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kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-11-26 13:37:33
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kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-11-26 13:37:33
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½4810¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3¦Â-hydroperoxy-7¦Â,25-epoxy-D:B-friedoolean-5-ene C30H48O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2009 72 1045-1048 Triterpenoids and a Lignan from the Aerial Parts of Maytenus apurimacensis Nabil E. J. Vazdekis, Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, and ¨¢ngel G. Ravelo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . pomolic acid ÏàËÆ¶È:66.6% Natural Product Sciences 2007 13 152-159 The Anti-hyperlipidemic Effect and Constituents of the 19-Hydroxyursane-type Triterpenoid fraction Obtained from the Leaves of Rusus crataegifolius Nam, Jung-Hwan; Jung, Hyun-Ju; Tapondjou, Leon Azefack; Lee, Kyung-Tae; Choi, Jong-Won; Kim, Won-Bae; Park, Hee-Juhn Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ursolic acid ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 1999 30(3) 161-164 Studies on the Chemical Constituents of Shady Jerusalemsage (Phlomis umbrosa)(¢ñ) Liu Shiwang; Fu Hongzheng and Lin Wenhan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 21¦Á-hydroxy ursolic acid ÏàËÆ¶È:66.6% Natural Product Research and Development 1997 9(2) 4-6 NON-ALKALOIDAL CONSTITUENTS FROM MECONOPSIS PUNICEA MAXIM Zhang Guolin; Li Bogang; Zhou Zhengzhi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (23E)-25-methoxycucurbit-23-ene-3¦Â,7¦Â-diol C31H52O3 ÏàËÆ¶È:64.5% Journal of Natural Products 2006 69 1168-1171 Cucurbitane-Type Triterpenoids from Momordica charantia Chi-I Chang, Chiy-Rong Chen, Yun-Wen Liao, Hsueh-Ling Cheng, Yo-Chia Chen, and Chang-Hung Chou Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 20¦Â,28-epoxy-28¦Á-methoxytaraxasteran-3¦Â-ol C31H52O3 ÏàËÆ¶È:64.5% Journal of Natural Products 2006 69 1164-1167 Taraxasterane- and Ursane-Type Triterpenes from Nerium oleander and Their Biological Activities Ming Zhao, Shujun Zhang, Liwei Fu, Na Li, Jiao Bai, Junichi Sakai, Liyan Wang, Wanxia Tang, Toshiaki Hasegawa, Hirotsugu Ogura, Takao Kataoka, Seiko Oka, Miwa Kiuch, Katutoshi Hirose, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 21-dehydro-macedonic acid methyl ester C31H46O4 ÏàËÆ¶È:64.5% Acta Pharmaceutica Sinica 1990 Vol 25 795-797 ISOLATION AND IDENTIFICATION OF YIBEINOSIDE A DM Xu; S Arihara; N Shoji; XW Yang; EX Huang and CS Li Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3¦Â,18¦Á,19¦Á)-ursane-3,20,28-triol C30H50O3 ÏàËÆ¶È:63.3% Helvetica Chimica Acta 2006 Vol. 89 3018 Three New Triterpenoids from Dracocephalum forrestii Gan-Peng Li, Jing-Feng Zhao, Li-Juan Yang , Xiao-Dong Yang, and Liang Li Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . aceriphyllic acid D C30H46O5 ÏàËÆ¶È:63.3% Journal of Natural Products 2009 72 1419-1423 Oleanane-Type Triterpenoids from Aceriphyllum rossii and Their Cytotoxic Activity Le Thi Kim Van, Tran Manh Hung, Phuong Thien Thuong, Tran Minh Ngoc, Jin Cheol Kim, Han-Su Jang,Xing Fu Cai,Sei Ryang Oh, Byung-Sun Min, Mi Hee Woo,Jae Sue Choi, Hyeong Kyu Lee, and KiHwan Bea Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . gamboukokoensein A C30H48O7 ÏàËÆ¶È:63.3% Phytochemistry 