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14.24,18.31,18.53,19.54,20.24,21.35,25.68,26.24,26.36,26.70,28.32,30.14,30.23,30.64,32.21,33.05,35.82,36.64,39.28,40.74,45.56,47.35,48.20,49.07,52.26,79.08,125.85,139.61


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9.01,14.30,14.35,18.00,19.03,20.56,22.18,22.24,22.80,22.92,25.01,25.88,27.41,27.45,27.47,29.29,29.38,29.45,29.59,29.65,29.76,29.82,29.88,29.92,30.00,31.76,32.16,33.50,34.27,34.62,34.64,37.99,40.34,41.77,41.81,55.21,62.40,68.70,73.71,74.33,79.06,128.12,128.38,129.87,129.94,130.17,130.32,130.48,152.00,172.39,172.44,174.45
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1 .     cycloart-23 Z-en-3¦Â,25-diol
    ÏàËÆ¶È:96.5%
Phytochemistry          1996          41          1163-1168
A 3, 4-seco-8¦ÂH-fernadienoic acid and other constituents from Euphorbia chamaesyce
Reiko Tanaka, Tomoko Ida, Shunji Kita, Wasuke Kamisako, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:96.5%
Chinese Traditional and Herbal Drugs          2000          31          409-412
Triterpenes from Butter-and-Eggs (Linaria vulgaris)
Shenyang Pharmaceutical University (Shenyang )Hua Huiming; Hou Bailing; Li Wen and Li Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (23Z)-9,19-cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:96.5%
Journal of Shenyang Pharmaceutical University          2003          20          252-254
Cycloartane triterpenoids from the pericarp of Sphaerophysa salsula DC.
LI Guo-yu, WANG Jin-hui, LI Ning, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (23Z)-9,19-cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:96.5%
Natural Product Research and Development          2006          18          411-414
Phytochemical Study on Zehneria maysorensis
LI Hong-juan;LUO Ying-gang; HE Zhi-heng; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Journal of Natural Products          2000          63          636-642
Phytochemical Investigation of Aglaia rubiginosa
S. Weber, J. Puripattanavong, V. Brecht, and A. W. Frahm
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     cycloart-23-ene-3¦Â,-25-diol
    ÏàËÆ¶È:93.3%
Journal of Natural Products          1996          59          343-347
Cycloartane Derivatives from Tillandsia usneoides
Gabriela M. Cabrera, Mariana Gallo, and Alicia M. Seldes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Planta Medica          1987          53          577
Further Triterpenes from the Stem Bark of Euphorbia tirucalli
Abdul Qasim Khan, Zaheer Ahmed, Najam-ul-Hussain Kazml,and Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     cycloart-23-ene-3, 25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Acta Botanica Yunnanica          1999          21(2)          260-264
The constituents of Ervatamia divaricata
YU Yang,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (23Z)-cycloart-23-en-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Chemical & Pharmaceutical Bulletin          1998          46          1408-1411
New Sterols and Triterpenoids of Ficus pumila Fruit
Junichi KITAJIMA,Kaoru KIMIZUKA and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     9,19-cycloergost-23-en-3,25-diol
    ÏàËÆ¶È:93.3%
China Journal of Chinese Materia Medica          2009          34          705-707
Study on chemical constituents from Cicuta virosa var. latisecta
L I Zhenlin1, Q I AN Shihui, PU Sheban
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     cycloart-22-ene-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
China Journal of Chinese Materia Medica          2008          33          405-408
Studies on phenolic compounds from Stellera chamaejasme
FENG Bao, GONG Xiaojie, SHI Liying, JIAN Ge, PEI Yue-hu, WANG Yong-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
China Journal of Chinese Materia Medica          2006          31          1166-1168
Studies on constituents from root and stem of Ervatamia hainanensis
HUANG Jianpeng, MA Yangmin, JIANG Jianshuang, ZHANG Peicheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     cycloart-23-en-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Records of Natural Products          2008          2          39-45
Chemical Investigation of Euphorbia schimperi C. Presl
Azza R. Abdel-Monem, Essam Abdel-Sattar, Fathalla M. Harraz, and Frank Petereit
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     cycloart-23Z-ene-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Phytochemistry          1994          35          1017-1022
Cycloartane triterpene from Juncus effusus
Marina Della Greca, Antonio Molinaro, Pietro Monaco and Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     Cycloart-23-ene-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Magnetic Resonance in Chemistry          2012          50          52-57
1H and 13C NMR characterization of new cycloartane triterpenes from Mangifera indica
