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²éѯ½á¹û£º¹²²éµ½2766¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 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 2 . ursolic acid ÏàËÆ¶È:66.6% 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 3 . euscaphic acid ÏàËÆ¶È:66.6% Pharmazie 2008 63 765-767 Euscaphic acid, a new hypoglycemic natural product from Folium Eriobotryae Jian Chen, Wei-Lin Li, Ju-Lan Wu, Bing-Ru Ren and Han-Qing Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . euscaphic acid ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2005 40 1052-1054 Study on chemical constituents of Potentilla discolor XLE Pei-feng, YIN Ting, LIANG Hong, ZHAO Yu-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . euscaphic acid ÏàËÆ¶È:66.6% Journal of Peking University (Health Sciences) 2004 36 21-23 Studies on the chemical constituents from Potentilla multifida L. XUE Pei feng; QIAO Liang; LIANG Hong; ZHAO Yu ying Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2¦Á,3¦Á,19¦Á-ÈýôÇ»ù-12 Ï©-28-ÎÚËÕËá ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2011 42 2200-2203 Chemical constituents in Potentilla kleiniana LI, Sheng-hua, WU, Xian-jin, NIU, You-ya, ZENG, Jun-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Larreagenin A ÏàËÆ¶È:65.5% Planta Medica 1989 55 303-306 Yemuoside YM7, YM11, YM13, and YM14:Four Nortriterpenoid Saponins from Stauntonia chinensis Huai-Bin Wang,De-Quan Yu,Xiao-Tian Liang, Naoharu Watanabe, Masaharu Tamai, and Sadafumi Omura Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 30-nor,larreagenin A ÏàËÆ¶È:65.5% 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 9 . (22R)-methylcholest-5-en-3¦Â,22,28-tetraol-3,22,28-triacetate ÏàËÆ¶È:65.5% Chinese Journal of Chemistry 2001 19 515-517 Sardisterol, A New Polyhydroxylated Sterol from the Soft Coral Sarcophyton digitatum Moser Jing-Yu Su, Ruo-Lin Yang and Long-Mei Zeng Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . methyl pomolate ÏàËÆ¶È:64.5% Chemical & Pharmaceutical Bulletin 1987 35 841-845 Two New Triterpenoid Glycosides from Leaves of Ilex chinensis SIMS AKIRA INADA,MARI KOBAYASHI,HIROKO MURATA and TSUTOMU NAKANISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ilexpernoside J C48H78O20 ÏàËÆ¶È:63.3% Helvetica Chimica Acta 2008 Vol. 91 1630 Triterpene Saponins from the Leaves of Ilex pernyi Guang-Bo Xie, Jiao Zheng, Peng-Fei Tu, and Guo-Qing Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â-hydroxy-12-oxo-13H¦Á-olean-28,19¦Â-olide C30H46O4 ÏàËÆ¶È:63.3% 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 NMR ̼Æ×Ä£Äâͼ 13 . compound 9 ÏàËÆ¶È:63.3% Journal of Natural Products 1996 59 304-307 Triterpenoids from Adina rubella Shi-yue Fang, Zhi-sheng He, and Gao-jun Fan, Hou-ming Wu and Jing-fei Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . pomolic acid C36H46O4 ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 1992 40 1990-1992 Triterpenoid Saponins of Aquifoliaceous Plants. V. Ilexosides XV-XIX from the Barks of Ilex crenata THUNB. Chieko HATA,Miho KAKUNO,Kazuko YOSHIKAWA and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . pomolic acid C30H48O4 ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 1992 40 3138-3141 Triterpenoid Saponins of Aquifoliaceous Plants. VIII. Ilexosides XXIX-XXXII from the Leaves of Ilex rotunda THUNB. Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 20(S),24(R)-epoxydammarane-3¦Â,11¦Â,25-triol ÏàËÆ¶È:63.3% Chemistry of Natural Compounds 1980 16 40-43 REFINEMENT OF THE STBUCTUBES OF TBITEB PENES FEOM THE LEAVES OF Betula ermanii V. L. Novikov, G. V, Malino vskaya, N. D. Pokhilo, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3¦Â,19-dihydroxyolean-12-en-28-oic acid C30H48O4 ÏàËÆ¶È:63.3% Acta Botanica Boreali-Occidentalia Sinica 2007 27 1141-1146 The Triterpenes in Salvia umbratica LIU Qing, LIU Zhen-ling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . glyyunnansapogenin B2 ÏàËÆ¶È:63.3% Acta Pharmaceutica Sinica 1995 30 27-33 NEW TRTEKPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS JF Hu; ZL Ye and FJ Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound S ÏàËÆ¶È:63.3% Journal of Asian Natural Products Research 2005 7 829-834 Two new triterpenoid saponins from Sarcandra glab Y.-M. LUO, A.-H. LIU, D.-M. ZHANG and L.