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15.4,15.6,15.7,17.4,17.8,25.3,25.4,25.5,25.9,26.2,28.1,28.3,29.9,30.5,33.2,35.2,35.3,38.5,43.1,46.9,47.3,47.4,48.8,48.9,76.7,115.5,123.8,133.3,134.2,176.8
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bravexueli: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-01-07 21:48:23
1 .     trametenolicacid
    ÏàËÆ¶È:76.6%
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   Ì¼Æ×Ä£Äâͼ

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2 .     trametenolic acid B
    ÏàËÆ¶È:73.3%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     methyl trametenolate
    ÏàËÆ¶È:70.9%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     3-keto-tirucall-8,24-dien-21-oicacid
    ÏàËÆ¶È:70%
Chinese Journal of Natural Medicines          2010          8          25-27
Chemical Constituents of Boswellia carterii(Frankincense)
Li Fu-Shuang; YAN Dong-Lan; LIU Rang-Ru; XU Kang-Ping; TAN Gui-Shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     3-oxotirucallic acid
C30H46O3     ÏàËÆ¶È:70%
Zeitschrift f¨¹r Naturforschung C          2003          58          505-516
Immunomodulatory Triterpenoids from the Oleogum Resin of Boswellia carterii Birdwood
F. A. Badria, B. R. Mikhaeil, G. T. Maatooq, and M. M. A. Amer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     10¦Á-cucurbita-5,24-dien-3-ol
    ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          2000          Vol. 83          3191
New Terpenoids from Basidiomycetes Russula lepida
Tan Jian-Wen, Dong Ze-Jun, and Liu Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     trematenolic acid
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2002          50(12)          1603-1606
New Triterpenoids from Tricholoma saponaceum
Kazuko YOSHIKAWA,Mina KUROBOSHI, Shigenobu ARIHARA,Naoko MIURA, Noriyuki TUJIMURA,and Kenji SAKAMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     trametenolic acid
    ÏàËÆ¶È:66.6%
Journal of Natural Products          2005          68          69-73
Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2
Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     antiquol B
C30H50O     ÏàËÆ¶È:66.6%
Journal of Natural Products          2002          65          158-162
Eupha-7,9(11),24-trien-3â-ol (¡°Antiquol C¡±) and Other Triterpenes from Euphorbia antiquorum Latex and Their Inhibitory Effects on Epstein-Barr Virus Activation
Toshihiro Akihisa, E. M. Kithsiri Wijeratne, Harukuni Tokuda, Fumio Enjo, Masakazu Toriumi,Yumiko Kimura, Kazuo Koike, Tamotsu Nikaido, Yasuhiro Tezuka, and Hoyoku Nishino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     trametenolic acid
    ÏàËÆ¶È:66.6%
Planta Medica          1984          50          197-198
3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus
Kirsti Kahlos, R. Hiltunen and M. v. Schantz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     16¦Á-hydroxytrametenolic acid
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1996          44          847-849
Isolation of Inhibitors of TPA-Induced Mouse Ear Edema from Hoelen, Poria cocos
Haruo NUKAYA,Hirokazu YAMASHIRO,Hirotatsu FUKAZAWA,Hitoshi ISHIDA and Kuniro TSUJI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     10-cucurbitadienol
    ÏàËÆ¶È:66.6%
Chinese Chemical Letters          1999          10          297-298
Lepida Acid A from Basidiomycetes Russula lepida
Jian Wen TAN Ji Kai LIU Ze Jun DONG, Pei Gui LIU, Da Gan JI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     10¦Á-cucurbitadienol
    ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          1994          29          39-43
CHEMICAL STUDIES ON RUSSULA ROSACEA
HB Wang; GH Yang; SH Wu; SF; Wang; GY Li; WK Xu; LS Meng and zY Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     pinicolic acid A
C30H46O3     ÏàËÆ¶È:66.6%
Phytochemistry          1999          52          1621-1627
Steroids from the fungus Fomitopsis pinicola
Joachim Rosecke, Wilfried A. Konig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     3-oxo-5¦Á-lanosta-8,24-dien-21-oic acid
    ÏàËÆ¶È:66.6%
Phytochemistry          1997          46          1143-1146
Steroids of formosan Ganoderma tsugae
Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     trametenolic acid B
    ÏàËÆ¶È:66.6%
Phytochemistry          1996          41          1041-1046
Antimicrobial steroids from the fungus Fomitopsis pinicola
Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     inonotsutriol D
C30H50O3     ÏàËÆ¶È:66.6%
Phytochemistry Letters          2011          4          328-332
New lanostane-type triterpenoids, inonotsutriols D, and E, from Inonotus obliquus
Reiko Tanaka, Misaki Toyoshima, Takeshi Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     astrahygrol
C30H48O     ÏàËÆ¶È:66.6%
Phytochemistry          1987          26          2341-2344
Three triterpenes from Astraeus hygrometricus
Yoshihisa Takaishi,Yoshito Murakami,Takashi Ohashi,Kimiko Nakano,Ko¯tarou Murakami,Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     pinnicolic acid A
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2007          38          20-23
Chemical constituents of Stenoloma chusanum
REN Bing-ru; XIA Bing; LI Wei-lin; WU Ju-lan; ZHANG Han-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     3¦Â-hydroxylanosta-8,24-dien-oic acid
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2007          38          20-23
Chemical constituents of Stenoloma chusanum
REN Bing-ru; XIA Bing; LI Wei-lin; WU Ju-lan; ZHANG Han-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     3-Ñõ´úÑòëçÞ-8,24-¶þÏ©-21-ôÈËá
    ÏàËÆ¶È:66.6%
Chinese Journal of Medicinal Chemistry          2003          13          34-37
Isolation and identification of the chemical constituent of Hemerocallis fulva(L.)L.
YANG Zhong-duo, LI Yuan-chao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     trametenolicacid
    ÏàËÆ¶È:66.6%
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   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




