中醫藥瀏覽 TCM Profile
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藥材   Compound  
植物豨薟 (1(10)E,4beta)-8beta-(Angeloyloxy)-6alpha,14,15-trihydroxygermacra-1(10),11(13)-dien-12-oic acid 12,6-lactone
(1(10)E,4E,8Z)-8-(angeloyoxy)-6alpha,15-dinhydroxy-14-oxogermacra-1(10),4,8,11(13)-tetraen-12-oic acid 12,6-lact
(1(10)E,4Z)-8beta-(Angeloyloxy)-9alpha,13-diethoxy-6alpha,15-dihydroxy-14-oxogermacra-1(10),4-dien-12-oic acid 1
(1(10)E,4Z)-8beta-(Angeloyloxy)-9alpha-ethoxy-6alpha,15-dihydroxy-13-methoxy-14-oxogermacra-1(10),4-dien-12-oic
(1(10)E,4Z)-8beta-(Angeloyloxy)-9alpha-ethoxy-6alpha,15-dihydroxy-14-oxogermacra-1(10),4,11(13)-trien-12-oic aci
(4beta,10E)-6alpha,14,15-trihydroxy-8beta-(isobutyryloxy)germacra-10,11(13)-diene-12-oic acid 12,6-lactone
11,12,13-Trinorguai-6-ene-4beta,10beta-diol
15,16-di-O-Acetyldarutoside
16-acetylkirenol
16-O-Acetyldarutigenol
16-O-Acetyldarutoside
2-methylbut-2-enoic acid (3aS,4S,5S,6Z,10Z,11aR)-5-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-bis(hydroxymeth
4beta,6alpha,15-Trihydroxy-8beta-(isobutyryloxy)-14-oxoguaia-9,11(13)-dien-12-oic acid 12,6-lactone
7beta-Hydroxydarutigenol
8beta-(Angeloyloxy)-4beta,6alpha,15-trihydroxyl-14-oxoguaia-9,11(13)-dien-12-oic acid 12,6-lactone
9beta-Hydroxydarutigenol
beta-D-glucopyranosyl-ent-2-oxo-15,16-dihydroxypimar-8(14)-en-19-oiclate
Darutigenol
Darutoside
ent-(15R),16,19-Trihydroxypimar-8(14)-ene 19-O-beta-D-glucopyranoside
ent-12alpha,16-epoxy-2beta,15alpha,19-trihydroxypimar-8(14)-ene
ent-12alpha,16-Epoxy-2beta,15alpha,19-trihydroxypimar-8-ene
ent-14beta,16-Epoxy-8-pimarene-2alpha,15alpha,19-triol
ent-14beta,16-epoxy-8-pimarene-3beta,15alpha-diol
ent-15-oxo-2beta,16,19-trihydroxypimar-8(14)-ene
ent-16-acetoxy-15-hydroxypimar-8(14)-en-3alpha-O-beta -glucopyranoside
ent-2-oxo-15,16,19-Trihydroxypimar-8(14)-en-19-O-beta-D-glucopyranoside
ent-2-oxo-15,16,19-trihydroxypimar-8(14)-ene
ent-2-oxo-15,16-dihydroxypimar-8(14)-en-16-O-beta-glucopyranoside
ent-2-oxo-3beta,15,16-trihydroxypimar-8(14)-en-3-O-beta-glucopyranoside
ent-2alpha,15,16,19-tetrahydroxypimar-8(14)-ene
ent-2beta,15,16,19-Tetrahydroxy-pimar-8(14)-en-19-O-beta-glucopyranoside
ent-2beta,15,16,19-tetrahydroxypimar-8(14)-en-19-O-beta-glucopyranoside
ent-3alpha,7beta,15,16-Tetrahydroxypimar-8(14)-ene
Hythiemoside B
Isopropylidenkirenol
Kirenol
lecocarpinolide
Pubeside A
pubeside B
pubeside C
Pubetallin
[1(10)-E,4Z]-8beta-Angeloyloxy-9alpha-methoxy-6alpha,15-dihydroxy-14-oxogermacra-1(10),4,11(13)-trien-12-oicacid
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參考文獻
[1] Giang, P. M., Son, P. T., Otsuka, H., ent-pimarane-type diterpenoids from Siegesbeckia orientalis L. Chem Pharm Bull (Tokyo) 2005, 53, 232-234.
[2] Sun, H. X., Wang, H., Immunosuppressive activity of the ethanol extract of Siegesbeckia orientalis on the immune responses to ovalbumin in mice. Chem Biodivers 2006, 3, 754-761.
[3] Wang, F., Cheng, X. L., Li, Y. J., Shi, S., Liu, J. K., ent-Pimarane diterpenoids from Siegesbeckia orientalis and structure revision of a related compound. J Nat Prod 2009, 72, 2005-2008.
[4] Wang, L. L., Hu, L. H., Chemical Constituents of Siegesbeckia orientalis L. Journal of Integrative Plant Biology 2006, 48, 991-995.
[5] Xiang, Y., Fan, C. Q., Yue, J. M., Novel Sesquiterpenoids from Siegesbeckia orientalis. HELVETICA CHIMICA ACTA 2005, 88, 160-170.
[6] Xiang, Y., Zhang, H., Fan, C. Q., Yue, J. M., Novel diterpenoids and diterpenoid glycosides from Siegesbeckia orientalis. J Nat Prod 2004, 67, 1517-1521.
