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1 . Mogroside I E1
C36H62O9 ÏàËÆ¶È:82.3%
Chinese Journal of Natural Medicines 2010 8 21-24
Chemical Constituents from the Stems and Leaves of Elaeocarpus glabripetalus
ZHANG Sheng; TAO Zheng-Ming; ZHANG Yi; SHEN Zheng-Wu; QIN Guo-Wei
Structure 13C NMR ̼Æ×Ä£Äâͼ
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2 . 24-¦Á-ethyl-20-ene-7-hydro-stigmast-8¦Â:14¦Â-di-3-O-¦Â-D-xylofuranoside
C34H58O6 ÏàËÆ¶È:58.8%
Asian Journal of Chemistry 1995 7 490-494
A New Steroidal Saponin from Trichosanthes dioica (Roxb.)
V.K. Saxena and R.K. Dave
Structure 13C NMR ̼Æ×Ä£Äâͼ
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3 . 3¦Â-O-5,25-stigmastadien¦Â-D-glucopyranoside
C35H58O6 ÏàËÆ¶È:58.8%
West China Journal of Pharmaceutical Sciences 2011 26 420-423
The separation and indentification of biflavonoids from Androsace umbellata
WANG Wen-jing, LEI Jun, XIAO Yun-chuan, XI Zhen, YU Min, HUANG Jing
Structure 13C NMR ̼Æ×Ä£Äâͼ
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4 . Snatzkein A
ÏàËÆ¶È:58.3%
Magnetic Resonance in Chemistry 1997 35 637-642
Structures of Two Novel Triterpene Saponins from Arenaira filicaulis Boiss.
M. Hani A. Elgamal, Hesham S. M. Soliman, Dalal T. Elmunajjed, G¨¢bor T¨®th, Andr¨¢s Simon and Helmut Duddeck
Structure 13C NMR ̼Æ×Ä£Äâͼ
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5 . 3¦Á,27-dihydroxy-cycloart-24E-en-26-oic acid
C30H48O ÏàËÆ¶È:57.5%
Phytochemistry 1989 28 1471-1477
Triterpenoids from Mangifera indica
V. Anjaneyulu,K. Ravi,K.Harischandra Prasad,J.D. Connolly
Structure 13C NMR ̼Æ×Ä£Äâͼ
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6 . neomacrotriol
C31H52O3 ÏàËÆ¶È:57.5%
Phytochemistry 2014 102 189-196
Cycloartane triterpenes from the leaves of Neoboutonia macrocalyx L. Original Research Article
Jane Namukobe, Bernard T. Kiremire, Robert Byamukama, John M. Kasenene, Vincent Dumontet, Françoise Gu¨¦ritte, Sabrina Krief, Isabelle Florent, John D. Kabasa
Structure 13C NMR ̼Æ×Ä£Äâͼ
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7 . uvariol
ÏàËÆ¶È:57.5%
Lishizhen Medicine and Materia Medica Research 2006 17 1178-1181
Chemical Constituents of Inonotus obliquus
ZHAO Fen-qin, PIAO Hui-shan
Structure 13C NMR ̼Æ×Ä£Äâͼ
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8 . cholesteryl-3-O-¦Â-D-glucoside
ÏàËÆ¶È:57.5%
Strait Pharmaceutical Journal 2012 24 50-53
Studies on Chemical Constituents of Livistona chinesis
CHEN Yan, YAO Hong, LI Shao-guang, HUANG Li-ying, LIN Xin-hua
Structure 13C NMR ̼Æ×Ä£Äâͼ
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9 . Cimicifugadine
C35H51NO8 ÏàËÆ¶È:57.1%
Organic Letters 2007 Vol. 9, No. 9 1813-1816
Cimicifugadine from Cimicifuga foetida,a New Class of Triterpene Alklaoids with Novel Reactivity
Chun Dan, Yan Zhou, Deng Ye,Shulin Peng, Lisheng Ding,Michael L. Gross, and Samuel X. Qiu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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10 . 24-hydroxyolean-12-en-3¦Â-yl-¦Â-D-glucopyranoside
C36H60O7 ÏàËÆ¶È:55.5%
Chemical & Pharmaceutical Bulletin 2010 58 1093-1095
Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities
Yu Cai and Tian-Ge Cai
Structure 13C NMR ̼Æ×Ä£Äâͼ
