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PSA: ½ð±Ò+1, ÐÁ¿à 2013-01-16 12:50:51
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ÕâÊÇÄãÇóÖúµÄ»¯ºÏÎïÔÚÏàËÆ¶È60%ÒÔÉÏµÄÆ¥ÅäÐÅÏ¢ 1 . compoudn 2b ÏàËÆ¶È:94.7% Chemical & Pharmaceutical Bulletin 1990 38 1927-1930 The Constituents of Cistanche tubulosa (SCHRENK) HOOK. f. II. : Isolation and Structures of a New Phenylethanoid Glycoside and a New Neolignan Glycoside Fumio YOSHIZAWA,Takeshi DEYAMA,Nobuo TAKIZAWA,Khan USMANGHANI and Mansoor AHMAD Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . dehydrodiconiferyl alcohol ÏàËÆ¶È:94.7% Chemical & Pharmaceutical Bulletin 1987 35 1803-1807 The Constituents of Eucommia ulmoides OLIV. VI. Isolation of a New Sesquilignan and Neolignan Glycosides TAKESHI DEYAMA,TAKAKO IKAWA,SHIZUKA KITAGAWA and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . dehydrodiconiferylalcohol ÏàËÆ¶È:94.7% Journal of Natural Products 1992 Vol 55 214 The Structure of a New Neolignan Glycoside from Stauntonia chinensis Huai-Bin Wang, De-Quan Yu, Xiao-Tian Liang, Naoharu Watanabe, Masaharu Tamai, Sadafumi Omura Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . comopound 3b ÏàËÆ¶È:89.4% Chemical & Pharmaceutical Bulletin 1990 38 1927-1930 The Constituents of Cistanche tubulosa (SCHRENK) HOOK. f. II. : Isolation and Structures of a New Phenylethanoid Glycoside and a New Neolignan Glycoside Fumio YOSHIZAWA,Takeshi DEYAMA,Nobuo TAKIZAWA,Khan USMANGHANI and Mansoor AHMAD Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Spicatolignan B C20H20O7 ÏàËÆ¶È:75% Journal of Asian Natural Products Research 2007 9 445-449 Two new lignans from Mentha spicata L JIAN ZHENG, GUANG-TONG CHEN, HUI-YUAN GAO, BIN WU and LI-JUN WU Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . glycosmisic acid C20H20O7 ÏàËÆ¶È:75% Chinese Journal of Natural Medicines 2005 3 181-183 Chemical Constituents of Nauclea officinalis XUAN Wei-Dong; CHEN Hai-Sheng); YUAN Zhi-Xian; ZHU Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Glycosmisic acid ÏàËÆ¶È:75% Chinese Pharmaceutical Journal 2002 37 14-17 Study on chemical constituents isolated from Glycosmis citrifolia SHEN Xiao-Ling, ZENG Hui-Fang, CHEN Zhen, ZHONG Guang-Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . balanophonin C20H20O6 ÏàËÆ¶È:70% Journal of Shenyang Pharmaceutical University 2006 23 280-282 Chemical constituents of Nux Prinsepiae Uniflorae LI Hong-xuan, LI Xian, WANG Jin-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (7R,8S)-3,5'-dimethoxy-4',7-epoxy-8,3'-neolignane-5,9,9'-triol C20H24O6 ÏàËÆ¶È:70% Fitoterapia 2012 83 883-887 Phenolics from Leontopodium leontopodioides inhibiting nitric oxide production Xin Li, Jian-Guang Luo, Xiao-Bing Wang, Jun Luo, Jun-Song Wang, Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . balanophonin ÏàËÆ¶È:65% China Journal of Chinese Materia Medica 2009 34 1687-1689 Chemical constituents from Xanthium mongolicum ZHANGWenzhi, HAN Wei, LI Ying, ZHANG Shujun, ZHAO Defeng Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 4 ÏàËÆ¶È:65% Phytochemistry 1998 49 2125-2128 Revised structure for a neolignan from Brucea javanica Shiming Li, Knut Lundquist, Adrian F. A. Wallis Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 5 ÏàËÆ¶È:65% Phytochemistry 1998 49 2125-2128 Revised structure for a neolignan from Brucea javanica Shiming Li, Knut Lundquist, Adrian F. A. Wallis Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . epipinoresinol ÏàËÆ¶È:65% Phytochemistry 1990 29 1971-1980 Lignans of Forsythia intermedia Maiada M.A. Rahman,Paul M. Dewick,David E. Jackson,John A. Lucas Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 5-carboxy-6-(2-carboxy-4-hydroxy-5-methoxyphenyl)-8-hydroxy-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline C20H21NO8 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 15 . balanophonin ÏàËÆ¶È:65% Chinese Pharmaceutical Journal 2009 44 1133-1136 Study