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»¯ºÏÎï1 22.0,22.4,26.0,27.9,37.2,42.3,53.0,53.4,53.7,55.6,59.2,71.6,110.5,111.9,119.2,119.8,122.4,137.8,138.8 »¯ºÏÎï2 55.1,55.6,56.3,56.4,56.8,61.8,72.4,72.8,74.1,86.8,86.9,88.4,104.6,111.5,112.1,116.5,116.9,120.2,121.0,133.5,138.6,147.7,148.4,148.9,149.3,154.5 »¯ºÏÎï3 56.2,56.4,56.5,56.9,65.1,87.6,112.5,114.5,115.6,115.8,121.7,122.8,132.8,132.8,146.2,147.0,148.5,148.7 |
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»¯ºÏÎï1 1 . Coronaridine ÏàËÆ¶È:68.4% Phytochemistry 1980 19 1213-1218 Anticancer indole alkaloids of Ervatamia heyneana Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 19R-epi-heyneanine ÏàËÆ¶È:66.6% Planta Medica 1983 49 148-150 Tertiary Indole Alkaloids from Leaves of Tabernaemontana dichotoma Premila Perera, Gunnar Samuelsson, Tens A. van Beek and Robert Verpoorte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 19-isoheyneanine ÏàËÆ¶È:66.6% Helvetica Chimica Acta 1976 59 2437-2442 13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 19S-Heyneanine ÏàËÆ¶È:65% Phytochemistry 1980 19 1213-1218 Anticancer indole alkaloids of Ervatamia heyneana Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 19-epi-heyneanine ÏàËÆ¶È:61.9% China Journal of Chinese Materia Medica 2007 32 1296-1299 Study on chemical constituents in rhigome of Ervatamia hainanensis LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 19-R-hyyneanine ÏàËÆ¶È:61.9% Natural Product Sciences 1997 3 42-48 Alkaloids from The Roots of Tabernaemontana Macrocarpa Jack Husain, Khairana; Said, Ikram M.; Din, Laily B.; Takayama, Hiromitsu; Kitajima, Mariko; Aimi, Norio Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . heyneanine ÏàËÆ¶È:61.9% Helvetica Chimica Acta 1976 59 2437-2442 13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 19,20-dihydrousambarensine C29H30N4 ÏàËÆ¶È:60% Phytochemistry 1992 31 2873-2876 Alkaloids from roots of Strychnos potatorum Georges Massiot, Philippe Thepenier, Marie-Jos¨¦ Jacquier, Louisette Le Men-Olivier, Cl¨¦ment Delaude Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . N-Boc-L-Trp-L-Leu methyl ester C23H33N3O5 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2012 20 2002-2009 Cyclic dipeptides exhibit potency for scavenging radicals Tadashi Furukawa, Takashi Akutagawa, Hitomi Funatani, Toshikazu Uchida, Yoshihiro Hotta, Masatake Niwa, Yoshiaki Takaya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 19-epi-isovoacristine C22H28N2O4 ÏàËÆ¶È:59.0% Journal of Natural Products 2002 65 669-672 Five New Iboga Alkaloids from Tabernaemontana corymbosa Toh-Seok Kam and Kooi-Mow Sim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 19-epi-isovoacristine C22H28N2O4 ÏàËÆ¶È:59.0% Chemical & Pharmaceutical Bulletin 1994 42 280-284 Two New Dimeric Indole Alkaloids from Tabernaemontana subglobosa MERR. from Taiwan Hiromitsu TAKAYAMA,Shinya SUDA,Ih-Sheng CHEN,Mariko KITAJIMA,Norio AIMI and Shin-ichiro SAKAI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (-)-3R-Methoxycoronaridine ÏàËÆ¶È:59.0% Phytochemistry 1994 37 1729-1735 Indole alkaloids and terpenoids fromTabernaemontana markgrafiana Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . ervayunine C19H24N2O ÏàËÆ¶È:57.8% Planta Medica 1988 54 519-521 Ervayunine: A New Indole Alkaloid from Ervatamia yunnanensis Liu Gui, Liu Xint, and Feng Xiao-zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . voaphylline ÏàËÆ¶È:57.8% Planta Medica 1988 54 519-521 Ervayunine: A New Indole Alkaloid from Ervatamia yunnanensis Liu Gui, Liu Xint, and Feng Xiao-zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . trans-1,12¦Â octahydro-1,2,3,4,6,7,12,12¦Â-methanooxymethanol-1,12-indolo 2,3¦Á quinolizine