Carolina Escobedo-Mart¨ªnez, M. Concepci¨®n Lozada,Sim¨®n Hern¨¢ndez-Ortega, Mar¨ªa Luisa Villarreal, Dino Gnecco,Ra¨²l G. Enr¨ªqueza and William Reynolds
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     cycloart-23Z-ene-3¦Â,25-dio l
C30H50O2     ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2010          41          1608-1612
Chemical constituents in Senecio vulgaris
LIU Yong-heng; ZHANG Zi-ping; WANG Yong-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Chinese Traditional and Herbal Drugs          2005          36          669-671
ÌÙ¿à²Î»¯Ñ§³É·ÖÑо¿(¢ò)
ÕÅÁÕ,ÐìÀöÕä,ÑîÊÀÁÖ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     23-cycloarten-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2005          3          31-33
Chemical Constituents of Euphorbia antiquorum
SANG Yi-Shu; SHI Hai-Ming; JIA Liang; LIU Xue-Ting; MIN Zhi-Da
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     cycloart-23-ene-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2008          6          271-274
Chemical Constituents from the Roots and Stems of Ervatamia hainanensis
JIN Li; LU Jia; JIN Yong-Sheng; YANG Xiang-Nan; CHEN Hai-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     sterculin A
    ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2009          7          425-427
Chemical Constituents from Houttuynia cordata
QU Wei; LIANG Jing-Yu; LI Meng-Ran
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     9,19-cyclolanost-23E-ene-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2010          8          183-185
Chemical Constituents from Euphorbia ebracteolata
DENG Bin; MU Shu-Zhen; HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     cycloart-23-en-3¦Â,25-diol)
    ÏàËÆ¶È:93.3%
Chinese Pharmaceutical Journal          2010          45          1535-1538
Studies on Chemical Constituents of Stamen Nelumbinis
CHEN Yan-yan, TANG Yu-ping, DUAN Jin-ao, GUO Sheng, WU Qi-cheng, SHANG Er-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     cycloart-23-ene-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Modern Chinese Medicine          2007          9(7)          13-14
Studies on the Constituents of Senecio laetus Edgew.
Jin Jun, Zhang Chaofeng, ZhangMian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     cycloart-23Z-en-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Natural Product Research and Development          2005          17          437-439
Lipid Constituents from Euphorbia humifusa Wild.
LIU Run-hui; KONG Ling-yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     23(Z)-cycloart-23-en-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Journal of the Chinese Chemical Society          2007          54          1565-1572
Triterpenoids and Other Constituents from Euphorbia humifusa
Ying-Ge Pei, Quan-Xiang Wu and Yan-Ping Shi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     23(Z)-cycloart-23-en-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2012          10          0299-0302
Chemical constituents of Euphorbia fischeriana
Xiao-Yang WANG, Li-Ping LIU, Ting-Guo KANG, Hong-Bing WANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     cycloart-22-en-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Chinese Journal of Natural Medicines          2012          10          0299-0302
Chemical constituents of Euphorbia fischeriana
Xiao-Yang WANG, Li-Ping LIU, Ting-Guo KANG, Hong-Bing WANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     9,19-Cyclolanost-23-ene-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:93.3%
Journal of the Brazilian Chemical Society          2002          13          276-280
Chemical Constituents from Bombacopsis glabra (Pasq.) A. Robyns: Complet 1H and 13C NMR Assignments and X Ray Structure of 5-Hydroxy-3,6,7,8,4'-pentamethoxyflavone
Vanderl¨²cia F. Paula, Luiz C. A. Barbosa, William Errington, Oliver W. Howarth and Mariluze P. Cruz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     cycloart-23-ene-3¦Â,25-diol
    ÏàËÆ¶È:93.3%
Chinese Pharmaceutical Journal          2012          47          953-955
Study on Chemical Components of Dendrobium officinale Protocorm
MENG Zhi-xia; SHU Ying; WANG Chun-lan; GUO Shun-xing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     griffith ine A
C30H50O2,     ÏàËÆ¶È:93.1%
Acta Botanica Yunnanica          1997          19(3)          321-323
STUDIES ON CHEMICAL CONSTITUENTS FROM LEAVES OF GONIOTHALAMU SGRIFFITH II
L i Chaom ing,L iu Zhenglian ,M u Q ing, Sun Handong,Zheng Hu ilan, Tao Guoda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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Çç·ïÒÇ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-19 16:46:16
1 .     5¦Á-stigmast-9(11)-en-3¦Â-ol-tetraco santrienoic acid ester
    ÏàËÆ¶È:69.2%
China Journal of Chinese Materia Medica          1996          21          666-667
Studies on Chemical Components of Cynomorium songaricum Rupr.
