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1 .     Hemslecin G
C32H50O9     ÏàËÆ¶È:84.3%
Acta Botanica Yunnanica          2003          25(5)          613-619
A New Cucurbitacin and A New Oleanolic Acid Glycosides from Hemsleya gigantha
CHEN Ya,QIU Ming-Hua, GU Kun, CHEN Jian-Chao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Hemslecin G
C32H50O9     ÏàËÆ¶È:84.3%
Chinese Chemical Letters          2003          14          475-478
Cucurbitacin and Triterpenoid Glycosides from Hemsleya giganthy
Ya CHEN2, Ming Hua CHIU1*, Kun GU2, Zhong Rong LI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     7-hydroxy-cucurbitacin F-25-O-acetate
C32H48O9     ÏàËÆ¶È:84.3%
Fitoterapia          2014          94          88-93
Cytotoxic cucurbitane triterpenoids isolated from the rhizomes of Hemsleya amabilis
Xu-Bing Chen, Guang-Yong Chen, Jun-Hua Liu, Min Lei, Yu-Hui Meng, De-An Guo, Xuan Liu, Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     cayaponoside A1
C37H54O13     ÏàËÆ¶È:70.9%
Chemical & Pharmaceutical Bulletin          1993          41          986-988
STRUCTURES OF NEW NON-AROMATIZED NOR-CUCURBITACIN GLUCOSIDES IN THE ROOTS OF CAYAPONIA TAYUYA
Eiji HIMENO,Tsuneatsu NAGAO,Junko HONDA,Hikaru OKABE,Nobuto IRINO and Tetsuo NAKASUMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     23,24-dihydrocucurbitacin F
    ÏàËÆ¶È:67.7%
Journal of Natural Products          2008          71(11)          1927-1929
Actin-Aggregating Cucurbitacins from Physocarpus capitatus
Katherine N. Maloney, Masaki Fujita, Ulrike S. Eggert, Frank C.Schroeder, Christine M. Field, Timothy J. Mitchison, and Jon Clardy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     schizandronic acid
    ÏàËÆ¶È:67.7%
China Journal of Chinese Materia Medica          2012          37          1597-1601
Chemical constituents of petroleum ether extract of fruits of Schisandra sphenanthera
LIU Haitao; LI Xingbo; ZHANG Jin; ZHU Yingxia; QI Yaodong; PENG Yong; ZHANG Bengang; XIAO Peigen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     colocynthol A
C32H44O9     ÏàËÆ¶È:65.6%
Chemical & Pharmaceutical Bulletin          2007          55(3)          428-434
Bioactive Saponins and Glycosides. XXVII.1) Structures of New Cucurbitane-Type Triterpene Glycosides and Antiallergic Constituents from Citrullus colocynthis
Masayuki YOSHIKAWA,Toshio MORIKAWA,Hisanori KOBAYASHI,Akihiko NAKAMURA,Koudai MATSUHIRA,Seikou NAKAMURA,and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     23,24-¶þÇâºùÂ«ËØB
C32H48O7     ÏàËÆ¶È:65.6%
China Journal of Chinese Materia Medica          2012          37          814-817
Chemical Components in Hemsleya chensnsis(¢ó)
DONG Jianyong; YUE Lei; SHAO Weiwei; XU Jinzhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     23,24-¶þÇâºùÂ«ËØF-25-ÒÒËáõ¥
C32H50O8     ÏàËÆ¶È:65.6%
China Journal of Chinese Materia Medica          2012          37          814-817
Chemical Components in Hemsleya chensnsis(¢ó)
DONG Jianyong; YUE Lei; SHAO Weiwei; XU Jinzhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     fevicordin B
    ÏàËÆ¶È:64.5%
Journal of Natural Products          1993          Vol 56          1506
Constituents of Fevillea cordifolia: New Norcucurbitacin and Cucurbitacin Glycosides
Hans Achenbach, Reiner Waibel, Ursula Hefter-B¨¹bl, Manuel A. Constenla
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     23,24-Dihydrocucurbitacin F
    ÏàËÆ¶È:64.5%
Zeitschrift f¨¹r Naturforschung B          2008          63b          1415-1420
Socotroside, a New Pentacyclic Cucurbitane Glycoside from Dendrosicyos socotrana
Osama B. Abdel Halim, El-Sayed M. Marawan, Ali A. El-Gamal, and Mona G. Zaghloul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     2¦Â,3¦Á,16¦Á,20(R),24(S),25-hexahydroxy-9-methyl-19-norlanost-5-en-11,22-dione
C30H48O8     ÏàËÆ¶È:64.5%
Fitoterapia          2014          94          88-93
Cytotoxic cucurbitane triterpenoids isolated from the rhizomes of Hemsleya amabilis
Xu-Bing Chen, Guang-Yong Chen, Jun-Hua Liu, Min Lei, Yu-Hui Meng, De-An Guo, Xuan Liu, Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Cucurbitacin U
    ÏàËÆ¶È:64.5%
Chinese Journal of Applied & Environmental Biology          2009          15          615-620
Chemical Constituents from Polygonum perfoliatum
LI Hongfang; MA Qingyun; LIU Yuqing; QIAN Jinfu; ZHOU Jun & ZHAO Youxing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     dihydrocucurbitacin B
    ÏàËÆ¶È:62.5%
Chemical & Pharmaceutical Bulletin          2004          52(3)          345-349
Cytotoxic and Anti-HIV Principles from the Rhizomes of Begonia nantoensis
Pei-Lin WU,Fu-Wen LIN,Tian-Shung WU,Chang-Sheng KUOH,Kuo-Hsiung LEE,and Shiow-Ju LEE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     6-acetoxy-20R,24S-epoxycycloartan-16¦Â,25-diol-3-one
    ÏàËÆ¶È:62.5%
Chemistry of Natural Compounds          2008          44          732-737
TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXVIII. CHEMICAL TRANSFORMATION OF CYCLOARTANES.VI. PARTIAL SYNTHESIS OF CYCLOADSURGENINa
I. M. Isaev, D. A. Iskenderov, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     23,24-dihydrocucurbitacin B
C34H52O9     ÏàËÆ¶È:62.5%
Natural Product Research          2003          17          229-233
Morierinin: A New Cytotoxic Cucurbitacin from the Leaves of Morierina Montana Vieill.
Marc Litaudon; Christianne Gaspard; Thierry S¨¦venet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     dihydroisocucurbitacin B-25-acetate
    ÏàËÆ¶È:62.5%
Chinese Traditional and Herbal Drugs          2012          43          432-435
Isolation and identification of chemical constituents from Citrullus colocynthis
MIAO Jing; ZHANG Jie; DENG Shi-ming; DAI Bin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     dihydrocucurbitacin E
    ÏàËÆ¶È:62.5%
Natural Product Research and Development          2014          26          354-357
Five Cucurbitacins from Aquilaria sinensis Peels and Their Cytotoxic Activities
ZHANG Xing, TAO Mei-hua, CHEN Yu-chan, GAO Xiao-xia, TAN Yu-zhi*, ZHANG Wei-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (22Z,24E)-3-oxocycloart-22,24-dien-26-oic acid
C30H44O3     ÏàËÆ¶È:61.2%
Journal of Natural Products          2009          72          1283-1287
Chemical Constituents of Propolis from Myanmar and Their Preferential Cytotoxicity against a Human Pancreatic Cancer Cell Line
Feng Li, Suresh Awale, Hongyan Zhang, Yasuhiro Tezuka, Hiroyasu Esumi, and Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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