ÏàËÆ¶È:57.8% Journal of Natural Products 1985 Vol 48 273-278 Partial Synthesis via Indole Alkaloids: A New Hexacyclic Derivative of (-)-Tetrahydroalstonine Bernhard Mompon, Thierry Vassal, Philippe Poirier Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . cleavamine ÏàËÆ¶È:57.8% Helvetica Chimica Acta 1976 59 2711-2723 13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . koumidine ÏàËÆ¶È:57.8% Phytochemistry 1987 26 2875-2876 Revision of the stereochemistry of koumidine Yeh Schun,Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 4,5-seco-neopulchell-5-ene-2-O-acetate ÏàËÆ¶È:57.8% Phytochemistry 1988 27 2887-2891 Sesquiterpene lactones from Gaillardia pulchella Sanggong Yu,Nianbai Fang,Tom J. Mabry,Khalil A. Abboud,Stanley H. Simonsen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . N-desacetyl retuline ÏàËÆ¶È:57.8% Phytochemistry 1988 27 3293-3304 Alkaloids from roots of Strychnos matopensis Georges Massiot,Bernard Massoussa,Marie-Jos¨¦ Jacquier,Philippe Th¨¦p¨¦nier,Louisette Le Men-Olivier,Cl¨¦ment Delaude,Robert Verpoorte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 1 C19H22N2O ÏàËÆ¶È:57.8% Tetrahedron Letters 2003 44 8013-8017 The first enantiospecific synthesis of (?)-koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction. The stereospecific introduction of the 19-(Z) ethylidene side chain Hui Cao, Jianming Yu, Xiangyu Z. Wearing, Chunchun Zhang, Xiaoxiang Liu, Jeffery Deschamps, James M. Cook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound 9c ÏàËÆ¶È:57.8% Tetrahedron Letters 2005 46 3037-3040 Design and synthesis of novel oxa-bridged isoxazolidines and 1,3-aminoalcohols Krishna P. Kaliappan, Prasanta Das, Nirmal Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (¡À)-18-noraspidospermidine C18H24N2 ÏàËÆ¶È:57.8% Tetrahedron 1999 55 11095-11108 Synthesis of aspidospermidine alkaloids from 1,2,3,4-tetrahydrocarbazole: Total stereoselective synthesis of (¡À)-18-noraspidospermidine Anah¨ª Urrutia, J.Gonzalo Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 19-Heyneanine C21H26N2O3 ÏàËÆ¶È:57.1% Chemistry of Natural Compounds 2008 44 675-678 INDOLE ALKALOIDS FROM Ervatamia flabellformia Shuang Liang, Haisheng Chen, Li Jin,Weidong Xuan, and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 19-heyneanine ÏàËÆ¶È:57.1% China Journal of Chinese Materia Medica 2007 32 1296-1299 Study on chemical constituents in rhigome of Ervatamia hainanensis LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . alstoyunine A C20H24N2O3 ÏàËÆ¶È:55% Journal of Natural Products 2009 72 1836-1841 Monoterpenoid Indole Alkaloids from Alstonia yunnanensis Tao Feng, Yan Li,Xiang-Hai Cai, Xun Gong, Ya-Ping Liu, Rong-Ting Zhang, Xiang-Yun Zhang, Qin-Gang Tan, and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 16-decarbomethoxyvinervinine ÏàËÆ¶È:55% Journal of Natural Products 1996 59 890-893 Indole Alkaloids of Haplophyton crooksii Mohamad A. Mroue, K. L. Euler, M. A. Ghuman, 2 and Maktoob Alam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 5,6-Dehydrocoronaridine ÏàËÆ¶È:55% Phytochemistry 1994 37 1729-1735 Indole alkaloids and terpenoids fromTabernaemontana markgrafiana Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 11-Methoxy isoretuline C22H28N2O3 ÏàËÆ¶È:55% Phytochemistry 1984 23 2659-2663 Dehydroisostrychnobiline, matopensine and other alkaloids from Strychnos kasengaensis Philippe Thepenier, Marie-Jos¨¦ Jacquier, Georges Massiot, Louisette Le Men-Olivier, Cl¨¦ment Delaude Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . Gardnerine ÏàËÆ¶È:55% Tetrahedron Letters 2005 46 4219-4224 First regiospecific, enantiospecific total synthesis of gardnerine and gardnutine Hao Zhou, Dongmei Han, Xuebin Liao, James