腺梗豨薟 (-)-16,17-Dihydroxy-16β-kauran-19-oic acid
(-)-17-Hydroxy-16β-kauran-19-oic acid
12-Hydroxykirenol
16-O-Acetyldarutoside
16alpha,17-acetonide of ent-16alpha,17-dihydroxykauran-19-oic acid
16alpha,17-acetonide of ent-19-methyl-16alpha,17-dihydroxykauran-19-oic acid
16beta,17-dihydroxykauran-18-oic,acid
17-hydroxy-16alpha-ent-kauran-19-oic,acid
2-Keto-16-acetyl-kirenol
3,3’-Bis(6-methoxychroman)
7beta-Hydroxydarutigenol
Darutigenol
Darutoside
Daucosterol
ent-16-acetoxy-15-hydroxypimar-8(14)-en-3alpha-O-beta -glucopyranoside
ent-16-Acetoxy-3alpha,15-dihydroxy-14alpha-hydroperoxypimar-7-en-3alpha-O-beta-glucopyranoside
ent-16alpha,17,18-trihydroxykauran-19-oic acid
ent-16alpha,17-dihydroxykauran-19-oic acid
ent-16alphaH-kauran-17,19-dioic acid
ent-17,18-dihydroxy-16beta H-kauran-19-oicacid
ent-17-hydroxy-16alphaH-kauran-19-oic acid
ent-17-isobutyryloxy-18-hydroxykauran-19-oic acid
ent-18-Acetoxy-16alpha,17-dihydroxykauran-19-oic acid
ent-18-Acetoxy-16alpha-hydroxy-17-isobutyryloxykauran-19-oic acid
ent-18-Acetoxy-17-hydroxy-16betaH-kauran-19-oic acid
ent-18-Acetoxy-17-isobutyryloxy-16betaH-kauran-19-oic acid
ent-19-methyl-17-hydroxy-16alphaH-kauran-19-oic acid
ent-2-oxo-15,16,19-trihydroxypimar-8(14)-ene
ent-2beta,15,16-Trihydroxypimar-8(14)-en-19-oic acid
ent-3alpha,15,16,19-tetrahydroxypimar-8(14)-ene
ent-3alpha,15,16-Trihydroxypimar-8(14)-en-15,16-acetonide
ent-3alpha,15,16-Trihydroxypimar-8(14)-en-3alpha-O-beta-glucopyranoside-15,16-acetonide
ent-3alpha,7beta,15,16-Tetrahydroxypimar-8(14)-ene
Kirenol
Pubeside A
pubeside B
pubeside C
Pubeside D
Pubeside E
Siegesmethyletheric acid
wulingzhic,acid,a
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參考文獻
[1] Wang, R., Chen, W. H., Shi, Y. P., ent-kaurane and ent-pimarane diterpenoids from Siegesbeckia pubescens. J Nat Prod 2010, 73, 17-21.
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毛梗豨薟 No relevant compound uploaded TOP
參考文獻
[1] Kim, J. Y., Lim, H. J., Ryu, J. H., In vitro anti-inflammatory activity of 3-O-methyl-flavones isolated from Siegesbeckia glabrescens. Bioorg Med Chem Lett 2008, 18, 1511-1514.
腺梗豨薟 beta-Sitosterol
Daucosterol
Siegesmethyletheric acid
TOP
參考文獻
[1] Jian Yin, Ligong Guo, Modern Study of Chinese Drugs, Clinical Applications(7), Xueyuan Press, Beijing, 1993 (in Chinese).
[2] Yubin Ji (Chief Editor), Pharmacological Action, Application of Available Composition of Traditional Chinese Medicine, Heilongjiang Science and Technology Press, Heiiongjiang, 1995 (in Chinese).
[3] Dean Guo, Zhenggao Zhang, Guoqing Ye, Zhicen Lou, APS, 1997, 32(4), 282-285.
[4] Yun Ling, Yalin Zhang, Shaoqing Cai, Junhua Zheng, Zhongguo Yaowu Huaxue Zazhi, 1998, 8(1),46-47.
[5] Xiaojie Tong, Jinyun Zhou, Qicheng Fang, ZYZ, 1993, 28(3), 133-135.
[6] Jinping Liu, Guangxuan Wu, Yongmao Zhang, ZYZ, 1993, 28(5), 277-279.
[7] Heng Zhao, Baozhen Wang, Bingru Ma, Jinyan Sun, ZYZ, 1994, 29(9), 523-524.
[8] Liping Zhang, Changqi Hu, ZYZ, 1994, 29(10), 600-601.
[9] Mingyu Gui, Honggui Zhang, Yongri Jin, Guangxuan Wu, Wanru Peng, ZYZ, 1997, 32(4), 204-206.
[10] Yinjuan Bai, Yu Li, Yanping Shi, Youhua Hu, ZYZ, 1997, 32(8), 462-465.
[11] Yansheng Zhou, Muyun Ni, CCMM, 1994, 19(3), 162-163.
[12] Enjuan Zhang, Qinshu Kang, Zhao Zhang, CCMM, 1993, 18(1), 37-38.
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[17] Lei Tian, Lizhen Xu, Shilin Yang, CCMM, 1997, 22(12), 743-745.
[18] Peiyu Liang, Qi Zhou, Faxing Zhou, CCMM, 1998, 23(1), 39-40.
[19] Liping Xu, Jiansheng Liu, et al., CCMM, 1998, 23(9), 552-553.
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[23] Hongzheng Fu, Zhicen Lou, Xiuwei Yang, CTHC, 1997, 28(5),259-262.