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11 . Cycloccidentaliside I
ÏàËÆ¶È:55.5%
Planta Medica 2012 78 821-827
Li, Shi-Fei; Di, Ying-Tong; Luo, Rong-Hua; Zheng, Yong-Tang; Wang, Yue-Hu; Fang, Xin; Zhang, Yu; Li, Ling; He, Hong-Ping; Li, Shun-Lin; Hao, Xiao-Jiang:
Cycloartane Triterpenoids from Cassia occidentalis
Structure 13C NMR ̼Æ×Ä£Äâͼ
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12 . 9¦Â,25-cyclo 3¦Â-O-(¦Â-D-glucopyranosyl)echynocystic acid
C36H56O9 ÏàËÆ¶È:55.5%
Journal of Ethnopharmacology 2011 135 78-87
Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities
Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat
Structure 13C NMR ̼Æ×Ä£Äâͼ
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13 . 2,22-dideoxy-20-hydroxyecdysone 25-O-¦Â-D-glucopyranoside
C33H54O10 ÏàËÆ¶È:54.5%
Phytochemistry 2009 70 430-436
Ecdysteroids and a sucrose phenylpropanoid ester from Froelichia floridana
Ping Wang, Shiyou Li, Stacy Ownby, Zhizhen Zhang, Wei Yuan, Wanli Zhang, R. Scott Beasley
Structure 13C NMR ̼Æ×Ä£Äâͼ
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14 . glyyunnansapogenin B2
ÏàËÆ¶È:54.5%
Acta Pharmaceutica Sinica 1995 30 27-33
NEW TRTEKPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS
JF Hu; ZL Ye and FJ Shen
Structure 13C NMR ̼Æ×Ä£Äâͼ
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15 . butyrospermol acetate
ÏàËÆ¶È:54.5%
China Journal of Chinese Materia Medica 2003 28 124-126
Studies on Chemical Constituents from the Bark of Morus macroura
WU Feng, SUN Shengguo, CHEN Ruoyun
Structure 13C NMR ̼Æ×Ä£Äâͼ
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16 . lup-20(30)-ene-3¦Á,29-diol
C30H50O2 ÏàËÆ¶È:54.5%
Phytochemistry 1999 50 839-841
A pentacyclic triterpene from Daphne oleoides
Nisar Ullah, Zaheer Ahmed, Saeed Ahmed, Pir Muhammad, Abdul Malik
Structure 13C NMR ̼Æ×Ä£Äâͼ
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17 . ocotillol
ÏàËÆ¶È:54.5%
Journal of Shenyang Pharmaceutical University 2008 25 35-38
Chemical constitunts from Sonneratia ovata
ZHENG Zhe, PEI Yue-hu
Structure 13C NMR ̼Æ×Ä£Äâͼ
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18 . penasterol
C30H48O3 ÏàËÆ¶È:54.5%
Journal of the Chemical Society, Perkin Transactions 1 1988 2403-2406
Penasterol, a novel antileukemic sterol from the okinawan marine sponge Penares sp.
Jie-fei Cheng, Jun'ichi Kobayashi, Hideshi Nakamura, Yasushi Ohizumi, Yoshimasa Hirata and Takuma Sasaki
Structure 13C NMR ̼Æ×Ä£Äâͼ
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19 . trametenolicacid
ÏàËÆ¶È:54.5%
Natural Product Research and Development 2010 22 433-436
Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus
ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin
Structure 13C NMR ̼Æ×Ä£Äâͼ
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20 . (20R,22R)-2¦Â,3¦Â:20,22-bis(isopropylidenedioxy)-5¦Â-cholest-8(14)-ene-6¦Â,25-diol
ÏàËÆ¶È:54.5%
Russian Journal of Organic Chemistry 2008 44 671-674
Analogs of ecdysteroids with a tetrasubstituted ¦¤8,14-bond
V. N. Odinokov, R. V. Shafikov, R. G. Savchenko, S. R. Afon¡¯kina and I. V. Galyautdinov, et al.
Structure 13C NMR ̼Æ×Ä£Äâͼ |
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