23 .     3-oxotirucalla-8,24-dien-21-oicacid
    ÏàËÆ¶È:66.6%
Natural Product Communications          2010          5          1181-1182
Triterpenes from Protium hebetatum Resin
Delcio Dias Marques, Ilmar Bernardo Graebner, Telma Leda Gomes de Lemos,Luciana Lucas Machado, Jõao Carlos Costa Assunção and Francisco Jos¨¦ Queiroz Monte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     3¦Á-hydroxytirucalla-8,24-dien-21-oic acid
    ÏàËÆ¶È:66.6%
Natural Product Communications          2010          5          1181-1182
Triterpenes from Protium hebetatum Resin
Delcio Dias Marques, Ilmar Bernardo Graebner, Telma Leda Gomes de Lemos,Luciana Lucas Machado, Jõao Carlos Costa Assunção and Francisco Jos¨¦ Queiroz Monte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     cycloart-23-ene-3¦Â,25-diol
C30H50O2     ÏàËÆ¶È:66.6%
Research Journal of Phytochemistry          2009          3          18-24
Antihyperglycaemic Activity of Cycloart-23-ene-3¦Â, 25-diol Isolated from Stem Bark of Pongamia pinnata in Alloxan Induced Diabetic Mice
Sachin L. Badole and Subhash L. Bodhankar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     3¦Á-hydroxy-5¦Á-lanosta-8,24-dien-21-oic acid
C32H50O4     ÏàËÆ¶È:65.6%
Phytochemistry          1997          46          1143-1146
Steroids of formosan Ganoderma tsugae
Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     31¦Â-acetoxy-5¦Á-lanosta-8,24-dien-21-oic acid
C32H50O4     ÏàËÆ¶È:65.6%
Phytochemistry          1997          46          1143-1146
Steroids of formosan Ganoderma tsugae
Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