2003 845-849 Pentacyclic triterpenoid and saponins from Gambeya boukokoensis Jean Wandji, François Tillequin, Dulcie A. Mulholland, Jovita Chi Shirri,Nole Tsabang, ElisabethSeguin, Philippe Verite, Francine Libotb, Z.T. Fomum Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . cycloartan-23E-ene-1¦Á,2¦Á,3¦Â,25-tetrol C30H50O4 ÏàËÆ¶È:63.3% Journal of Natural Products 2008 71(1) 81-86 Cycloartane-Type Triterpenoids from the Resinous Exudates of Commiphora opobalsamum Tao Shen, Hui-Qing Yuan, Wen-Zhu Wan, Xiao-Ling Wang, Xiao-Ning Wang, Mei Ji, and Hong-Xiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 29,30-dibromoallobetulin C30H47O2Br2 ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 2006 42 186-188 SYNTHESIS AND CRYSTAL STRUCTURE OF 29,30-DIBROMOALLOBETULIN M. Yu. Lezhneva, E. E. Schultz I. Yu. Bagryanskaya,Yu. V. Gatilov, M. M. Shakirov,G. A. Tolstikov, and S. M. Adekenov Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 1 ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 1986 22 421-424 GLYCOSYLATION OF TRITERPENOIDS OF THE DAMMARANE SERIES. VI. 3-MONO- AND 3,12-DI-O-¦Â-D-GLUCOPYRANOSIDES OF PYXINOL L. N. Atopkina-and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 20(S),24(R)-epoxydammarane-3¦Â,12¦Â,25-triol ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 1982 18 546-571 CATALYTIC REARRANGEMENT OF 1,2 ORTHOACETATES OF ¦Á-D-GLUCOSE AND 20(S),24(R)-EPOXYDAMMARANE-3,123,25-TRIOLS. I. N. F. Samoshina, L. N. Atopkina, V. L. Novikov, V. A. Denisenko, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ursolic acid ÏàËÆ¶È:63.3% China Journal of Chinese Materia Medica 2003 28 527-531 Chemical Constituents from the Leaves of Dalbergia hainanensis ZHANG Peicheng, WU Yan, YU Dequan Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 19¦Á-hydroxyursolic acid ÏàËÆ¶È:63.3% China Journal of Chinese Materia Medica 1996 21 427-428 Studies on the Chemical Constituents of the Root of Boehmeira nivea (L.) Gaud Li Wenwu, Ding Liaheing and Li Bogang Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3¦Â,11¦Á-dihydroxytaraxer-14-en-12-one C32H52O5 ÏàËÆ¶È:63.3% Phytochemistry 2000 54 823-827 Two oleanane triterpenoids from Gordonia ceylanica and their conversions to taraxarane triterpenoids H.M.T.B. Herath, P.S. Athukoralage, Joanne F. Jamie Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 1¦Â,22¦Â-dihydroxyolean-11,13(18)-diene C30H48O2 ÏàËÆ¶È:63.3% Phytochemistry 1998 48 693-697 Saikosaponins from Taverniera aegyptiaca H. A. Hassanean Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3-epikatonic acid C30H48O3 ÏàËÆ¶È:63.3% Acta Pharmaceutica Sinica 1999 Vol 34 210-213 THE TRITERPENOIDS OF TRIPTERYGIUM WILFORDII Guo Fujiang (Guo FJ); Fang Peifen (Fang Pf) and Li Yuanchao (Li YC) Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Messaoenolide C30H48O4 ÏàËÆ¶È:63.3% Phytochemistry 1996 41 1573-1577 Triterpenoids from Melilotus messanensis; soyasapogenol G, the first natural carbonate derivative Francisco A. Mac¨ªas*, Ana M. Simonet, M. Dolores Esteban, Juan Carlos G. Galindo Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Neoalsooenin A ÏàËÆ¶È:63.3% Phytochemistry 1995 38 465-472 Dammarane glycosides from aerial parts of Neoalsomitra integrifoliola Seiji Fujita, Ryoji Kasai, Kazuhiro Ohtani, Kazuo Yamasaki, Ming-Hua Chiu, Rui-Lin Nie, Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 