M. Cook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 19-epi-voacanganne ÏàËÆ¶È:54.5% Planta Medica 1987 53 57-59 Indole Alkaloids from Trachelospermum jasminoides Atta-ur-Rahman, Talat Fatima, Mehrun-Nisa, S. Ijaz, George Crank and Shaheen Wasti Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . N4-methyl angustilobine B ÏàËÆ¶È:52.6% Phytochemistry 2005 66 1158-1162 Indole alkaloids from the leaves of Philippine Alstonia scholaris Allan Patrick G. Macabeo, Karsten Krohn, Dietmar Gehle, Roger W. Read, Joseph J. Brophy, Geoffrey A. Cordell, Scott G. Franzblau, Alicia M. Aguinaldo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . 19,20-(E)-vallesamine ÏàËÆ¶È:52.6% Phytochemistry 2005 66 1158-1162 Indole alkaloids from the leaves of Philippine Alstonia scholaris Allan Patrick G. Macabeo, Karsten Krohn, Dietmar Gehle, Roger W. Read, Joseph J. Brophy, Geoffrey A. Cordell, Scott G. Franzblau, Alicia M. Aguinaldo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . cyclo-(D-Leu-LTrp) C17H22O2N3 ÏàËÆ¶È:52.6% Journal of Natural Products 2005 68 237-239 Brevicompanine C, Cyclo-(d-Ile-l-Trp), and Cyclo-(d-Leu-l-Trp),Plant Growth Regulators from Penicillium brevi-compactum Yasuo Kimura, Aya Sawada, Masato Kuramata, Miyako Kusano, Shozo Fujioka, Tsuyoshi Kawano, and Atsumi Shimada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 19(S),20(R)-dihydroperaksine-17-al C18H22N2O ÏàËÆ¶È:52.6% Journal of Natural Products 2002 65 1006-1010 New Alkaloids of the Sarpagine Group from Rauvolfia serpentina Hairy Root Culture Yuri Sheludko,Irina Gerasimenko, Heinz Kolshorn, and Joachim St?ckigt Structure 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï2 1 . thodojaponia-4''-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:76.9% Chinese Traditional and Herbal Drugs 1996 27 262-265 Studies on the Chemical Constituents of Przewalsk Rhododendron(Rhododendron przewalskii) Jia Zhongjian and Li Guoqiang (Nation Laboratory of Applied Chemistry; Lanzhou University; Lanzhou); Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (+)-pinoresinol-4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:76.9% Journal of China Pharmaceutical University 2010 41 333-336 Chemical constituents from n-butanol extract of the stems of Lonicera japonica MA Rong; YIN Zhi-qi*; ZHANG Cong; YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (-)-(7R,7'R,7''R,8S,8'S,8''S)-4',4''-Dihydroxy-3,3',3'',5-tetramethoxy-7,9':7',9-diepoxy-4,8''-oxy-8,8'-sesquineolignan-7'',9''-diol C31H36O11 ÏàËÆ¶È:76.6% Journal of Natural Products 2011 74 1188-1200 Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations Liang Xiong, Chenggeng Zhu, Yanru Li, Ye Tian, Sheng Lin, Shaopeng Yuan, Jinfeng Hu, Qi Hou, Naihong Chen, Yongchun Yang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (-)-(7R,7'R,7''S,8S,8'S,8''S)-4',4''-Dihydroxy-3,3',3'',5-tetramethoxy-7,9':7',9-diepoxy-4,8''-oxy-8,8'-sesquineolignan-7'',9''-diol C31H36O11 ÏàËÆ¶È:76.6% Journal of Natural Products 2011 74 1188-1200 Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations Liang Xiong, Chenggeng Zhu, Yanru Li, Ye Tian, Sheng Lin, Shaopeng Yuan, Jinfeng Hu, Qi Hou, Naihong Chen, Yongchun Yang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . hedyotisol A ÏàËÆ¶È:75% Journal of Natural Products 2007 70 521-525 Mixed Lignan-Neolignans from Tarenna attenuata Xian-Wen Yang,Pei-Ji Zhao,Yan-Lin Ma, Hai-Tao Xiao, Yi-Qing Zuo, Hong-Ping He, Ling Li, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 4, 4'-dimethoxy-3'-hydroxy-7, 9'¡Ã7', 9-diepoxylignan-3-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:73.0% Acta Botanica Yunnanica 2003 25(6) 711-715 A New Lignan Glycoside from Curculigo capitulata