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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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×ÏËÕÒ»ÓÄÏã: ½ð±Ò+30, ¡ï¡ï¡ïºÜÓаïÖú 2012-06-17 22:18:53
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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