinese). [14] D. Uemura, et al., Tetrahedron Lett, 1974, (29), 2527, 2529; 1975, (21), 1697, 1701. [15] Edited by Jiangsu New Medical College, Chinese Medicine Dictionary, Shanghai Science and technology Press, Shanghai, 1979 (in Chinese). [16] GB. Singh, et al., Planta Med, 1989, 55 (6), 498. [17] L-Y. WANG, et al., Chem Pharm Bull, 2003, 51 (8), 935. [18] LY. Wang, et al., JNP, 2002, 65 (9), 1246. [19] LY. Wang, et al., JNP, 2003, 66 (5), 630. [20] Q. Pan, et al., JNP, 2004, 67 (9), 1548. [21] Qin Pan, et al., CTHD, 2003, 34 (6), 489. [22] S. Oksuz, et al., Planta Med, 1993, 59 (5), 472. [23] T. Akihisa, et al., JNP, 2002, 65 (2), 158. [24] Wenji Sun, et al., Brief Handbook of Natural Active Compounds, Medicinal Science and Technology Press of China, Beijing, 1998 (in Chinese). [25] Wenxiang Wang, et al., APS, 1999, 34 (7), 514. [26] YL. Ding, et al., Phytochemistry, 1992, 31 (4), 1435. |
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