20(S)-protopanaxadiol oxide I ÏàËÆ¶È:63.3% Phytochemistry 1995 38 465-472 Dammarane glycosides from aerial parts of Neoalsomitra integrifoliola Seiji Fujita, Ryoji Kasai, Kazuhiro Ohtani, Kazuo Yamasaki, Ming-Hua Chiu, Rui-Lin Nie, Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Neoalsogenin G C30H50O4 ÏàËÆ¶È:63.3% Phytochemistry 1995 38 465-472 Dammarane glycosides from aerial parts of Neoalsomitra integrifoliola Seiji Fujita, Ryoji Kasai, Kazuhiro Ohtani, Kazuo Yamasaki, Ming-Hua Chiu, Rui-Lin Nie, Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . yunganogcnin F ÏàËÆ¶È:63.3% 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 25 . pomolic acid ÏàËÆ¶È:63.3% Phytochemistry 1992 31 1317-1320 Pomolic acid derivatives from the rootof Sanguisorba officinalis Cheng, D. and Cao, X. Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . yunganogenin F C30H46O5 ÏàËÆ¶È:63.3% Phytochemistry 1992 31 1747-1752 Oleanane glycosides from Glycyrrhiza yunnanensis roots Kazuhiro Ohtani, Katsuki Ogawa, Ryoji Kasai, Chong-Ren Yang, Kazuo Yamasaki, Jun Zhou, Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . neoalsogenin A C30H52O5 ÏàËÆ¶È:63.3% Phytochemistry 1992 31 2451-2453 A dammarane saponin from Neoalsomitra integrifoliola Hiromichi Nagasawa, Akira Isogai, Akinori Suzuki, Chiu Minghua, Nie Ruilin, Zhou Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (23R)-and (23S)-21,23-Epoxy-5¦Á-cycloart-24-en-3¦Â-ol C30H48O2 ÏàËÆ¶È:63.3% Phytochemistry 1992 31 4263-4274 Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei Hans Achenbach, Dieter Frey Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . compound 12 ÏàËÆ¶È:63.3% Phytochemistry 1992 31 4263-4274 Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei Hans Achenbach, Dieter Frey Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . Compound 10 ÏàËÆ¶È:63.3% Phytochemical Analysis 2009 20 320-327 Antioxidant diterpenoids from the roots of Salvia barrelieri Ufuk Kolak, Ahmed Kabouche, Mehmet Özt¨¹rk, Zahia Kabouche, G¨¹laçtl Topçu and Ayhan Ulubelen Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . Compound 1a ÏàËÆ¶È:63.3% Phytochemical Analysis 2009 20 320-327 Antioxidant diterpenoids from the roots of Salvia barrelieri Ufuk Kolak, Ahmed Kabouche, Mehmet Özt¨¹rk, Zahia Kabouche, G¨¹laçtl Topçu and Ayhan Ulubelen Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . maytenfolic acid C30H48O4 ÏàËÆ¶È:63.3% Phytochemistry 1986 25 479-485 Antitumour triterpenes of Maytenus diversifolia Hiroshi Nozaki, Hideyo Suzuki, Teruhisa Hirayama, Ryoji Kasai, Rong-Yang Wu, Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . ¦Á-amyrin ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2008 39 1296-1298 ¿íÒ¶Ý¡Â黯ѧ³É·ÖµÄÑо¿ ÖÜÔ¨;¼½±£È«;Íõì¿;ãÆÐ˹ú;Ê·ÀöÓ±;ÍõÓÀÆæ;·ë±¦Ãñ Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ÐܹûËá ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2008 39 499-502 ¿ÕÐÄÁ«×Ӳݻ¯Ñ§³É·ÖÑо¿ Âí׿;ÀîÇíÛë;·¶ÎÄǬ;·½Äî²®;ÁõìÍÎÄ Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . ursolic acid ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 1995 26 339-341+391 Studies on the Chemical Constituents of Indian Mockstrawberry(Duchesnea indica) Peng Jiangnan; Lu Yunru and Chen Dechang(Department of Materia Madica; Beijing college of Traditional Chinese; Beijing); Structure 13C NMR ̼Æ×Ä£Äâͼ |

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