28 .     3¦Á-hydroxy-tirucalla-8,24-dien-21-oate
C31H50O3     ÏàËÆ¶È:64.5%
Phytochemistry          2006          67          1309-1315
Tirucallane triterpenes from the roots of Ozoroa insignis
Yonghong Liu , Pedro Abreu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     methyl 3¦Á,24S-dihydroxytirucalla-8,25-dien-21-oate
C31H50O4     ÏàËÆ¶È:64.5%
Phytochemistry          2006          67          1309-1315
Tirucallane triterpenes from the roots of Ozoroa insignis
Yonghong Liu , Pedro Abreu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     monocarpinine
C31H48O3     ÏàËÆ¶È:64.5%
Journal of Natural Products          2008          71(6)          1104-1106
A Cycloartane Incorporating a Fused Tetrahydrofuran Ring and a Cytotoxic Lactam from Monocarpia marginalis
Siew-Huah Lim, Kamaliah Mahmood, Kanki Komiyama, and Toh-Seok Kam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     Mesendanin P
C31H48O5     ÏàËÆ¶È:64.5%
Helvetica Chimica Acta          2012          95          286-300
Triterpenoids from Melia toosendan
Shi-Hui Dong, Xiu-Feng He, Lei Dong, Yan Wu, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     (24E)-3¦Â-hydroxycucurbita-5,24-diene- 26-oic acid
C30H48O3     ÏàËÆ¶È:63.3%
Helvetica Chimica Acta          2000          Vol. 83          3191
New Terpenoids from Basidiomycetes Russula lepida
Tan Jian-Wen, Dong Ze-Jun, and Liu Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




