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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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