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²éѯ½á¹û£º¹²²éµ½528¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Á-Conidendrin C20H20O6 ÏàËÆ¶È:75% Acta Botanica Yunnanica 2004 26(2) 229-233 Lignans from Tsuga dumosa ZHAO You-Xing,LUO Xiao-Dong,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (-)-¦Á-conidendrin ÏàËÆ¶È:75% Natural Product Research and Development 2008 20 257-261 Chemical Constituents of Keteleeria evelyniana FU Zhao-hui;ZHANG Yu-mei; TAN Ning-hua; CHU Hong-biao; JI Chang-jiu; Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound -6 ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 1995 43 2200-2204 Pharmacologically Active Components of Todopon Puok (Fagraea racemosa), a Medicinal Plant from Borneo Emi OKUYAMA,Kuniharu SUZUMURA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Á-conidendrin C20H20O6 ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2000 31 246-248 Studies on Some Non-Taxane Constituents in Yunnan Yew (Taxus yunnanensis)Root Yunnan Academy of Forestry (Kunming )Xiang Wei Guizhou Institute of TCM Yao Ping Kunming Institute of Plant; Chinese Academy of Sciences Zhang Hongjie and Sun Handong Yunnan University Li Liang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . isolariciresinol ÏàËÆ¶È:70% Journal of Shenyang Pharmaceutical University 2003 20 101-103 Study on the chemical constituents of the fruits of Forsythia suspensa(Thunb.) Vahl LIU Yue, SONG Shao-jiang, XU Sui-xu, FU Xiao-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (+)-cycloolivil ÏàËÆ¶È:70% Chinese Chemical Letters 2011 22 85-87 A new aryltetrahydronaphthalene lignan from Epimedium brevicornum Hai Zhou Li, Guo Jun Luo, Hong Mei Li, Xiao Lei Li, Rong Tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (+)-carbonato de cicloolivil ÏàËÆ¶È:66.6% Qu¨ªmica Nova 2004 27 188-192 Lignans of Strychnos guianensis (Aublet) Mart. Pinheiro, Maria L¨²cia B.; Rocha, Arnaldo F. Imbiriba da; Fernandes, Marco A. do N.; Monte, Francisco Jos¨¦ Queiroz; Villar, Jos¨¦ Daniel Figueroa; Cruz, Elizabete Rangel Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6-Hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-hydroxymethyl-7-methoxy-3,4-dihydro-2-naphthaldehyde C20H20O6 ÏàËÆ¶È:65% Journal of Natural Products 2009 72 1627-1630 Nitric Oxide Scavenging Lignans from Vitex negundo Seeds Cheng-Jian Zheng, Bao-Kang Huang, Ting Han, Qiao-Yan Zhang,Hong Zhang, Khalid Rahman, and Lu-Ping Qin Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (¨C)-Isolariciresinol C20H24O6 ÏàËÆ¶È:65% Chemistry of Natural Compounds 2009 45 424-426 LIGNANS FROM Gnetum montanum Markgr. f. megalocarpua Li Qin Wang, You Xing Zhao,Lu Zhou and Jun Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . conidendrin ÏàËÆ¶È:65% Journal of Natural Products 1982 Vol 45 78-82 Lignans From Taxus wallichiana Roger W. Miller, Jerry L. McLaughlin, Richard G. Powell, Ronald D. Plattner, David Weisleder, Cecil R. Smith Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (+)-isolariciresinol ÏàËÆ¶È:65% Acta Pharmaceutica Sinica 2004 Vol 39 531-533 A new lignan glycoside from the flower of Castanea mollissima Blume TANG Wen-zhao; DING Xing-bao; XIN Yi-zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (+)-isolariciresinol C20H24O6 ÏàËÆ¶È:65% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 8 1028-1031 Study on chemical constituents from leaves of Tripterygium wilfordii CAO Xu, LI Chuang jun, YANG Jing zhi, WEI Baixing, LUO Yongming, ZHANG Dongming Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 8-(4-hydroxy-2-hydroxymethyl-5-methoxyphenyl)-6-hydroxy-7-methoxy-N-methyl-1,2,3,4-tetrahydroisoquinoline C19H23NO5 ÏàËÆ¶È:65% Heterocycles 2003 60 1573-1588 Preparation of 6-Phenyl- and 8-Phenyl Tetrahydro-isoquinolines from Boldine Wei-Jan Huang, Chung-Hsiung Chen, and Shoei-Sheng Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-hydroxymethyl-7-methoxy-3,4-dihydro-2-naphthaldehyde ÏàËÆ¶È:65% Journal of Natural Medicines 2008 62 47-51 Two new lignan glucosides from the fruit of Vitex cannabifolia Toru Yamasaki, Tetsuro Kawabata, Chikako Masuoka, Junei Kinjo and Tsuyoshi Ikeda, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Isolariciresinol C17H26O10 ÏàËÆ¶È:65% Chemistry of Natural Compounds 2010 46 459-461 Chemical investigation of Ervatamia yunnanensis Jing-Ling Du, Yong-Sheng Jin, Li-Ming Qiao, Li Jin and Hai-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (+)-isolariciresinol ÏàËÆ¶È:65% Journal of Shenyang Pharmaceutical University 2010 27 116-119 Isolation and identification of chemical constituents from bulk of Pinellia ternata XU Jian-kun, ZHANG Tian-long, YI Guo-qing, XU Ying, WU Hong-hua, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (+)-isolariciresinol C20H24O6 ÏàËÆ¶È:65% |
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