33 .     fomitopinic acids A
C30H48O5     ÏàËÆ¶È:63.3%
Journal of Natural Products          2005          68          69-73
Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2
Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     3,4-seco-olean-12-ene-3,28-dioic acid
C30H47O4     ÏàËÆ¶È:63.3%
Journal of Natural Products          2000          63          1611-1614
Oleanane Triterpenes from Junellia tridens
Colby G. Caldwell, Scott G. Franzblau, Enrique Suarez,and Barbara N. Timmermann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     3-oxotirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:63.3%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     trametenolic acid
    ÏàËÆ¶È:63.3%
Journal of Natural Products          1999          62          543-545
New Lanostanoid Glycosides from the Fruit Body of Laetiporus versisporus
Kazuko Yoshikawa, Kenji Matsumoto, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     cycloorbigenin A
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1998          34          477-479
TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS LVIII. THE STRUCTURE OF DIHYDROCYCLOORBIGENIN A
M. A. Agzamova and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     3-epicotillol
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1986          22          415-420
GLYCOSYLATION OF TRITERPENOIDS OF THE DAMMARANE SERIES.V. ¦Â-D-GLUCOPYRANOSIDES OF 12¦Â-ACETOXY-20(S),24(R)-EPOXYDAMMARANE- 3¦Á,25-DIOL AND OF 3-EPIOCOTILLOL
L. N. Atopkina, N. F. Samoshina,V. A. Denisenko, N. D. Pokhiio, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     3-epiocotillol
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1981          17          249-253
TRITERPENOIDS FROM THE LEAVES OF FAR EASTERN SPECIES OF THE SHRUBBIRCHES Betula ovalifolia AND B. middendorfii
G. V. Malinovskaya, N. D. Pokhilo, V. V. Makhan'kov, V. L. Novikov, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     lepida acid A
C30H48O3     ÏàËÆ¶È:63.3%
Chinese Chemical Letters          1999          10          297-298
Lepida Acid A from Basidiomycetes Russula lepida
Jian Wen TAN Ji Kai LIU Ze Jun DONG, Pei Gui LIU, Da Gan JI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     arjunic acid
C3OH48O5     ÏàËÆ¶È:63.3%
Journal of Asian Natural Products Research          2001          3          207-212
Triterpene Glycoside from Terminalia Arjuna
R. K. UPADHYAY, M. B. PANDEY, R. N. JHA,V. P. SINGH and V. B. PANDEY
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     euphol (eupha-8,24-di-en-3¦Â-ol)
C30H50O     ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2006          31          742-744
Studies on constituents from roots of Euphorbia hylonoma
RUAN Hanli, ZHANG Yue, ZHANG Yonghui, PI Huifang, WU Jizhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     cycloartenol
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2003          28          1040-1042
Studies on Chemical Constituents in of Ervatamia hainanensis
TAN Xingqi, CHEN Haisheng, XU Congli, LIU Runhui, XUAN Weidong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     pinicolic acid E
    ÏàËÆ¶È:63.3%
Phytochemistry          2000          54          603-610
Constituents of various wood-rotting basidiomycetes
Joachim Rösecke, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     3-oxo-tirucalla-7,24-dien-21-al
C30H46O2     ÏàËÆ¶È:63.3%
Phytochemistry          1998          49          2457-2460
Triterpenoids from Owenia cepiodora
Dulcie A. Mulholland, Maria Kotsos, Hamdani A. Mahomed, David A. H. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     cabraleadiol
    ÏàËÆ¶È:63.3%
Phytochemistry          1997          46          1139-1141
Dammarane-type triterpenes from Cordia spinescens
Norio Nakamura, Shiho Kojima, Yasmina Aura Lim, Meselhy R. Meselhy, Masao Hattori, Mahabir P. Gupta, Mireya Correa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     boeticol
C30H50O     ÏàËÆ¶È:63.3%
Journal of Natural Products          1995          Vol 58          275-279
Boeticol, a New Tetracyclic Triterpene from Euphorbia boetica
Maria Jos¨¦ U. Ferreira, Jos¨¦ R. Ascenso, Olga S. Tavares
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     4¦Á,14¦Á-dimethyl-cholesta-8,24-dien-3¦Â-ol
    ÏàËÆ¶È:63.3%
Phytochemistry          1996          41          1191-1195
Antibacterial hydroperoxysterols from Xanthosoma robustum
Takeshi Kato, Barbara Frei, Michael Heinrich, Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     21-hydroxylanosta-8,24-dien-3-one
    ÏàËÆ¶È:63.3%
Phytochemistry          1996          41          1041-1046
Antimicrobial steroids from the fungus Fomitopsis pinicola
Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     trametenolic acid
C30H48O3     ÏàËÆ¶È:63.3%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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51 .     3-epi-astrahygrol
C30H48O     ÏàËÆ¶È:63.3%
Phytochemistry          1987          26          2341-2344
Three triterpenes from Astraeus hygrometricus
Yoshihisa Takaishi,Yoshito Murakami,Takashi Ohashi,Kimiko Nakano,Ko¯tarou Murakami,Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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52 .     31-nor-9¦Â,19-cyclolanost-24-en-3¦Â-ol
C29H48O     ÏàËÆ¶È:63.3%
Phytochemistry          1990          29          994-997
Cycloartane derivatives from Garcinia lucida
Anne-Marie Nyemba,Theophile Ngando Mpondo,Joseph D. Connolly,David S. Rycroft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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53 .     Cabraleadiol
C30H52O3     ÏàËÆ¶È:63.3%
Phytochemistry          1985          24          2925-2928
Dammarane Triterpenes from the stem bark of Commiphora Dalzielii
Peter G. Waterman, Stephen Ampofo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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54 .     betulafolienetriol
    ÏàËÆ¶È:63.3%
Phytochemistry          2010          71          877-894
Fatty acid derivatives and dammarane triterpenes from the glandular trichome exudates of Ibicella lutea and Proboscidea louisiana
Teigo Asai, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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55 .     lanosterol
C30H50O     ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2005          36          1763-1767
Ingenane diterpene ester constituents from Tibetan medicine Euphorbia wallichii
LI Yu-lin; SUO You-rui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




56 .     ¶¹çÞ´¼-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2002          33          300-303
Studies on chemical constituents in seed of Litchi chinensis
TU Peng fei; LUO Qing; ZHENG Jun hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




57 .     3¦Â-dihydroxy-lanosta-8,24-diene-21-acid
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2001          32          4-6
Studies on chemical constituents of Fuscoporia obliqua
HE Jian; FENG Xiao zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




58 .     cabraleadiol
C30H52O3     ÏàËÆ¶È:63.3%
Chinese Journal of Natural Medicines          2010          8          270-273
Chemical Constituents from the Roots of Dysoxylum densiflorum
LI Chang-Song; YU Hong-Wei; LI Guo-You; ZHANG Guo-Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