-Q. HUANG Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 2¦Á,3¦Á,19¦Á,23-Tetrahydroxyurs-12-en-28-oic Acid ÏàËÆ¶È:63.3% Journal of Asian Natural Products Research 2003 5 49-56 BIOACTIVE TRITERPENOIDS FROM SYMPLOCOS CHINENSIS XI-HAO LI, DIAN-DIAN SHEN, NAN LI and SHI-SHAN YU Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . euscaphic acid ÏàËÆ¶È:63.3% Natural Product Research 2008 22 1310-1316 Two new 11¦Á,12¦Á-epoxy-ursan-28,13¦Â-olides and other triterpenes from Cecropia catharinensis E. C. Machado; R. A. Yunes; A. Malheiros; E. C. Gomez; F. Delle Monache Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . pomolic acid ÏàËÆ¶È:63.3% China Journal of Chinese Materia Medica 2005 30 1833-1836 Triterpenes from root of Rhaponticum uniflorum ZHANG Yonghong, ZHANG Jiangang, XIE Jieming, CHEN Gelin, CHENG Dongliang Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Euscaphic acid C30H48O5 ÏàËÆ¶È:63.3% Journal of Natural Products 1989 Vol 52 162 Pentacyclic Triterpenes from the Fruits of Rosa sterilis Liang Guang-Yi, Alexander I. Gray, Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . alamosenogenin C30H48O4 ÏàËÆ¶È:63.3% Journal of Natural Products 1995 Vol 58 1913-1914 A New Triterpene from Rathbunia alamosensis Takaomi Takizawa, Kaoru Kinoshita, Kiyotaka Koyama, Kunio Takahashi, Norio Kondo, Hiroshi Yuasa Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 34 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 26 . pomolic acid 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 27 . compound 232 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 28 . 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 29 . pomolic acid C30H48O4 ÏàËÆ¶È:63.3% Phytochemistry 1992 31 2809-2812 Triterpene saponins from fruit of Ilex crenata Takashi Kakuno, Kazuko Yoshikawa, Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . pomolic acid C30H46O4 ÏàËÆ¶È:63.3% Phytochemistry 1992 31 3553-3557 Saturated hopane and gammacerane triterpene-diols from the stem bark of Abies veitchii Reiko Tanaka, Shunyo Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . euscaphic acid ÏàËÆ¶È:63.3% Journal of Natural Products 2010 73 1655-1658 Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica Jing-Jy Cheng, Li-Jie Zhang, Hui-Ling Cheng, Chun-Tang Chiou, I-Jung Lee, and Yao-Haur Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . rotungenic acid C30H48O5 ÏàËÆ¶È:63.3% Phytochemistry 1989 28 1479-1482 Triterpenes from Ilex rotunda fruits Munehiro Nakatani,Yuji Miyazaki,Takashi Iwashita,Hideo Naoki,Tsunao Hase Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 3¦Â,22¦Â-dihydroxy-olean-12-en-29-oic acid (22-epi-maytenfolic acid) C30H48O4 ÏàËÆ¶È:63.3% Magnetic Resonance in Chemistry 2002 40 366-370 Epikatonic acid from Austroplenckia populnea: structure elucidation by 2D NMR spectroscopy and X-ray crystallography G. D. F. Silva, L. P. Duarte, S. A. Vieira Filho, A. C. Doriguetto, Y. P. Mascarenhas, J. Ellena, E. E. Castellano and A. B. Cota Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 19¦Á-ôÇ»ùÎÚËÕËá ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2009 40 369-371 ×϶¡ÏãÒ¶»¯Ñ§³É·ÖÑо¿ ÀîÈ«;ÐíÇíÃ÷;ºÂÀöÀò;½±ù·Ò;ÑîÊÀÁÖ;ÀîЦȻ Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . rotungenic acid C30H46O5 ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2009 40 1036-1039 ŵÀöÇà¹û»¯Ñ§³É·ÖÑо¿ ÌÀ½¨¹ú;Èθ£²Å;Áõ¼ª¿ª Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . pomolic acid ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2006 37 1632-1633 èÁèËÒ¶µÄ»¯Ñ§³É·ÖÑо¿(¢ñ) ³Â½£;ÀîάÁÖ;Îâ¾ÕÀ¼;ÕźÇì Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 6¦Â,19¦Á-dihydroxy ursolic acid C30H48O5 ÏàËÆ¶È:63.3% Chinese Journal of Natural Medicines 2007 5 413-416 Chemical Constituents from Hypericum ascyron GAO Ying; HAN Li; SUN Liang; ZHENG Dan; HUANG Xue-Shi; YU Shi-Shan Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . euscaphic acid C30H48O5 ÏàËÆ¶È:63.3% Chinese Journal of Natural Medicines 2010 8 12-15 Triterpenoids from the Roots of Rose odorata var.gigantean LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . euscaphic acid ÏàËÆ¶È:63.3% Journal of China Pharmaceutical University 2002 33 184-187 Studies on the Constituents of Rosa multiflora Thunb LI Yan Fang*; HU Li Hong; LOU Feng Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . pomolic acid C30H48O4 ÏàËÆ¶È:63.3% Natural Product Research and Development 2001 13(2) 11-13 THE STUDIES OF CHEMICAL COMPONENTS OF CLAUSENA DUNNIANA CUI Shu ya;CHENG Dong liang; TIAN Jun; WU Feng e Structure 13C NMR ̼Æ×Ä£Äâͼ |

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