LI Ning,TAN Ning-Hua,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (+)-pinoresinol O-¦Â-D-glucopyranoside ÏàËÆ¶È:73.0% Phytochemistry 2009 70 1277-1285 Absolute configuration of (+)-pinoresinol 4-O-[6''-O-galloyl]-¦Â-D-glucopyranoside,macarangiosides E, and F isolated from the leaves of Macaranga tanarius Katsuyoshi Matsunami, Hideaki Otsuka, Kazunari Kondo, Takakazu Shinzato, Masatoshi Kawahata, Kentaro Yamaguchi, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (+)-pinoresinol-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:73.0% Chemical & Pharmaceutical Bulletin 1987 35 4155-4161 Comparative Studies on the Constituents of a Parasitic Plant and Its Host. III. On the Constituents of Boschniakia rossica FEDTSCH. et FLEROV. (2) TENJI KONISHI,YOKO NARUMI,KAZUAKI WATANABE,SHIU KIYOSAWA and JUNZO SHOJI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . pinoresinol monoglucoside ÏàËÆ¶È:73.0% Phytochemistry 1989 28 1737-1741 Lignan glycosides from Parsonsia laevigata Fumiko Abe,Tatsuo Yamauchi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (+)-pinoresinol-O-¦Â-D-glucopyranoside ÏàËÆ¶È:73.0% Chinese Traditional and Herbal Drugs 2008 39 343-346 ÏãÁÛëާÖÐÄ¾Ö¬ËØÀ࿹Ñõ»¯»îÐԳɷֵÄÑо¿ ÕÅÑåÁú;ÔøÎ°Ãñ;Íõ»ÛÈÙ;ÖìÀö;ÐìºéÁÁ;¿ïº£Ñ§ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (+)-pinoresinol-O-¦Â-D-glucopyranoside ÏàËÆ¶È:73.0% Chinese Journal of Natural Medicines 2010 8 429-432 Chemical Constituents from the Flower of Datura metel YANG Bing-You; XIA Yong-Gang; CHEN Dong; KUANG Hai-Xue Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Pinoresinol-4-O-glucoside ÏàËÆ¶È:73.0% Archives of Pharmacal Research 2005 28 39-43 Antitumor and antiinflammatory constituents from celtis sinensis Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (-)-(7R,7'R,7''R,8S,8'S,8''S)-4',4''-Dihydroxy-3,3',3'',5,5'-pentamethoxy-7,9':7',9-diepoxy-4,8''-oxy-8,8'-sesquineolignan-7'',9''-diol C32H38O12 ÏàËÆ¶È:70% Journal of Natural Products 2011 74 1188-1200 Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations Liang Xiong, Chenggeng Zhu, Yanru Li, Ye Tian, Sheng Lin, Shaopeng Yuan, Jinfeng Hu, Qi Hou, Naihong Chen, Yongchun Yang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (-)-(7R,7'R,7''S,8S,8'S,8''S)-4',4''-Dihydroxy-3,3',3'',5,5'-pentamethoxy-7,9':7',9-diepoxy-4,8''-oxy-8,8'-sesquineolignan-7'',9''-diol C32H38O12 ÏàËÆ¶È:70% Journal of Natural Products 2011 74 1188-1200 Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations Liang Xiong, Chenggeng Zhu, Yanru Li, Ye Tian, Sheng Lin, Shaopeng Yuan, Jinfeng Hu, Qi Hou, Naihong Chen, Yongchun Yang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (+)-Pinoresinol-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:69.2% Acta Botanica Yunnanica 2006 28(4) 429-432 Non2alkaloid Constituents of Buxus sinica (Buxaceae) LIN Yun-Liang, QIU Ming-Hua, LI Zhong-Rong,ZHOU Lin,LIU Jian-Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (-)-pinoresinol 4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:69.2% China Journal of Chinese Materia Medica 2006 31 133-135 Chemical constituents from root of Lasianthus acuminatissimus I LI Bin, ZHANG Dongming, LUO Yongming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . pinoresinol-4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:69.2% Chinese Traditional and Herbal Drugs 2008 39 654-656 Chemical constituents of Selaginella sinensis FENG Wei-sheng; CHEN Hui; ZHENG Xiao-ke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 4,4'-dimethoxy-3'-hydroxy-7,9',7',9-diepoxyligan-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:69.2% Natural Product Research and Development 2010 22 731-735 Studies on the Chemical Constituents of Euphorbia