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