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1 .     periforoside¢ñ
    ÏàËÆ¶È:59.4%
Chinese Pharmaceutical Journal          2011          46          823-826
Study on Chemical Constituents of Periploca forrestii Schlecht.
XU Ran,ZHANG Yuan-hu,ZHAO Yan-tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (16¦Á,20R,24S)-2,16,20,25-tetrahydroxy-24-methoxycucurbita-1,5-diene-3,11,22-trione 2-O-¦Â-D-glucopyranoside
37H56O13     ÏàËÆ¶È:59.4%
Journal of Natural Products          2011          74          2431-2437
Cucurbitane Glucosides from the Root of Machilus yaoshansis
Maoluo Gan, Mingtao Liu, Bo Liu, Sheng Lin, Yanling Zhang, Jiachen Zi, Weixia Song, Fei Ye, Xiaoguang Chen, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     2¦Á,19¦Á-dihydroxy-3-oxo-olean-12-en-oic acid 28-¦Â-D-glucopyranoside
C36H56O10     ÏàËÆ¶È:59.4%
Indian Journal of Chemistry Section B          2001          40B          354-356
New constituent from the roots of Terminalia arjuna: antifungal agent
B K Chouksey, S K Srivastava
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Isoarvenin III
C36H54O12     ÏàËÆ¶È:59.4%
Journal of Asian Natural Products Research          2012          14          528-532
Chemical constituents from the fruits of Trichosanthes kirilowii
Xue-Mei Fan, Gang Chen, Yi Sha, Xuan Lu, Ming-Xi Shen, Hong-Mei Ma & Yue-Hu Pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     sigmoiside F
C36H60O8     ÏàËÆ¶È:56.7%
Zeitschrift f¨¹r Naturforschung B          2008          63b          101-104
Sigmoiside F and Propyloxyamyrin, Two New Triterpenoid Derivatives from Erythrina sigmoidea (Fabaceae)
Jacques Kouam, Alain L. Meli, Muhammad I. Choudhary, and Zacharias T. Fomum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     9¦Â,25-cyclo 3¦Â-O-(¦Â-D-glucopyranosyl)echynocystic acid
C36H56O9     ÏàËÆ¶È:56.7%
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   Ì¼Æ×Ä£Äâͼ
7 .     cucurbitacin B
C30H42O6     ÏàËÆ¶È:56.7%
Shoyakugaku Zasshi          1993          47          334-337
Isolation and Identification of Cytotoxic Principles from Chrysosplenium japonicum MAXIM. (Saxifragaceae)
ARISAWA MUNEHISA, TAKESHIMA YUMIKO, BAI HUA, HAYASHI TOSHIMITSU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (20R,22R)-6¦Â,14¦Á-dihydroxy-2,3:20,22-bis(isopropylidenedioxy)-5¦Á-cholesta-7,25-diene
    ÏàËÆ¶È:55%
Russian Journal of Organic Chemistry          2005          41          1296-1305
Stereochemistry of Hydride Reduction of 20-Hydroxyecdysone Derivatives
V. N. Odinokov, R. G. Savchenko, R. V. Shafikov, S. R. Afon'kina and L. M. Khalilov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     24-hydroxyolean-12-en-3¦Â-yl-¦Â-D-glucopyranoside
C36H60O7     ÏàËÆ¶È:54.0%
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   Ì¼Æ×Ä£Äâͼ
10 .     (16¦Á,20R,24S)-16,24-epoxy-2,20,25-trihydroxycucurbita-1,5-diene-3,11,22-trione 2-O-¦Â-D-glucopyranoside
C36H52O12     ÏàËÆ¶È:54.0%
Journal of Natural Products          2011          74          2431-2437
Cucurbitane Glucosides from the Root of Machilus yaoshansis
Maoluo Gan, Mingtao Liu, Bo Liu, Sheng Lin, Yanling Zhang, Jiachen Zi, Weixia Song, Fei Ye, Xiaoguang Chen, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (16¦Á,20R,24R)-24N,25-carbamoyloxy-2,16,20-trihydroxycucurbita-1,5-diene-3,11,22-trione 2-O-¦Â-D-glucopyranoside
C37H53NO13     ÏàËÆ¶È:54.0%
Journal of Natural Products          2011          74          2431-2437
Cucurbitane Glucosides from the Root of Machilus yaoshansis
Maoluo Gan, Mingtao Liu, Bo Liu, Sheng Lin, Yanling Zhang, Jiachen Zi, Weixia Song, Fei Ye, Xiaoguang Chen, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (24R)-3¦Â,7¦Â,24,25,30-Pentahydroxy-1-ene-cycloartane24-O-¦Â-D-glucopyranoside
C36H60O10     ÏàËÆ¶È:54.0%
Natural Product Communications          2010          5          1557 - 1560
New Triterpene Glycosides from Camptosorus sibiricus
Ning Li*, Wan Xiao, Bailing Hou and Xian Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     2,22-dideoxyecdysone 25-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C39H64O14     ÏàËÆ¶È:53.8%
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   Ì¼Æ×Ä£Äâͼ
14 .     Machiluside B
    ÏàËÆ¶È:52.3%
Organic Letters          2011          Vol.13,No.11          2856-2859
Machilusides A and B: Structurally Unprecedented Homocucurbitane Glycosides from the Stem Bark of Machilus yaoshansis
Mingtao Liu, Maoluo Gan, Sheng Lin, Yanling Zhang, Jiachen Zi,Weixia Song,Xiaona Fan, Ying Liu, Yongchun Yang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     2¦Á, 19¦Á-dihydroxy-3-oxo-12-en-28-oic acid-28-oic acid-O-¦Á -L-rhamno-pyranosyl-(1¡ú4)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:52.3%
Indian Journal of Chemistry Section B          2004          43B          2731-2733
New biologically active constituents from Terminalia chebula stem bark
S K Srivastava* & S D Srivastava
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Sitosterol-3-O-¦Â-glucoside
    ÏàËÆ¶È:51.3%
Chemistry of Natural Compounds          2007          43          614-615
FLAVONOIDS FROM Trifolium resupinatum VAR. microcephalum
Emel Isik, Temine Sabudak, and Sevi Oksuz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     prosapogenin
C36H58O8     ÏàËÆ¶È:51.3%
Journal of Asian Natural Products Research          2001          3          213-217
Eclalbatin, a Triterpene Saponin from Eclipta Alba
R. K. UPADHYAY, M. B. PANDEY, R. N. JHA and V. B. PANDEY
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     momorcharaside B
C36H60O9     ÏàËÆ¶È:51.3%
Acta Pharmaceutica Sinica          1990          Vol 25          898-903
STUDIES ON THE ACTIVE CONSTITUENTS OF MOMORDICA CHARANTIA L.