59 .     cabraleahydroxylactone
C27H44O3     ÏàËÆ¶È:63.3%
Chinese Journal of Natural Medicines          2010          8          270-273
Chemical Constituents from the Roots of Dysoxylum densiflorum
LI Chang-Song; YU Hong-Wei; LI Guo-You; ZHANG Guo-Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




60 .     Cabraleadiol
    ÏàËÆ¶È:63.3%
Archives of Pharmacal Research          2008          31          21-27
A new sesquiterpene and other terpenoid constituents of Chisocheton penduliflorus
Jarinporn Phongmaykin, Takuya Kumamoto, Tsutomu Ishikawa, Rutt Suttisri and Ekarin Saifah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




61 .     Cycloartenol
C26H34O11     ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          2010          46          459-461
Chemical investigation of Ervatamia yunnanensis
Jing-Ling Du, Yong-Sheng Jin, Li-Ming Qiao, Li Jin and Hai-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




62 .     3¦Â-ôÇ»ùÑòëçÞ-8,24-¶þÏ©-21-ôÈËá
    ÏàËÆ¶È:63.3%
Chinese Journal of Medicinal Chemistry          2003          13          34-37
Isolation and identification of the chemical constituent of Hemerocallis fulva(L.)L.
YANG Zhong-duo, LI Yuan-chao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




63 .     reissantenol oxide
C30H50O2     ÏàËÆ¶È:63.3%
Journal of the Chemical Society, Perkin Transactions 1          1989                   2259-2267
Studies on terpenoids and steroids. Part 19. Structures of three novel 19(10¡ú9)abeo-8¦Á,9¦Â,10¦Á-euphane triterpenoids from Reissantia indica(Celastraceae)
Chandra B. Gamlath, A. A. Leslie Gunatilaka and Suganthini Subramaniam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




64 .     24-oxoreissant-5-ene-3¦Â,25-diol
C30H50O3     ÏàËÆ¶È:63.3%
Journal of the Chemical Society, Perkin Transactions 1          1989                   2259-2267
Studies on terpenoids and steroids. Part 19. Structures of three novel 19(10¡ú9)abeo-8¦Á,9¦Â,10¦Á-euphane triterpenoids from Reissantia indica(Celastraceae)
Chandra B. Gamlath, A. A. Leslie Gunatilaka and Suganthini Subramaniam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




65 .     lanosterol
    ÏàËÆ¶È:63.3%
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   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




66 .     Epilupeol
    ÏàËÆ¶È:63.3%
Journal of Chinese Pharmaceutical Sciences          2010          19          387-392
Assignment of the absolute stereochemistry of an unusual diterpenoid from the mangrove plant Excoecaria agallocha L.
Zhen Liu; Wei Jiang; Zhi-Wei Deng; Wen-Han Lin*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




67 .     compound 2a
C39H53NO5     ÏàËÆ¶È:62.8%
Phytochemistry          1993          32          1239-1244
Triterpenes of Poria cocos
Takaaki Tai, Akira Akahori, Tetsuro Shingu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




68 .     antiquol B acetate
C32H52O2     ÏàËÆ¶È:62.5%
Journal of Natural Products          2002          65          158-162
Eupha-7,9(11),24-trien-3â-ol (¡°Antiquol C¡±) and Other Triterpenes from Euphorbia antiquorum Latex and Their Inhibitory Effects on Epstein-Barr Virus Activation
Toshihiro Akihisa, E. M. Kithsiri Wijeratne, Harukuni Tokuda, Fumio Enjo, Masakazu Toriumi,Yumiko Kimura, Kazuo Koike, Tamotsu Nikaido, Yasuhiro Tezuka, and Hoyoku Nishino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




69 .     methyl 3¦Á,25-dihydroxy-tirucalla-8-ene-21-oate
C31H52O4     ÏàËÆ¶È:61.2%
Phytochemistry          2006          67          1309-1315
Tirucallane triterpenes from the roots of Ozoroa insignis
Yonghong Liu , Pedro Abreu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