on Chemical Constituents from Bark of Fraxinus mandschurica Rupr. CHEN Yu-juan, WANG Hui-tang, HE Li-peng, ZHANG Hong-gui, YIN Jin-ling Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (-)-threo-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry 2012 20 4164-4171 Natural products as a gold mine for selective matrix metalloproteinases inhibitors Liyan Wang, Xi Li, Shoude Zhang, Weiqiang Lu, Sha Liao, Xiaofeng Liu, Lei Shan, Xu Shen, Hualiang Jiang, Weidong Zhang, Jin Huang, Honglin Li Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . lantibetin C2OH22O6 ÏàËÆ¶È:63.1% Planta Medica 2008 74 1391-1396 Minor Furofurano Lignans from the Tibetan Herb, Lancea tibetica Ting Li, Xiao-Jiang Hao, Qian-Qun Gu,Wei-Ming Zh Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . vibsanol C19H18O6 ÏàËÆ¶È:63.1% Chemical & Pharmaceutical Bulletin 1996 44 1418-1420 Two New Benzofuran-Type Lignans from the Wood of Viburnum awabuki Yoshiyasu FUKUYAMA,Mai NAKAHARA,Hiroyuki MINAMI and Mitsuaki KODAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (+)-1-hydroxy-2-epipinoresinol C20H22O7 ÏàËÆ¶È:63.1% Chemical & Pharmaceutical Bulletin 1985 33 1232-1241 Lignans from Bark of the Olea Plants. II HIROKI TSUKAMOTO,SUEO HISADA and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (+)-epipinoresinol C20H22O6 ÏàËÆ¶È:63.1% Chemical & Pharmaceutical Bulletin 1984 32 4653-4657 Effects of O-Methylation and O-Glucosylation on Carbon-13 Nuclear Magnetic Resonance Chemical Shifts of Matairesinol, (+)-Pinoresinol and (+)-Epipinoresinol SANSEI NISHIBE,HIROKI TSUKAMOTO and SUEO HISADA Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . vibsanol C19H18O6 ÏàËÆ¶È:63.1% Heterocycles 2000 52 643-659 An Expeditious Synthesis of Vibsanol, a Benzofuran-Type Lignan from Viburnum awabuki Atsushi Sakai, Toyohiko Aoyama,* and Takayuki Shioiri* Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (+)-1-hydroxy-pinoresinol ÏàËÆ¶È:63.1% Natural Product Research and Development 2006 18 772-774 Studies on Chemical Constituents of Periploca omeiensis ZHANG Yuan-hu; CHEN Dong-lin; WANG Feng-peng Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Ethyl 5-cyano-3-(4-fluorophenyl)-1-(4-nitrophenyl)-4-phenyl-2-pyrazoline-5-carboxylate C25H19FN4O4 ÏàËÆ¶È:63.1% Journal of the Brazilian Chemical Society 2009 20 975-987 Synthesis and Antimicrobial Evaluation of some New Pyrazole, Pyrazoline and Chromeno[3,4-c]pyrazole Derivatives Nada M. Abunada, Hamdi M. Hassaneen, Ahmed S. M. Abu Samaha and Omar A. Miqdad Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Ethyl 4-(4-chlorophenyl)-5-cyano-3-(4-fluorophenyl)-1-(4-nitrophenyl)-2-pyrazoline-5-carboxylate C25H18ClFN4O4 ÏàËÆ¶È:63.1% Journal of the Brazilian Chemical Society 2009 20 975-987 Synthesis and Antimicrobial Evaluation of some New Pyrazole, Pyrazoline and Chromeno[3,4-c]pyrazole Derivatives Nada M. Abunada, Hamdi M. Hassaneen, Ahmed S. M. Abu Samaha and Omar A. Miqdad Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . (+)-epipinoresinol ÏàËÆ¶È:63.1% Shoyakugaku Zasshi 1988 42 324-328 Phenolic Compounds from Forsythia Leaves (III) : On the Comparison of Constituents between Hybrid and Parents NISHIBE SANSEI, SAKUSHIMA AKIYO, KITAGAWA SHIZUKA, KLIMEK BARBARA, BENECKE RENATE, THIEME HEINZ Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . (-)-Tanegool-7'-methyl ether C21H26O7 ÏàËÆ¶È:61.9% Planta Medica 2012 78 480-484 Four New Cytotoxic Tetrahydrofuranoid Lignans from Sinopodophyllum emodi Yan-Jun Sun,Zhan-Lin Li,Hong Chen,Xiao-Qiu Liu,Wei Zhou,Hui-Ming Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . phillygenol ÏàËÆ¶È:60% Phytochemistry 1989 28 579-583 Farnesyl-homogentisic acid derivatives from Otoba parvifolia A.Gilberto Ferreira,Mario Motidome,Otto R. Gottlieb,João B. Fernandes,Paulo C. Vieira,Miriam Cojocaru,Hugo E. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ |
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