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1 . 11-hydroxy-12-methoxyabieta-8,11,13-triene-3,7-dione ÏàËÆ¶È:61.5% Journal of Shenyang Pharmaceutical University 2009 26 956-961 Isolation and identification of chemical constituents from Taxus cuspidta Sibe. et Zucc. LI Ya-nan, WANG Wen-ze, WU Li-jun, WANG Ji-wen, GAO Hui-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (-)-agelasine D C26H41N5O ÏàËÆ¶È:57.6% Bioorganic & Medicinal Chemistry 2010 18 1297-1311 From anti-fouling to biofilm inhibition: New cytotoxic secondary metabolites from two Indonesian Agelas sponges Triana Hertiani, RuAngelie Edrada-Ebel, Sofia Ortlepp, Rob W.M. van Soest, Nicole J. de Voogd, Victor Wray, Ute Hentschel, Svetlana Kozytska, Werner E.G. M¨¹ller, Peter Proksch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 3 C28H40O4 ÏàËÆ¶È:57.1% Phytochemistry 1985 24 1047-1050 Tetraprenyltoluquinols from the brown alga Cystoseira jabukae Vincenzo Amico, Francesca Cunsolo, Mario Piattelli, Giuseppe Ruberto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Macrocarpoic acid B C30H46O4 ÏàËÆ¶È:56.6% Natural Product Communications 2006 1 1073-1078 Triterpenes from Maytenus macrocarpa and Evaluation ofTheir Anti-HIV Activity Sonia Piacente, Lourdes Campaner Dos Santos, Naheed Mahmood and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Sumaresinolic acid C30H48O4 ÏàËÆ¶È:56.6% Natural Product Communications 2009 4 1323-1326 Triterpenes from Warszewiczia coccinea (Rubiaceae) asInhibitors of Acetylcholinesterase Angela I. Calder¨®n, Johayra Simithy, Giuliana Quaggio, Alex Espinosa,Jose Luis L¨®pez-P¨¦rez and Mahabir P. Gupta Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ÆÑ¹«Ó¢çÞ´¼ ÏàËÆ¶È:55.5% Journal of Shenyang Pharmaceutical University 2008 25 623-626 Chemical constituents of the stems and leaves of Calophyllum inophyllum LIU Dan, LI Zhan-lin, LI Yan-zhi, HUA Hui-ming, LIU Ming-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 2¦Á-Hydroxyurs-12-en-28-oic acid C30H48O3 ÏàËÆ¶È:55.1% Journal of Natural Products 2009 72 1414-1418 Synthesis of 3-Deoxypentacyclic Triterpene Derivatives as Inhibitors of Glycogen Phosphorylase Pu Zhang,Jia Hao,Jun Liu,Qian Lu, Huaming Sheng, Luyong Zhang, and Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-oxo-20S-hydroxytaraxastane C30H52O2 ÏàËÆ¶È:55.1% Fitoterapia 2001 72 709-711 Triterpenes from the resin of Protium heptaphyllum G.S. Susunaga, A.C. Siania, M.G. Pizzolatti,R.A. Yunes, F. Delle Monache Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 11¦Â-hydroxydihydrocedrelone C26H32O6 ÏàËÆ¶È:53.8% Journal of Natural Products 2000 63 947-951 Tetranortriterpenoids from Walsura yunnanensis Xiao-Dong Luo, Shao-Hua Wu, Yun-Bao Ma, and Da-Gang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Isopseudolarifuroic acid B C26H40O3 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry Letters 2001 11 3119-3122 Two Novel Cytotoxic and Antimicrobial Triterpenoids from Pseudolarix kaempferi Sheng-Ping Yang, Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . agelasine-D C26H39N5 ÏàËÆ¶È:53.8% Bulletin of the Chemical Society of Japan 1986 59 2495-2504 Structures of Agelasines, Diterpenes Having a 9-Methyladeninium Chromophore Isolated from the Okinawan Marine Sponge Agelas nakamurai Hoshino Houming Wu, Hideshi Nakamura, Jun¡¯ichi Kobayashi, Masaki Kobayashi, Yasushi Ohizumi, Yoshimasa Hirata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . amphidinolide T4 C25H42O5 ÏàËÆ¶È:53.8% The Journal of Organic Chemistry 2001 66 134-142 Amphidinolides T2, T3, and T4, New 19-Membered Macrolides from the Dinoflagellate Amphidinium sp. and the Biosynthesis of Amphidinolide T1 Jun'ichi Kobayashi, Takaaki Kubota, Tetsuya Endo, and Masashi Tsuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 19 ÏàËÆ¶È:53.8% Journal of Agricultural and Food Chemistry 2008 56 2985-2988 Preparation and Phytotoxicity of Novel Kaurane Diterpene Amides with Potential Use as Herbicides Maria Am¨¦lia Diamantino Boaventura, Rondinelle Gomes Pereira, Luiza B. de Oliveira Freitas, Leandro Alves dos Reis and Henriete da Silva Vieira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . floridenol C25H42O ÏàËÆ¶È:53.8% Journal of the American Chemical Society 1981 103 7009-7011 Unusual sesterterpenoids from the secretion of Ceroplastes floridensis (Coccidae), an orchard pest. Application of the allylic benzoate method for determination of absolute configuration Yoko Naya, Kazuo Yoshihara, Takashi Iwashita, Hajime Komura, Koji Nakanishi, Yasuo Hata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . foliasalaci