70 .     fuscoporianol A
C31H52O3     ÏàËÆ¶È:61.2%
Journal of Asian Natural Products Research          2001          3          55-61
Three New Triterpenoids from Fuscoporia Obliqua
JJAN HE, XIAO-ZHANG FENG, YANG LU and BIN ZHAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




71 .     methyl 3¦Á-hydroxyolean-18-en-28-oate
C31H40O3     ÏàËÆ¶È:61.2%
Phytochemistry          1995          39          99-103
Terpenoids from the liverworts Symphyogyna brasiliensis and unidentified Frullania species
Motoo Tori, Mamiko Aoki, Katsuyuki Nakashima, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




72 .     compound 1
C31H50O3     ÏàËÆ¶È:61.2%
Chinese Journal of Chemistry          2001          19          702-704
A Novel Lanostanoid Lactone From the Alga Hypnea cerricornis
Xiao-Hua Xu, Xiao Chen, Jian-Hua Lu, Guang-Min Yao, Yan-Ming Li and Long-Mei Zeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




73 .     3¦Á,20(S)-Dihydroxy-25-methoxy-dammar-23-ene
C31H54O3     ÏàËÆ¶È:61.2%
Journal of Natural Medicines          2011          65          217-223
Seven new dammarane triterpenes from the floral spikes of Betula platyphylla var. japonica
Juan Xiong ,Masatoshi Taniguchi ,Yoshiki Kashiwada ,Takashi Yamagishi ,Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




74 .     methyl 3¦Á-acetyloxylanosta-8,24-dien-21-oate
    ÏàËÆ¶È:60.6%
Phytochemistry          1996          41          1041-1046
Antimicrobial steroids from the fungus Fomitopsis pinicola
Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




75 .     meiogynin A
C38H50O4     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          480-483
A Dimeric Sesquiterpenoid from a Malaysian Meiogyne as a New Inhibitor of Bcl-xL/BakBH3 Domain Peptide Interaction
Marc Litaudon, Hadjira Bousserouel, Khalijah Awang, Olivier Nosjean, Marie-Therese Martin,Marie Elise Tran Huu Dau, Hamid A Hadi, Jean A. Boutin, Thierry Sevenet, and Franc¸oise Gueritte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




76 .     inonotsutriol A
C30H50O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2008          Vol. 91          1513
Three New Lanostane Triterpenoids, Inonotsutriols A, B, and C, from Inonotus obliquus
Sayaka Taji, Takeshi Yamada, and Reiko Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




77 .     (3¦Â,11¦Â)-3,11-dihydroxylanosta-8,24-dien-7-one
C30H48O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2007          Vol. 90          2245
Four New Lanostane Triterpenoids from Euphorbia humifusa
Zhi-Qiang Lu, Guang-Tong Chen, Jin-Qiang Zhang, Hui-Lian Huang, Shu-Hong Guan, and De-An Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




78 .     (24E)-3,4-secocucurbita-4,24-diene-3,26,29-trioic acid
C30H46O6     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2000          Vol. 83          3191
New Terpenoids from Basidiomycetes Russula lepida
Tan Jian-Wen, Dong Ze-Jun, and Liu Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




79 .     (-)-(23E),25-hydroperoxytirucalla-8,23-dien-3¦Â-ol-7-one
C30H48O4     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          1620-1626
Chemical Constituents of the Roots of Euphorbia micractina
Wendong Xu, Chenggen Zhu, Wei Cheng, Xiaona Fan, Xiaoguang Chen, Sen Yang, Ying Guo, Fei Ye, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




80 .     3¦Â-hydroxy-29-norcycloart-24-one
C29H48O2     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2001          49(2)          183-187
Triterpenes and Lignans from Artemisia caruifolia and Their Cytotoxic Effects on Meth-A and LLC Tumor Cell Lines
Chao-mei MA, Norio NAKAMURA, Byung Sun MIN, and Masao HATTORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