ZJ Zhu; ZC Zhong; ZY Luo and ZY Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Brainesteroside D
C33H53O10     ÏàËÆ¶È:51.3%
Phytochemistry          2010          71          975-981
Phytoecdysteroids from the rhizomes of Brainea insignis
Ping Wu, Haihui Xie, Wenqin Tao, Shenyu Miao, Xiaoyi Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Mogroside I E1
C36H62O9     ÏàËÆ¶È:51.3%
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   Ì¼Æ×Ä£Äâͼ
21 .     È˲ÎÔíÜÕ Rh1
    ÏàËÆ¶È:51.3%
Journal of Shenyang Pharmaceutical University          1992          9          103-105
STUDIES ON THE ANTIARRHYTHMIC CONSTITUENTS FROM THE RHIZOMES OF PANAX GINSENG C.A.MEYER
Zhang Yonghe Lin Jingnan Pei Yuping Chen Yingjie Liu Chongming Xu Shuixu Yao Xinsheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     Cycloccidentaliside I
    ÏàËÆ¶È:51.3%
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   Ì¼Æ×Ä£Äâͼ
23 .     periplocin
    ÏàËÆ¶È:51.3%
Natural Product Research and Development          2006          18          772-774
Studies on Chemical Constituents of Periploca omeiensis
ZHANG Yuan-hu; CHEN Dong-lin; WANG Feng-peng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (3S,28S)3-O-acetyl-28-[3-azepan-prop-1-yn-1-yl]lup-20(29)-en-3,28-diol hydrochloride
C41H66NO3Cl     ÏàËÆ¶È:51.3%
Bioorganic & Medicinal Chemistry          2013          21          425-435
Cytotoxic betulin-derived hydroxypropargylamines trigger apoptosis
Ren¨¦ Csuk, Ronny Sczepek, Bianka Siewert, Christoph Nitsche
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     neomacroin
C32H48O6     ÏàËÆ¶È:51.3%
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   Ì¼Æ×Ä£Äâͼ
26 .     including periplocin
    ÏàËÆ¶È:51.3%
China Pharmacy          2010          21          4463-4465
Study on Chemical Constituents of Periploca calophylla
TAN Xiao-hong, ZHANG Yuan-hu, ZHOU Lan, TAN Ming-chun, SUN Qian-yun, HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     periplocin
    ÏàËÆ¶È:51.3%
China Pharmaceuticals          2009          18          24-26
Study on Chemical Constituents of Periploca Omeiensis
Wu Bin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     3¦Â-(¦Â-D-glucosyloxy)-16¦Á,23¦Á-epoxycucurbita-5,24-diene-11-one
    ÏàËÆ¶È:51.3%
Zeitschrift f¨¹r Naturforschung C          2000          55          141-145
A New Cucurbitacin Glycoside from Kageneckia oblonga (Rosaceae)
O. Munñoz, C. Delporte, N. Backhouse, S. Erazo, R. Negrete, S. Maldonado, J. L. L¨®pez-P¨¦rez, and A. S. Feliciano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     cauloside C
C41H66O13     ÏàËÆ¶È:51.2%
Journal of Agricultural and Food Chemistry          2001          49          5969-5974
Characterization of the Triterpene Saponins of the Roots and Rhizomes of Blue Cohosh (Caulophyllum Thalictroides)
Jin-Woo Jhoo, Shengmin Sang, Kan He, Xiaofang Cheng, Nanqun Zhu, Ruth E. Stark, Qun Yi Zheng, Robert T. Rosen, and Chi-Tang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     daphcalycinosidine C
C38H49NO12     ÏàËÆ¶È:50%
Journal of Natural Products          2004          67          1094-1099
New Alkaloids from Daphniphyllum calycinum
Hoda El Bitar, Van Hung Nguyen, Anthony Gramain, Thierry Svenet, and Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     picfeltarraenin IB
C42H64O14     ÏàËÆ¶È:50%
Journal of Natural Products          1998          61          757-761
Complement-Inhibiting Cucurbitacin Glycosides from Picria fel-terrae
Ying Huang, Tess De Bruyne, Sandra Apers, Yuliang Ma, Magda Claeys, Dirk Vanden Berghe, Luc Pieters, and Arnold Vlietinck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     Machiluside A
C42H62O17     ÏàËÆ¶È:50%
Organic Letters          2011          Vol.13,No.11          2856-2859
Machilusides A and B: Structurally Unprecedented Homocucurbitane Glycosides from the Stem Bark of Machilus yaoshansis
Mingtao Liu, Maoluo Gan, Sheng Lin, Yanling Zhang, Jiachen Zi,Weixia Song,Xiaona Fan, Ying Liu, Yongchun Yang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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