B1 C30H50O2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2008 56(7) 915-920 Hnew Triterpene Constituents, Foliasalacins A1¡ªA4, B1¡ªB3, and C, from the Leaves of Salacia chinensis Masayuki YOSHIKAWA,Yi ZHANG, Tao WANG, Seikou NAKAMURA, and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 22¦Â,29-dihyroxy-12-oleanen-3-one C30H48O3, ÏàËÆ¶È:53.3% Journal of Natural Products 2008 71(11) 1829-1832 Triterpenoids and Aromatics from Derris laxiflora Hsi-Lin Chiu, Jyh-Horng Wu, Yu-Tang Tung, Tzong-Huei Lee, Shin-Chang Chien, and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 3-O-acetyldaturadiol ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 1379-1384 Activity of Triterpenoid Glycosides from the Root Bark of Mussaenda macrophylla against Two Oral Pathogens Nam-Cheol Kim, Anne E. Desjardins, Christine D. Wu, and A. Douglas Kinghorn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 29-hydroxy-3-oxo-olean-12-en-28-oic acid C30H46O4 ÏàËÆ¶È:53.3% Phytochemistry 2000 53 805-810 Triterpenoids from Tripterygium wilfordii Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto, Takao Taki, Yongfeng Jia , Duan Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . methylsumaresinolate ÏàËÆ¶È:53.3% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . methyl-3-episumaresinolate ÏàËÆ¶È:53.3% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 21-oxo-3,4-seco-olean-4(23)-12-dien-3-oic acid C30H46O3 ÏàËÆ¶È:53.3% Phytochemistry 1991 30 1221-1223 Seco ring-A triterpene acids from the resin of Dacryodes normandii Ian C. Parsons, Alexander I. Gray, Peter G. Waterman, Catherine Lavaud, Georges Massiot Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . ÐܹûËá(ursolic acid) ÏàËÆ¶È:53.3% Chinese Traditional and Herbal Drugs 2011 42(5) 841-843 Chemical constituents in root of Actinidia chinensis CHEN Xiao-xiao, YANG Shang-jun, BAI Shao-yan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . sumresinolic C30H48O4 ÏàËÆ¶È:53.3% Natural Product Research and Development 2009 21 242-245 Study on Chemical Constituents of Uncaria rhynchophylla DENG Mei-cai; JIAO Wei; DONG Wei-wei; YANG Chun-bin; LU Run-hua Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . hongdoushan C C27H42O6 ÏàËÆ¶È:51.8% Journal of Natural Products 2002 65 1700-1702 Three New C-14 Oxygenated Taxanes from the Wood of Taxus yunnanensis Arjun H. Banskota, Tepy Usia, Yasuhiro Tezuka, Kyoji Kouda, Nhan Trung Nguyen, and Shigetoshi Kadota Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 3-(11'-Carboxy-3',7',15'-trimethylhexadecyl)-4,5-dihydroxybenzoic acid C31H44O6 ÏàËÆ¶È:51.8% Phytochemistry Letters 2009 2 119-112 Caldensinic acid, a prenylated benzoic acid from Piper caldense Giovana C. Freitas, Rodrigo O. Saga Kitamura, João Henrique G. Lago, Maria Claudia M. Young, Elsie F. Guimarães, Massuo J. Kato Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . ent-methylisoozate dimer C42H64O4 ÏàËÆ¶È:51.8% Phytochemistry 1999 51 813-817 Labdane dimers from Xylopia aromatica Dirceu Martins, Lidilhone Hamerski, Sandra A.V. Alvarenga, Nidia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . urs-12(13)-en-3-on-28-oic acid ÏàËÆ¶È:51.8% Acta Scientiarum Naturalium Universitatis Sunyatseni 1996 35(S2) 40-44 Studies on the Chemical Constituents of the Lu Lu Tong(2) Lai Zuoqi, Dong Yong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . oleanolic acid ÏàËÆ¶È:51.7% Chinese Traditional and Herbal Drugs 2011 42 230-233 Chemical constituents of Limonium sinense LIU Xing-kuan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . methyl 3-epi-sumaresinolate C31H50O4 ÏàËÆ¶È:51.6% Journal of Natural Products 1992 Vol 55 963 Triterpenes from Miconia stenostachya Wilfred R. Chan, Veronica Sheppard, Kathleen A. Medford, Winston F. Tinto, William F. Reynolds, Stewart McLean Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . oleanolic aldehyde acetate ÏàËÆ¶È:51.6% Korean Journal of Pharmacognosy 2010 41 97-102 Inhibition of IL-6 Production in TNF- Stimulated MG-63 by the Triterpenoids Isolated from Aucuba japonica Jin, Qinglong; Jin, Hong-Guang; Shin, Ji-Eun; Choi, Eun-Jin; Woo, Eun-Rhan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . oleanolic aldehyde acetate ÏàËÆ¶È:51.6% Korean Journal of Pharmacognosy 2010 41 97-102 Inhibition of IL-6 Production in TNF-¦Á Stimulated MG-63 by the Triterpenoids Isolated from Aucuba japonica Qinglong Jin, Hong-Guang Jin, Ji Eun Shin, Eun Jin Choi and Eun-Rhan Woo Structure 13C NMR ̼Æ×Ä£Äâͼ |

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