helioscopia HE Jiang-bo;LIU Guang-ming; CHENG Yong-xian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (-)-(7R,7'R,7''R,8S,8'S,8''S)-4',4''-Dihydroxy-3,3',3'',5,5',5''-hexamethoxy-7,9':7',9-diepoxy-4,8''-oxy-8,8'-sesquineolignan-7'',9''-diol C33H40O13 ÏàËÆ¶È:66.6% Journal of Natural Products 2011 74 1188-1200 Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations Liang Xiong, Chenggeng Zhu, Yanru Li, Ye Tian, Sheng Lin, Shaopeng Yuan, Jinfeng Hu, Qi Hou, Naihong Chen, Yongchun Yang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (-)-(7R,7'R,7''S,8S,8'S,8''S)-4',4''-Dihydroxy-3,3',3'',5,5',5''-hexamethoxy-7,9':7',9-diepoxy-4,8''-oxy-8,8'-sesquineolignan-7'',9''-diol C33H40O13 ÏàËÆ¶È:66.6% Journal of Natural Products 2011 74 1188-1200 Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations Liang Xiong, Chenggeng Zhu, Yanru Li, Ye Tian, Sheng Lin, Shaopeng Yuan, Jinfeng Hu, Qi Hou, Naihong Chen, Yongchun Yang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . flacoside A C26H34O13 ÏàËÆ¶È:65.3% Planta Medica 2009 75 1246-1252 Investigation of Two Flacourtiaceae Plants: Bennettiodendron leprosipes and Flacourtia ramontchi Xing-Yun Chai, Hong-Yan Ren, Zheng-Ren Xu, Chang-Cai Bai, Fei-Ran Zhou, Si-Kai Ling, Xiao-Ping Pu, Fei-Fei Li,Peng-Fei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 2S,3R-2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-hydroxymethyl-7-methoxybenzofuran-5-(trans)-propen1-ol-3-O-¦Â-glucoside ÏàËÆ¶È:65.3% Natural Product Research and Development 2010 22 731-735 Studies on the Chemical Constituents of Euphorbia helioscopia HE Jiang-bo;LIU Guang-ming; CHENG Yong-xian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . antiarisin A C40H48O14 ÏàËÆ¶È:63.3% Planta Medica 2009 75 340-345 Phenylpropanoid and Lignan Derivatives from Antiaris toxicaria and their Effects on Proliferation and Differentiation of an Osteoblast-Like Cell Line Miao-Miao Jiang, Hao Gao, Yi Dai, Xue Zhang, Nai-LiWang, Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 5''-methoxyhedyotisol A C43H52O17 ÏàËÆ¶È:62.0% Journal of Natural Products 2007 70 521-525 Mixed Lignan-Neolignans from Tarenna attenuata Xian-Wen Yang,Pei-Ji Zhao,Yan-Lin Ma, Hai-Tao Xiao, Yi-Qing Zuo, Hong-Ping He, Ling Li, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . erythro¨Cguaiacylglycerol-¦Â-O-4'-(5')-methoxylariciresinol C31H38O11 ÏàËÆ¶È:62.0% Natural Product Research 2008 22 990-995 Sesquilignans and dilignans from Campylotropis hirtella (Franch.) Schindl. Hui-Ying Han; Hong-Wei Liu; Nai-Li Wang; Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . (7S, 8R) dehydrodiconiferyl alcohol 9'-¦Â-glucopyranoside ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 2001 49(8) 1036-1038 Studies on a Medicinal Parasitic Plant: Lignans from the Stems of Cynomorium songaricum Zhi-Hong JIANG,Takashi TANAKA, Masafumi SAKAMOTO,Tong JIANG,and Isao KOUNO Structure 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï3 1 . thero-2,3-bis-(4-hydroxy-3-methoxypheyl)-3-methoxy-propanol C18H22O6 ÏàËÆ¶È:94.4% Chinese Journal of Natural Medicines 2011 9 115-119 Chemical Constituents of Toona ciliata var. pubescens LIU Yu-Bo, CHENG Xiang-Rong, QIN Jiang-Jiang, YAN Shi-Kai, JIN Hui-Zi *, ZHANG Wei-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 1,2-bis(4-hydroxy-3-methoxyphenyl)-1,3-propanediol ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2010 35 2281-2284 Chemical constituents from rhizomes of Illicium henryi LIU Jifeng; ZHANG Xuemei; SHI Yao; JIANG Zhiyong; MA Yunbao; CHEN Jijun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 3 ÏàËÆ¶È:77.7% Journal of Natural Products 1998 61 1137-1139 Isolation and Absolute Structures of Enantiomeric 1, 