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²éѯ½á¹û£º¹²²éµ½4901¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 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 -------------------------------------------------------------------------------- 2 . astrahygrol C30H48O ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 3 . trametenolicacid ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 4 . ¦Â-amyrin ÏàËÆ¶È:70% Asian Journal of Traditional Medicines 2007 2 135-139 A new cassane diterpene from Caesalpinia bonduc (fabaceae) Zhaohua Wu , Yongyi Wang , Jian Huang , Bohang Sun and Lijun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 31¦Â-acetoxy-5¦Á-lanosta-8,24-dien-21-oic acid C32H50O4 ÏàËÆ¶È:68.7% 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 -------------------------------------------------------------------------------- 6 . 3¦Á-hydroxy-tirucalla-8,24-dien-21-oate C31H50O3 ÏàËÆ¶È:67.7% Phytochemistry 2006 67 1309-1315 Tirucallane triterpenes from the roots of Ozoroa insignis Yonghong Liu , Pedro Abreu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . meiogynin A C38H50O4 ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 8 . inonotsutriol A C30H50O3 ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 9 . sootepin B C30H44O4 ÏàËÆ¶È:66.6% Journal of Natural Products 2009 72 1161-1164 Cytotoxic 3,4-seco-Cycloartane Triterpenes from Gardenia sootepensis Thanesuan Nuanyai, Reungrit Sappapan, Thapong Teerawatananond, Nongnuj Muangsin,and Khanitha Pudhom Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3¦Á,21¦Â-dihydroxy-olean-12-ene C30H50O2 ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 11 . ¦Â-amyrin ÏàËÆ¶È:66.6% Phytochemistry 2005 66 1759-1766 Cloning and characterization of a cDNA encoding b-amyrin synthase from petroleum plant Euphorbia tirucalli L. Masataka Kajikawa, Katsuyuki T. Yamato, Hideya Fukuzawa, Yasuyoshi Sakai,Hidenobu Uchida, Kanji Ohyama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 2¦Á,3¦Â-dihydroxy-olean-28-oic acid C30H50O4 ÏàËÆ¶È:66.6% Planta Medica 2006 72 643-649 New Polyhydroxylated Triterpenes and Anti-Inflammatory Activity of Salvia hierosolymitana A. De Felice,A. Bader,A. Leone,S. Sosa,R. Della Loggia,A. Tubaro,N. De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3¦Â-hydroxy-lanosra-8,24-dien-21-al 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 -------------------------------------------------------------------------------- 14 . amyrin ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1987 35 1610-1614 Studies on the Constituents of Goat's Rue (Galega officinalis L.) TAKEHIKO FUKUNAGA,KOICHI NISHIYA,KOICHI TAKEYA and HIDEJI ITOKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . ¦Â-amyrin C30H50O ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2009 45 921-924 ISOPRENOIDS OF Euphorbia sororia. I. TRITERPENOIDS Y. Huang,H. A. Aisa, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . L-H1 ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1996 32 360-365 TRITERPENE GLYCOSIDES OF Hedera canariensis.I. STRUCTURES OF GLYCOSIDES L-A, L-B1, L-B 2, L-C, L-D,L-E 1, L-G 1, L-G 2, L-G 3, L-G4, L-H1, L-H2, AND L-I 1 FROM THE LEAVES OF Hedera canariensis V. I. Grishkovets, D. Yu. Sidorov, L. A. Yakovishin, N. N. Arnautov, A. S. Shashkov and V. Ya. Chirva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Abrisapogenol F ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . ¦Â-amyrin C30H50O ÏàËÆ¶È:66.6% Acta Bot. Boreal. -Occident. Sin. 2007 27 1141-1146 The Triterpenes in Salvia umbratica LIU Qing, LIU Zhen-ling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . ¦Á-amyrin [12-ursen-3¦Â-ol] C30H50O ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2003 5 35-41 IRRITANT POTENTIAL OF SOME CONSTITUENTS FROM THE SEEDS OF CAESALPINIA BONDUCELLA (L.) FLEMING M. ASIF SAEED and A.W. SABIR Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . ¦Â-amyrin C30H50O ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2006 31 1875-1879 Triterpenes from herb of Potentilla chinesis LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . ¦Â-amyrin ÏàËÆ¶È:66.6% Phytochemistry 1999 52 723-730 Flavonoids from the root-bark of Dioclea grandiflora |
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