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1 . lanosterol ÏàËÆ¶È:82.1% Phytochemistry 1984 23 1721-1723 23,24,25,26,27-Pentanorlanost-8-en-3¦Â,22-diol from Verticillium lecanii John Frederick Grove Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . trematenolic acid ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2002 50(12) 1603-1606 New Triterpenoids from Tricholoma saponaceum Kazuko YOSHIKAWA,Mina KUROBOSHI, Shigenobu ARIHARA,Naoko MIURA, Noriyuki TUJIMURA,and Kenji SAKAMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . trametenolic acid ÏàËÆ¶È:80% Journal of Natural Products 2005 68 69-73 Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2 Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . trametenolic acid ÏàËÆ¶È:80% Journal of Natural Products 1999 62 543-545 New Lanostanoid Glycosides from the Fruit Body of Laetiporus versisporus Kazuko Yoshikawa, Kenji Matsumoto, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . inotodiol ÏàËÆ¶È:80% Planta Medica 1986 52 495-496 3¦Â,22-Dihydroxylanosta-7,9(11),24-triene: A New, Minor Compound from Inonotus obliquus Kirsti Kahlos and R. Hiltunen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . inotodiol ÏàËÆ¶È:80% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . euphol ÏàËÆ¶È:80% Acta Pharmaceutica Sinica 1992 27 445-451 TRITERPENE CONSTITUENTS FROM EUPHORBIA NEMTOCYPHA HAND-MAZZ D Cao; YL Su; JS Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . lanosterol ÏàËÆ¶È:80% Acta Pharmaceutica Sinica 1996 31 524-529 STUDIES ON CHEMICAL CONSTITUENTS OF ROOTS OF EUPHORBIA PEKINENSIS LY Kong and ZD Min Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . euphol ÏàËÆ¶È:80% China Journal of Chinese Materia Medica 2005 30 1162-1165 Studies on chemical constitutes of green alga Chaetomorpha basiretorsa and their bioactivity Shi Dayong, HAN Lijun, SUN Jie, YANG Yongchun, SHI Jiangong, FAN Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . euphol C30H50O ÏàËÆ¶È:80% Phytochemistry 1999 50 849-857 (20R,23E)-Eupha-8,23-diene-3¦Â,25-diol from Tripetalum cymosum Yuan-Wah Leong, Leslie J. Harrison Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . lanosterol ÏàËÆ¶È:80% Phytochemistry 1999 50 849-857 (20R,23E)-Eupha-8,23-diene-3¦Â,25-diol from Tripetalum cymosum Yuan-Wah Leong, Leslie J. Harrison Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (23E)-lanosta-8,23-diene-3¦Â,25-diol ÏàËÆ¶È:80% Phytochemistry 1999 50 849-857 (20R,23E)-Eupha-8,23-diene-3¦Â,25-diol from Tripetalum cymosum Yuan-Wah Leong, Leslie J. Harrison Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . trametenolic acid B ÏàËÆ¶È:80% Phytochemistry 1996 41 1041-1046 Antimicrobial steroids from the fungus Fomitopsis pinicola Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . trametenolic acid C30H48O3 ÏàËÆ¶È:80% Phytochemistry 1993 32 1239-1244 Triterpenes of Poria cocos Takaaki Tai, Akira Akahori, Tetsuro Shingu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . euphol ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2010 41 877-881 ¸ÊË컯ѧ³É·ÖµÄÑо¿ ÎâÏþÀÚ;ÅËÇÚ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . euphol ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2008 39 1779-1781 Optimization of purification of Panax notoginseng extract for injection CHU Yang; SONG Hong-tao; LI Dan; YAN Lu; LIU Dan; CHEN Da-wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . tirucallol ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2008 39 1779-1781 Optimization of purification of Panax notoginseng extract for injection CHU Yang; SONG Hong-tao; LI Dan; YAN Lu; LIU Dan; CHEN Da-wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . lanosterol C30H50O ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2005 36 1763-1767 Ingenane diterpene ester constituents from Tibetan medicine Euphorbia wallichii LI Yu-lin; SUO You-rui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 3¦Â-dihydroxy-lanosta-8,24-diene-21-acid ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2001 32 4-6 Studies on chemical constituents of Fuscoporia obliqua HE Jian; FENG Xiao zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . lanosterol ÏàËÆ¶È:80% Journal of the Chemical Society, Perkin Transactions 1 1988 2403-2406 Penasterol, a novel antileukemic sterol from the okinawan marine sponge Penares sp. Jie-fei Cheng, Jun'ichi Kobayashi, Hideshi Nakamura, Yasushi Ohizumi, Yoshimasa Hirata and Takuma Sasaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . lanosterol ÏàËÆ¶È:80% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . inotodiol ÏàËÆ¶È:80% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . inotodiol ÏàËÆ¶È:80% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 24(E)-3¦Â-hydroxylanosta-8,24-dien-26-al-21-oic acid C30H46O4 ÏàËÆ¶È:80% The Journal of Antibiotics 2005 59 828-831 A New Cytotoxic Lanostane Triterpenoid from the Basidiomycete Hebeloma