2-Bis(4-hydroxy-3-methoxyphenyl)-1, 3-propanediol 1-O-Glucosides from the Bark of Hovenia trichocarpa Kazuko Yoshikawa, Noriko Mimura, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 1,2-Bis-(4-hydroxy-3-methoxyphenyl)-propane-1,3-diol C25H28O10 ÏàËÆ¶È:77.7% Phytochemistry 1980 19 449-453 Lignans of Larix leptolepis Keji Miki, Takashi Takehara, Takashi Sasaya, Akira Sakakibara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . erythro-2,3-Bis(4-hydroxy-3-methoxyphenyl)-3-ethoxypropan-1-ol C19H23O6 ÏàËÆ¶È:77.7% Archives of Pharmacal Research 2004 27 169-172 Phenolic compounds obtained from stems of couepia ulei with the potential to induce quinone reductase Dae Sik Jang, Eun Jung Park, Young-Hwa Kang, Jose Schunke Vigo and James G. Graham, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . carayensin-C C17H20O5 ÏàËÆ¶È:72.2% Bioorganic & Medicinal Chemistry Letters 2012 22 1895-1898 New antitumor compounds from Carya cathayensis Wei Wu, Xiu-Li Bi, Jia-Qing Cao, Kai-Qing Zhang, Yu-Qing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . lariciresinol 4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:70% Biochemical Systematics and Ecology 2004 32 1201-1204 Epoxylignans from the seeds of Centaurea cyanus (Asteraceae) Mohammad Shoeb, Marcel Jaspars, Stephen M. MacManus, Runner R. T. Majinda, Satyajit D. Sarker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (2R, 3S, 4S)-4-(4-hydroxy-3-methoxybenzyl)-2-(5-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-tetrahydrofuran-3-ol C20H24O7 ÏàËÆ¶È:70% Phytochemistry 2010 71 682-687 Chemical constituents from Saussurea cordifolia Xu-Wen Li, Zi-Tao Guo, Yun Zhao, Zheng Zhao, Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 8,8'-bis-(dirhydroconifery l)-diferuloylate C40H42O12 ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2010 41 867-870 ´óѪÌٵĻ¯Ñ§³É·ÖÑо¿(¢ò) ³ÂÖÇÏÉ;¸ßÎÄÔ¶;Áõá·ÁÕ;ÕÅÌú¾ü Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 1,2-diarylpropane-3-ol C17H20O5 ÏàËÆ¶È:66.6% Journal of Natural Products 2006 69 1218-1221 Secondary Metabolites from the Wood Bark of Durio zibethinus and Durio kutejensis Rudiyansyah, and Mary J. Garson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 3,4-dihydroxy-3',4'-dimethoxydeoxybenzoin C16H16O5 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2009 17 4360-4366 Potential antioxidants and tyrosinase inhibitors from synthetic polyphenolic deoxybenzoins Lean-Teik Ng, Horng-Huey Ko, Tzy-Ming Lu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 8R,8'R,9S-4,4',9-trihydroxy-3,3',-dimethoxy-9,9'-epoxylignan C20H24O6 ÏàËÆ¶È:65% Natural Product Research 2006 20 443-453 Lignans from Arnica species Thomas J. Schmidt; Sabine Stausberg; Jeanette Von Raison; Matthias Berner; G¨¹nter Willuhn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 8R,8'R,9R-4,4',9-trihydroxy-3,3',-dimethoxy-9,9'-epoxylignan C20H24O6 ÏàËÆ¶È:65% Natural Product Research 2006 20 443-453 Lignans from Arnica species Thomas J. Schmidt; Sabine Stausberg; Jeanette Von Raison; Matthias Berner; G¨¹nter Willuhn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . haplomarin ÏàËÆ¶È:65% Natural Product Research 2006 20 443-453 Lignans from Arnica species Thomas J. Schmidt; Sabine Stausberg; Jeanette Von Raison; Matthias Berner; G¨¹nter Willuhn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 1-(4-hydroxy-3-methoxy)-phenyl-2-[4-(2,3-dihydroxypropyl)-2-methoxy]-phenoxy-1,3-propandiol C20H26O9 ÏàËÆ¶È:65% Phytochemistry 1998 49 1299-1304 Antialgal compounds from zantedeschia aethiopica Marina Della Grec¦Á, Maria Ferrar¦Á, Antonio Fiorentino, Pietro Monaco, Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ |

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