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yteamoy: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ºÜºÃ£¬ºÜ¸øÁ¦£¡Ð»Ð»£¡ 2012-10-19 17:15:42
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yteamoy: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ºÜºÃ£¬ºÜ¸øÁ¦£¡Ð»Ð»£¡ 2012-10-19 17:15:42
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²éѯ½á¹û£º¹²²éµ½4590¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Soyasapogenol E ÏàËÆ¶È:76.6% Phytochemistry 1998 49 709-717 Bioactive polar triterpenoids from Melilotus messanensis Francisco A. Mac¨ªas, Ana M. Simonet, Juan Carlos G. Galindo, Pedro C. Pacheco, Jose A. S¨¢nchez Structure 13C NMR̼Æ×Ä£Äâͼ 2 . olean-18-en-3-one ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 2002 50(9) 1273-1275 Fern Constituents: Triterpenoids from Adiantum capillus-veneris Takahisa NAKANE,Yoshiko MAEDA, Hideharu EBIHARA,Yoko ARAI,Kazuo MASUDA,Akihito TAKANO, Hiroyuki AGETA,Kenji SHIOJIMA,Shao-Qing CAI,and Osama Bashir ABDEL-HALIM Structure 13C NMR̼Æ×Ä£Äâͼ 3 . Abrisapogenol F ÏàËÆ¶È:73.3% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR̼Æ×Ä£Äâͼ 4 . soyasapogenol E ÏàËÆ¶È:73.3% Journal of Natural Products 1988 Vol 51 335 Melilotigenin, a New Sapogenin from Melilotus officinalis Sam Sik Kang, Won Sick Woo Structure 13C NMR̼Æ×Ä£Äâͼ 5 . soyasapogenol E ÏàËÆ¶È:73.3% Journal of Natural Products 1991 Vol 54 830 Constituents of Leguminous Plants, XIII. New Triterpenoid Saponins from Wistaria brachybotrys Takao Konoshima, Mutsuo Kozuka, Mitsumasa Haruna, Kazuo Ito Structure 13C NMR̼Æ×Ä£Äâͼ 6 . Soyasapogenol E ÏàËÆ¶È:73.3% Korean Journal of Pharmacognosy 2008 39(3) 186-193 Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik Structure 13C NMR̼Æ×Ä£Äâͼ 7 . camelliagenone C30H48O4 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 2011 59(6) 778-782 New Triterpenes from Barringtonia asiatica Consolacion Yasa㸠RAGASA, Dinah Lorenzana ESPINELI, and Chien-Chang SHEN Structure 13C NMR̼Æ×Ä£Äâͼ 8 . ¦Â-amyrenone C30H48O ÏàËÆ¶È:73.3% 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 NMR̼Æ×Ä£Äâͼ 9 . ¦Â-amyrone ÏàËÆ¶È:73.3% Chinese Journal of Natural Medicines 2010 8 244-246 A New Benzoic Acid Derivative from Eclipta prostrata SUN Zhi-Hua; ZHANG Chao-Feng; ZHANG Mian Structure 13C NMR̼Æ×Ä£Äâͼ 10 . 21¦Â,28-dihydroxy-3-oxo-olean-12,20(30)-diene C29H44O3 ÏàËÆ¶È:72.4% Tetrahedron 2001 57 8413-8424 Immunosuppressive terpenoids from extracts of Tripterygium wilfordii Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto, Takao Taki, Motoo Tori, Shigeru Takaoka, Yongfeng Jia, Duan Li Structure 13C NMR̼Æ×Ä£Äâͼ 11 . 29-hydroxy-12-oleanene-3,22-dione C30H46O3 ÏàËÆ¶È:70% 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 NMR̼Æ×Ä£Äâͼ 12 . sumaresinolic acid ÏàËÆ¶È:70% Journal of Natural Products 2006 69(5) 807-810 Triterpenoids from the Resin of Styrax tonkinensis and Their Antiproliferative and Differentiation Effects in Human Leukemia HL-60 Cells Feng Wang, Huiming Hua, Yuehu Pei, Duo Chen, and Yongkui Jing Structure 13C NMR̼Æ×Ä£Äâͼ 13 . abrisapogenol F C30H48O2 ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 1989 37 846-848 NEW TRITERPENOID SAPOGENOLS FROM ABRUS CANTONIENSIS (I) Takashi TAKESHITA,Shuichi HAMADA and Toshihiro NOHARA Structure 13C NMR̼Æ×Ä£Äâͼ 14 . ¦Â-amyrone ÏàËÆ¶È:70% Acta Botanica Sinica 2001 43 426-430 The Chemical Constituents of Amoora yunnanensis LUO Xiao-Dong, WU Shao-Hua, MA Yun-Bao, WU Da-Gang Structure 13C NMR̼Æ×Ä£Äâͼ 15 . ST-F 1 ÏàËÆ¶È:67.7% Chemistry of Natural Compounds 1997 33 316-319 TRITERPENE GLYCOSIDES OF Hedera taurica XVI. STRUCTURES OF GLYCOSIDES St-A, St-B 1, St-B 2, St-C,St-D1, St-D2, St-E, St-F 1, AND St-F 2 FROM THE STEMS OF CRIMEAN IVY V. I. GriShkovets, S. V. Godin, O. Ya. Tsvetkov,A. S. Shamhkov, and V. Ya. Chirva Structure 13C NMR̼Æ×Ä£Äâͼ 16 . methyl 3-epi-sumaresinolate C31H50O4 ÏàËÆ¶È:67.7% 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 NMR̼Æ×Ä£Äâͼ 17 . 3-Oxo-12-en-28-(2'-nitro-vinyl)-olean C31H47NO3 ÏàËÆ¶È:67.7% Journal of Asian Natural Products Research 2012 14 355-363 Synthesis and biological evaluation of oleanolic acid derivatives as antitumor agents Lei Chen,Jian-Bo Wu,Fan Lei,Shan Qian,Li Hai and Yong Wu Structure 13C NMR̼Æ×Ä£Äâͼ 18 . 2,3-seco-3-oxoolean-12-en-2-oic acid C30H48O3 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2003 51(1) 89-91 New Triterpenoids from Gentiana lutea Yoshitaka TORIUMI, Rie KAKUDA, Masafumi KIKUCHI, Yasunori YAOITA, and Masao KIKUCHI Structure 13C NMR̼Æ×Ä£Äâͼ 19 . 3¦Á,21¦Â-dihydroxy-olean-12-ene 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-R |
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