versipelle FREE Hong-Jun Shao, Chen Qing, Fei Wang, Yan-Li Zhang, Du-Qiang Luo and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . tirucallol ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2011 42 251-254 Chemical constituents of Omphalia lapidescens XU Ming-feng, SHEN Lian-qing, WANG Kui-wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . lanostadienol ÏàËÆ¶È:80% Organic Magnetic Resonance 1974 6 603-611 Carbon-13 NMR spectra of some tetra-and pentacyclic triterpenoids S. A. Knight Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . euphadienol ÏàËÆ¶È:80% Organic Magnetic Resonance 1974 6 603-611 Carbon-13 NMR spectra of some tetra-and pentacyclic triterpenoids S. A. Knight Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . Euphol C30H50O ÏàËÆ¶È:80% Molecules 2012 17 11826-11838 Inhibition of 11b-HSD1 by Tetracyclic Triterpenoids from Euphorbia kansui Jie Guo, Li-Yan Zhou, Hong-Ping He, Ying Leng, Zhen Yang and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . Euphol ÏàËÆ¶È:80% International Journal of Molecular Sciences 2012 13 11247-11259 Bio-Guided Isolation of the Cytotoxic Terpenoids from the Roots of Euphorbia kansui against Human Normal Cell Lines L-O2 and GES-1 Li Zhang, Lan Gao, Zhengjun Li, Xiaojing Yan, Yanjing Yang, Yuping Tang, Yudan Cao and Anwei Ding Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . Lanosterol ÏàËÆ¶È:78.5% Korean Journal of Pharmacognosy 2007 38(2) 164-169 Antioxidative Activities of Phenolic Compounds Isolated from Inonotus obliquus Kim, Hyoung-Ja; Jin, Chang-Bae; Lee, Yong-Sup Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . 15-deacetoxy-7,11-dihydroperenniporiol C30H48O3 ÏàËÆ¶È:78.5% Phytochemistry 1984 23 1129-1134 Determination of quassin in picogram quantities by an enzyme-linked immunosorbent assay R.J. Robins, M.R.A. Morgan, M.J.C. Rhodes, J.M. Furze Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . inonotsutriol A C30H50O3 ÏàËÆ¶È:76.6% Helvetica Chimica Acta 2008 Vol. 91 1513 Three New Lanostane Triterpenoids, Inonotsutriols A, B, and C, from Inonotus obliquus Sayaka Taji, Takeshi Yamada, and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . inonotsutriol B C30H50O3 ÏàËÆ¶È:76.6% Helvetica Chimica Acta 2008 Vol. 91 1513 Three New Lanostane Triterpenoids, Inonotsutriols A, B, and C, from Inonotus obliquus Sayaka Taji, Takeshi Yamada, and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . saponaceoic acid II C30H48O4 ÏàËÆ¶È:76.6% Chemical & Pharmaceutical Bulletin 2002 50(12) 1603-1606 New Triterpenoids from Tricholoma saponaceum Kazuko YOSHIKAWA,Mina KUROBOSHI, Shigenobu ARIHARA,Naoko MIURA, Noriyuki TUJIMURA,and Kenji SAKAMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . trametenolic acid ÏàËÆ¶È:76.6% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . euphol (eupha-8,24-di-en-3¦Â-ol) C30H50O ÏàËÆ¶È:76.6% China Journal of Chinese Materia Medica 2006 31 742-744 Studies on constituents from roots of Euphorbia hylonoma RUAN Hanli, ZHANG Yue, ZHANG Yonghui, PI Huifang, WU Jizhou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . trametenolic acid B ÏàËÆ¶È:76.6% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . compound 2 ÏàËÆ¶È:76.6% Phytochemistry 1991 30 3822-3823 A dammarane fromStevia salicifolia Rachel Mata, Vero´nica Rodri´guez, Rogelio Pereda-Miranda, Robert Bye, Edelmira Linares Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . Euphol ÏàËÆ¶È:76.6% Records of Natural Products 2012 6 255-262 Two New Phorbol-Type Diterpene Esters from Synadenium grantii Hook F. Leaves Emad M. Hassan, Magdy M. D. Mohammed and Samy M. Mohamed Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . euphol ÏàËÆ¶È:76.6% Phytochemistry 1990 29 1625-1628 Constituents of the latex of Euphorbia antiquorum Mohan B. Gewali,Masao Hattori,Yasuhiro Tezuka,Tohru Kikuchi,Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . compound II ÏàËÆ¶È:76.6% Phytochemistry 1984 23 2885-2888 Two perenniporiol derivatives, lanostane-type triterpenoids, from the cultured mycelia of Perenniporia ochroleuca Chieko Ino, Masao Hirotani, Tsutomu Furuya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . 15-deacetoxy-7,11-dihydroperenniporiol ÏàËÆ¶È:76.6% Phytochemistry 1984 23 2885-2888 Two perenniporiol derivatives, lanostane-type triterpenoids, from the cultured mycelia of Perenniporia ochroleuca Chieko Ino, Masao Hirotani, Tsutomu Furuya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . 3¦Â-21-dihydroxy-lanosta-8,24-diene ÏàËÆ¶È:76.6% Chinese Traditional and Herbal Drugs 2001 32 4-6 Studies on chemical constituents of Fuscoporia obliqua HE Jian; FENG Xiao zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . lanosterol ÏàËÆ¶È:76.6% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . trametenolicacid ÏàËÆ¶È:76.6% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ |
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