81 .     11¦Â,21¦Â-dihydroxy-olean-12-ene-3-one
C30H48O3     ÏàËÆ¶È:60%
Phytochemistry          2008          69          1057-1064
21¦Â-Hydroxy-oleanane-type triterpenes from Hippocratea excelsa
David C¨¢ceres-Castillo, Gonzalo J. Mena-Rej¨®n,Roberto Cedillo-Rivera, Leovigildo Quijano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




82 .     3¦Á,24R,25-trihydroxytirucall-8-en-21-oic acid
C30H50O5     ÏàËÆ¶È:60%
Phytochemistry          2006          67          1309-1315
Tirucallane triterpenes from the roots of Ozoroa insignis
Yonghong Liu , Pedro Abreu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




83 .     11¦Á-hydroxy-epi-betulin
C30H50O3     ÏàËÆ¶È:60%
Journal of Natural Products          2005          68          1018-1021
Lupane Triterpenoids from Maytenus Species
Marvin J. Nez, Carolina P. Reyes, Ignacio A. Jimnez, Laila Moujir, and Isabel L. Bazzocchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




84 .     acridocarpusic acid D
C30H47O2     ÏàËÆ¶È:60%
Journal of Natural Products          2004          67          986-989
Cytotoxic Triterpenoids from Acridocarpus vivy from the Madagascar Rain Forest
Shugeng Cao, Rebecca Clare Guza, James S. Miller, Rabodo Andriantsiferana, Vincent E. Rasamison, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




85 .     3,23-disulfate ester of rotundic acid
C30H48O11S2     ÏàËÆ¶È:60%
Journal of Natural Products          2007          70          1889-1894
Triterpene, Antioxidant, and Antimicrobial Compounds from Melissa officinalis
Teresa Mencherini,Patrizia Picerno, Carla Scesa, and Rita Aquino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




86 .     dubione A
C30H44O4     ÏàËÆ¶È:60%
Journal of Natural Products          2002          65          1886-1891
Antineoplastic Agents. 489. Isolation and Structures of Meliastatins 1-5 and Related Euphane Triterpenes from the Tree Melia dubia1
George R. Pettit,Atsushi Numata,Chika Iwamoto, Hideaki Morito, Takeshi Yamada,Animesh Goswami,Paul J. lewlow, Gordon M. Cragg, and Jean M. Schmidt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




87 .     2¦Á,3¦Á,19¦Á-trihydroxy-12-oleanen-28-oic acid
C30H48O5     ÏàËÆ¶È:60%
Journal of Natural Products          2001          64          865-869
Monoterpene Glycosides and Triterpene Acids from Eriobotrya deflexa
Tzong-Huei Lee,Shoei-Sheng Lee, Yuh-Chi Kuo, and Chang-Hung Chou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




88 .     compound 4
C30H50O2     ÏàËÆ¶È:60%
Journal of Natural Products          2000          63          514-516
New Lanostanoids of Ganoderma tsugae
Huey-Jen Su,Yih-Fen Fann,Mei-Ing Chung, Shen-Jeu Won, and Chun-Nan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




89 .     alertenone
C30H44O2     ÏàËÆ¶È:60%
Journal of Natural Products          1999          62          633-635
Alertenone, a Dimer of Suberosenone from Alertigorgia sp.
Heidi R. Bokesch, John W. Blunt, Chandra K. Westergaard, John H. Cardellina II, Tanya R. Johnson, Jennifer A. Michael, Tawnya C. McKee, Melinda G. Hollingshead, and Michael R. Boyd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




90 .     argenteanol D
C30H50O3     ÏàËÆ¶È:60%
Journal of Natural Products          1997          60          81-85
Argenteanones C-E and Argenteanols B-E, Cytotoxic Cycloartanes from Aglaia argentea
K. Mohamad, M.-T. Martin, E. Leroy, C. Temp¨ºte, T. S¨¦venet, K. Awang, and M. Païs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




91 .     lupenone (1), 3-epi-lupeol
    ÏàËÆ¶È:60%
Planta Medica          2005          71          208-213
Cytotoxic Activity of Lupane-Type Triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum Two of which Induce Apoptosis
Puapairoj, Prapawadee; Naengchomnong, Waree; Kijjoa, Anake; Pinto, Madalena M.; Pedro, Madalena; Nascimento, Maria São Jos¨¦; Silva, Artur M. S.; Herz, Werner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