Xu Xiuzhi, Zhang Chengzhong and Li Chong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     Benzyl 3¦Á,7¦Á,12¦Á-tris(decanoyloxy)-5¦Â-cholate
C61H100O8     ÏàËÆ¶È:67.3%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Benzyl¦Á3¦Á-acetoxy-7¦Á,12¦Á-bis(hexadecanoyloxy)-5¦Â-cholate
C65H108O8     ÏàËÆ¶È:67.3%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     7¦Â-tert-Butyldimethylsilyloxysitosteryl oleate
C53H96O3Si     ÏàËÆ¶È:65.3%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     urs-12-en-3¦Â-O-9E,12E-octadecadienoate
C19H34O2     ÏàËÆ¶È:65.3%
Journal of Asian Natural Products Research          2009          11          583-587
A new lipid and other constituents from the rhizomes of Nelumbo nucifera
Prabir Kumar Chaudhuri and Deepika Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     3¦Â-stearyloxy-urs-12-ene
C48H84O2     ÏàËÆ¶È:65.3%
Magnetic Resonance in Chemistry          2006          44          127-131
Structural determination of 3¦Â-stearyloxy-urs-12-ene from Maytenus salicifolia by 1D and 2D NMR and quantitative 13C NMR spectroscopy (pages 127¨C131)
R. R. S. Miranda, G. D. F. Silva, L. P. Duarte, I. C. P. Fortes and S. A. Vieira Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     PX12
    ÏàËÆ¶È:65.3%
Journal of the Chemical Society, Perkin Transactions 1          1996                   2651-2656
Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces
Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Benzyl 3¦Á-benzyloxycarboxy-7¦Á,12¦Á-bis(decanoyloxy)-5¦Â-cholate
C59H88O9     ÏàËÆ¶È:65.3%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Benzyl¦Á3¦Á,7¦Á,12¦Á-tris(hexadecanoyloxy)-5¦Â-cholate
C79H136O8     ÏàËÆ¶È:65.3%
Steroids          2011          76          1082-1097
Investigation of new acyloxy derivatives of cholic acid and their esters as drug absorption modifiers
Lech Mr¨®zek, Lenka Dvoř¨¢kov¨¢, Zuzana Mandelov¨¢, Lucie R¨¢rov¨¢, Anna Řez¨¢čov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     daucosterol linoleate
    ÏàËÆ¶È:64.1%
Chinese Pharmaceutical Journal          2007          42          661-663
Studies on Chemical Constituents of Paeonia veitchii L.
WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     14-benzoyldelphonine-8-oleate
C49H75NO9     ÏàËÆ¶È:63.4%
Journal of Natural Products          1994          Vol 57          963
Long-Chain Fatty Acid Esters of Some Norditerpenoid Alkaloids
Yili Bai, Haridutt K. Desai, S. William Pelletier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     balanoinvolin
    ÏàËÆ¶È:63.4%
Journal of Anhui Agricultural Sciences          2012          40          9641-9643
Study on the Chemical Constituents of Mirabilis himalaica Roots
YANG Pan-pan et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     ligustrin A
    ÏàËÆ¶È:63.1%
Phytochemistry          1997          46          977-979
Acylated triterpenoids from Ligustrum ovalifolium
Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     ligustrin B
    ÏàËÆ¶È:62.2%
Phytochemistry          1997          46          977-979
Acylated triterpenoids from Ligustrum ovalifolium
Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     Stigmast-5-en-3¦Â-ol linoleate
C17H18O6     ÏàËÆ¶È:61.5%
Acta Botanica Yunnanica          2001          23(3)          368-372
Chemical Constituents from Dysoxylum hainanense
LUO Xiao-Dong,WU Shao-Hua,MA Yun-Bao,WU Da-Gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     balanoinvolin
C53H90O7     ÏàËÆ¶È:61.5%
Chemistry of Natural Compounds          2009          45          371-373
BALANOINVOLIN, A NEW STEROID DERIVATIVEFROM Balanophora involucrate
Bing Luo, Kun Zou, Zhiyong Guo, Feijun Dan, Juizhi Wang, and Hui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     Ginsenoside DM1
    ÏàËÆ¶È:61.5%
Molecules          2007          12          2140-2150
Isolation, Synthesis and Structures of Cytotoxic Ginsenoside Derivatives
Jun Lei, Xiang Li, Xiao-jie Gong and Yi-nan Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     3¦Â-palmitoyl-11-carboyl-urs-12-ene
C46H78O3     ÏàËÆ¶È:61.5%
Natural Product Research and Development          1997          9(3)          19-23
TRITERPENE ESTERS AND TRITERPENES FROM ILEX KUDINCHA
Ouyang Mingan; Wang Hanqing Su Junhua Liu Yuqing; Yang Chongren
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     daucosterol-6'-linoleate
    ÏàËÆ¶È:60.3%
Journal of Shenyang Pharmaceutical University          2008          25          883-885
Chemical constituents from the seeds of Castanea mollissima Blume(III)
LONG Zhi-min, WU Li-jun, JIANG Bing-ya, SUN Bo-hang, HUANG Jian, GAO Hui-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (3¦Â)-olean-18-en-3-yl stearate
    ÏàËÆ¶È:59.6%
Helvetica Chimica Acta          2007          Vol. 90          652
Triterpene Esters Isolated from Leaves of Maytenus salicifolia Reissek
Roqueline Rodrigues Silva de Miranda, Gr¨¢cia Divina de F¨¢tima Silva, Lucienir Pains Duarte, and SidneyA ugusto Vieira Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     3¦Â-(Stearyloxy)olean-12-ene
C48H84O2     ÏàËÆ¶È:59.6%
Helvetica Chimica Acta          2003          Vol. 86          3445
3¦Â-(Stearyloxy)olean-12-ene from Austroplenckia populnea: Structure Elucidation by 2D-NMR and Quantitative 13C-NMR Spectroscopy
S. A. Vieira Filho, L. P. Duarte, G. D. F. Silva, O. W. Howarth, and I. S. Lula
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     compound 2
C67H116O16     ÏàËÆ¶È:59.6%
Phytochemistry          2008          69          2856-2861
Glycerogalactolipids from the fruit of Lycium barbarum
Zengping Gao, Zulfiqar Ali, Ikhlas A. Khan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     cucurbitacin B esters 2a-c
C48H74O7     ÏàËÆ¶È:59.6%
Journal of Natural Products          2004          67          1823-1828
Cucurbitane Triterpenoids from Leucopaxillus gentianeus
Marco Clericuzio, Mariella Mella, Paola Vita-Finzi, Michele Zema, and Giovanni Vidari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     Ginsenoside PM1
    ÏàËÆ¶È:59.6%
Molecules          2007          12          2140-2150
Isolation, Synthesis and Structures of Cytotoxic Ginsenoside Derivatives
Jun Lei, Xiang Li, Xiao-jie Gong and Yi-nan Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     7¦Â-Hydroxysitosteryl oleate
C47H82O3     ÏàËÆ¶È:59.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     7-ketositosteryl-9,10-dihydroxystearate
C50H86O5     ÏàËÆ¶È:59.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     cholesteryl-9,10 dihydroxystearate
C48H84O4     ÏàËÆ¶È:59.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     7¦Â-Hydroxycholesteryl-9,10-di-tertbutyldimethylsilyloxystearate
C57H108O5Si2     ÏàËÆ¶È:59.6%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     14-benzoyldelphonine-8-palmitate
C47H73NO9     ÏàËÆ¶È:59.6%
Journal of Natural Products          1994          Vol 57          963
Long-Chain Fatty Acid Esters of Some Norditerpenoid Alkaloids
Yili Bai, Haridutt K. Desai, S. William Pelletier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     14-benzoyldelphonine-8-stearate
C49H77NO9     ÏàËÆ¶È:59.6%
Journal of Natural Products          1994          Vol 57          963
Long-Chain Fatty Acid Esters of Some Norditerpenoid Alkaloids
Yili Bai, Haridutt K. Desai, S. William Pelletier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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