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xiaoxiao270: ½ð±Ò+4 2013-02-25 19:42:05
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²éѯ½á¹û£º¹²²éµ½6445¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . salaspermic acid methyl ester ÏàËÆ¶È:87.0% Journal of Natural Products 1994 Vol 57 1 Quinone-Methide Triterpenes and Salaspermic Acid from Kokoona ochracea Olipa Ngassapa, Djaja D. Soejarto, John M. Pezzuto, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . salaspermic acid ÏàËÆ¶È:83.3% Journal of Natural Products 1994 Vol 57 1 Quinone-Methide Triterpenes and Salaspermic Acid from Kokoona ochracea Olipa Ngassapa, Djaja D. Soejarto, John M. Pezzuto, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2¦Á-acetoxy-3¦Â,24-epoxy-3¦Á-hydroxy-D:A-friedooleanan-29-oicacid methyl ester C33H52O6 ÏàËÆ¶È:83.3% Phytochemistry 2012 84 116-124 Studies of naturally occurring friedelane triterpenoids as insulin sensitizers in the treatment type 2 diabetes mellitus Alejandro E. Ardiles, ¨¢gueda Gonz¨¢lez-Rodr¨ªguez, Marvin J. N¨²ñez, Nayra R. Perestelo, Virginia Pardo, Ignacio A. Jim¨¦nez, ¨¢ngela M. Valverde, Isabel L. Bazzocchi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . friedelan-3¦Â-ol ÏàËÆ¶È:76.6% Natural Product Research and Development 2001 13(1) 14-16 STUDY ON THE CHEMICAL CONSTITUENTS OF ASPIDOPTERYS OBCORDATA HEMSL. WU Rui; YE Qi; CHEN Neng yu; ZHANG Guo lin Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Â,24-epoxy-2a,3¦Á-dihydroxy-D:A-friedooleanan-29-oic acidmethyl ester C31H50O5 ÏàËÆ¶È:76.6% Phytochemistry 2012 84 116-124 Studies of naturally occurring friedelane triterpenoids as insulin sensitizers in the treatment type 2 diabetes mellitus Alejandro E. Ardiles, ¨¢gueda Gonz¨¢lez-Rodr¨ªguez, Marvin J. N¨²ñez, Nayra R. Perestelo, Virginia Pardo, Ignacio A. Jim¨¦nez, ¨¢ngela M. Valverde, Isabel L. Bazzocchi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 4¦Á-Hydroxyfriedel-3-one C30H50O2 ÏàËÆ¶È:73.3% Journal of Natural Products 2004 67 1193-1196 Hemisynthetic Secofriedelane Triterpenes with Inhibitory Activity against the Growth of Human Tumor Cell Lines in Vitro Cristina Moiteiro, Csar Manta, Ftima Justino, Regina Tavares, Maria Joo M. Curto, Madalena Pedro, Maria So Jos Nascimento, and Madalena Pinto Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . mudanpinoic acid A C30H46O3 ÏàËÆ¶È:73.3% Journal of Natural Products 1998 61 343-346 Two Novel Compounds from Paeonia suffruticosa Hang-Ching Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . epifriedlinol ÏàËÆ¶È:73.3% China Journal of Chinese Materia Medica 1997 22 103-104 Studies on the Chemical Constituents of Aster poliothamnus Diels Zhang Jiamin and Chen Yaozu, Li Bogang and Wang Mingkui Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . orthosphenic acid ÏàËÆ¶È:73.3% 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 10 . epifricdelinol ÏàËÆ¶È:73.3% Journal of Shenyang Pharmaceutical University 1999 16 194-197 A Study on the Chemical Constituents of Quercus engleriana Seem. Zhou Yingjun, Sun Qishi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . friedelan-3¦Â-ol ÏàËÆ¶È:73.3% Journal of Ethnopharmacology 2000 72 465-468 Evaluation of the antiulcerogenic activity of friedelan-3¦Â-ol and friedelin isolated from Maytenus ilicifolia (Celastraceae) Carmen Lucia Queiroga, Guilherme Faria Silva, Patrı́cia Corr¨ºa Dias, Ana Possenti, João Ernesto de Carvalho Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . epifriedelinol ÏàËÆ¶È:72.4% Korean Journal of Pharmacognosy 2007 38(1) 67-70 Isolation of Isoprenoidal Compounds from the Stems of Acer tegmentosum Max Hur, Jong-Moon; Jun, Mi-Ra; Yang, Eun-Ju; Choi, Sun-Ha; Park, Jong-Cheol; Song, Kyung-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (2¦Á,3¦Â,4¦Â,5¦Â,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,24R)-3,24-Epoxy-24-ethoxy-2,24-dihydroxy-5,9,13-trimethyl-24,25,26-trinoroleanan-29-oic Acid2) ÏàËÆ¶È:70% Helvetica Chimica Acta 2000 Vol. 83 3344 Chemical Constituents of Tripterygium wilfordii Guangzhong Yang, Xueqiang Yin, and Yuanchao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . punicanolic acid C30H50O4 ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 2008 56(11) 1628-1631 Medicinal Flowers. XXIII.1) New Taraxastane-Type Triterpene,Punicanolic Acid, with Tumor Necrosis Factor-a Inhibitory Activity from the Flowers of Punica granatum Yuanyuan XIE,Toshio MORIKAWA,Kiyofumi NINOMIYA,Katsuya IMURA,Osamu MURAOKA,Dan YUAN,and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 26-hydroxy-1,3-friedelanedione ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 1999 47 1725-1729 Antidiabetic Principles of Natural Medicines. IV. Aldose Reductase and ¦Á-Glucosidase Inhibitors from the Roots of Salacia oblonga WALL. (Celastraceae) : Structure of a New Friedelane-Type Triterpene, Kotalagenin 17-Acetate Hisashi MATSUDA,Toshiyuki MURAKAMI,Kenichi YASHIRO,Johji YAMAHARA and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . wilforic acid E ÏàËÆ¶È:70% 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 17 . glutinol ÏàËÆ¶È:70% Natural Product Sciences 2004 10 306-309 Triterpenoids from Orostachys japonicus Lee, Sang-Hyun; Paek, Sun-Ha; Kim, Seung-Ki; Kim, Bak-Kwang; Shin, Kuk-Hyun Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . trichadenic acid B ÏàËÆ¶È:70% 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 19 . compound 182 ÏàËÆ¶È:70% 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 . compound 191 ÏàËÆ¶È:70% 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 . trichadenic acid B ÏàËÆ¶È:70% Phytochemistry 1992 31 223-225 30-Norfriedelane triterpenes from the stem bark ofCaloncoba glauca Rosa M. Giner-Pons, Alexander I. Gray, Catherine Lavaud, Georges Massiot, Simon Gibbons, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ |
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