92 .     3¦Á,12¦Â,20(S)-protopanasadiol
    ÏàËÆ¶È:60%
Planta Medica          1993          59          76-79
Saponins in the Leaves of Birch? Hemolytic Dammarane Triterpenoid Esters of Betula pendula
Burlc hard Rickling and Karl- Werner Glombitza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




93 .     29-nor-cycloartan-24,25-epoxy-3¦Â-ol
C29H48O2     ÏàËÆ¶È:60%
Planta Medica          1988          54          40-41
New Cycloartenol Derivatives from Aglaia roxburghiana
S. P. Vishnoi, A. Shoeb, and R. S. Kapil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




94 .     tirucalla-5,7,24-trien-3¦Â-ol
C30H48O     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1997          45          2016-2023
Triterpene Alcohols from Camellia and Sasanqua Oils and Their Anti-inflammatory Effects
Toshihiro AKIHISA,Ken YASUKAWA,Yumiko KIMURA,Sei-ichi TAKASE,Sakae YAMANOUCHI and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




95 .     3¦Â,16¦Á-dihydroxylanosta-7,9(11),24-trien-21-oic acid
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1996          44          847-849
Isolation of Inhibitors of TPA-Induced Mouse Ear Edema from Hoelen, Poria cocos
Haruo NUKAYA,Hirokazu YAMASHIRO,Hirotatsu FUKAZAWA,Hitoshi ISHIDA and Kuniro TSUJI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




96 .     3-epi-ocotillol
C30H52O3     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1996          44          1748-1753
Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




97 .     methyl azizate
C32H50O6     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1979          27          2874-2876
Chemische Untersuchungen der Inhaltsstoffe von Arachinoides standishii OHWI
NOBUTOSHI TANAKA,HARUKA MAEHASHI,SUMIE SAITO,TAKAO MURAKAMI,YASUHISA SAIKI,CHIUMING CHEN and YOICHI IITAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




98 .     4¦Á,14-dimethyl-9,19-cyclocholestan-3¦Â,24¦Î-diol
C29H50O2     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1982          30          2780-2786
Studies on the Constituents of Pollen. X. On the Constituents of Pollen Grains of Ambrosia elatior LINNE (2)
TAICHI OHMOTO,KEIJI IKEDA and TAKEO CHIBA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




99 .     4¦Á,14-dimethyl-9,19-cyclocholestan-3¦Â,24¦Î,25-triol
C29H50O3     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1982          30          2780-2786
Studies on the Constituents of Pollen. X. On the Constituents of Pollen Grains of Ambrosia elatior LINNE (2)
TAICHI OHMOTO,KEIJI IKEDA and TAKEO CHIBA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




100 .     A-nor-3-Oxo-5¦ÂH-olean-12-en-30-oic Acid
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2006          42          553-557
SYNTHESIS AND HIGH-RESOLUTION NMR SPECTRA OF A-nor-DERIVATIVES OF 11-DEOXYGLYCYRRHETIC ACID
L. R. Mikhailova, L. A. Baltina, R. M. Kondratenko,. Kunert,L. V. Spirikhin,F. Z. Galin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




101 .     Thalicogenin
C30H50O4     ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2005          41          117-140
STRUCTURAL STUDIES AND BIOLOGICAL ACTIVITY OF PLANT TRITERPENOIDS FROM THE Thalictrum GENUS
V. I. Lutskii, A. S. Gromova,E. A. Khamidullina, and N. L. Owen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




102 .     Azizic acid
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




103 .     22¦Á-Hydroxyerythrodiol
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




104 .     compound 10
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1985          21          328-332
TRITERPENOIDS FROM THE LEAVES OF THE SIBERIAN SPECIES OF BIRCH Betula nana and B. exilis
N. D. Pokhilo, G. V. Malinovskaya, V. V. Makhan'kov, V. A. Denisenko, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------
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