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1 .     arctignan E
    ÏàËÆ¶È:65.8%
Chinese Journal of Natural Medicines          2006          4          444-447
Chemical Constituents of Antihyperglycemic Active Fraction from Arctium lappa
XU Zhao-Hui; ZHAO Ai-Hua; GAO Xian-Fu; JIA Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     ¡÷8',3,3',4-trymethoxy neolignan
    ÏàËÆ¶È:58.5%
Phytochemistry          1984          23          2025-2028
13C NMR spectral and conformational analysis of 8-O-4¡ä neolignans
Antonio C. Herrera Braga, Susana Zacchino, H¨¦ctor Badano, Manuel Gonz¨¢lez Sierra, Edmundo A. R¨²veda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Ramonanin A
C40H40O10     ÏàËÆ¶È:58.5%
Journal of Natural Products          2011          74          1293-1297
Spirocyclic Lignans from Guaiacum (Zygophyllaceae) Induce Apoptosis in Human Breast Cancer Cell Lines
Kathryn J. Chavez, Xiaohong Feng, James A. Flanders, Eloy Rodriguez, and Frank C. Schroeder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     rhyncoside E
C52H62O20     ÏàËÆ¶È:56.0%
Chemical & Pharmaceutical Bulletin          2007          55(8)          1175-1180
Rhyncosides A¡ªF, Phenolic Constituents from the Chinese Mangrove Plant Bruguiera sexangula var. rhynchopetala
Shuyun BAO,Yi DING,Zhiwei DENG,Peter PROKSCH,d an Wenhan LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     rhyncoside F
C52H62O20     ÏàËÆ¶È:56.0%
Chemical & Pharmaceutical Bulletin          2007          55(8)          1175-1180
Rhyncosides A¡ªF, Phenolic Constituents from the Chinese Mangrove Plant Bruguiera sexangula var. rhynchopetala
Shuyun BAO,Yi DING,Zhiwei DENG,Peter PROKSCH,d an Wenhan LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     arctignan G
C40H44O13     ÏàËÆ¶È:56.0%
Chemical & Pharmaceutical Bulletin          1996          44          2300-2304
Studies on Differentiation Inducers. VI.Lignan Derivatives from Arctium Fructus. (2)
Kaoru UMEHARA,Mitsuhiro NAKAMURA,Toshio MIYAKE,Masanori KUROYANAGI and Akira UENO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     arctignan H
C40H42O13     ÏàËÆ¶È:56.0%
Chemical & Pharmaceutical Bulletin          1996          44          2300-2304
Studies on Differentiation Inducers. VI.Lignan Derivatives from Arctium Fructus. (2)
Kaoru UMEHARA,Mitsuhiro NAKAMURA,Toshio MIYAKE,Masanori KUROYANAGI and Akira UENO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     arctignan D
C40H44O13     ÏàËÆ¶È:56.0%
Chemical & Pharmaceutical Bulletin          1993          41          1774-1779
Studies on Differentiation-Inducers from Arctium Fructus
Kaoru UMEHARA,Ariko SUGAWA,Masanori KUROYANAGI,Akira UENO and Takao TAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     lappaol F
    ÏàËÆ¶È:56.0%
Acta Pharmaceutica Sinica          1993          28          911-917
STUDIES ON THE CHEMICAL CONSTITUENTS OF ARCTIUM LAPPA L.
HY Wang and JS Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     1-(4-hydroxy-3-methoxyphenyl)-1,2,3-tris(4-allyl-2-methoxyphenoxy)propane
C30H32O6     ÏàËÆ¶È:56.0%
Chemical & Pharmaceutical Bulletin          2009          57          245-251
Leishmanicidal Active Constituents from Nepalese Medicinal Plant Tulsi (Ocimum sanctum L.)
Akiko Suzuki, Osamu Shirota, Kanami Mori, Setsuko Sekita, Hiroyuki Fuchino, Akihito Takano and Masanori Kuroyanagi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     lappaol H
    ÏàËÆ¶È:56.0%
Chinese Journal of Natural Medicines          2006          4          444-447
Chemical Constituents of Antihyperglycemic Active Fraction from Arctium lappa
XU Zhao-Hui; ZHAO Ai-Hua; GAO Xian-Fu; JIA Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     Lappaol F
    ÏàËÆ¶È:56.0%
Journal of China Pharmaceutical University          2003          34          116-118
Lignans from the Roots of Stellera chamaejasme
LIU Xin; YE Wen Cai; CHE Chun Tao; ZHAO Shou Xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




13 .     compound 2
C46H48O17     ÏàËÆ¶È:54.3%
Journal of Agricultural and Food Chemistry          2007          55          6460-6465
Inhibitory Activity against Tobacco Mosaic Virus (TMV) Replication of Pinoresinol and Syringaresinol Lignans and Their Glycosides from the Root of Rhus javanica var. roxburghiana
Ming-An Ouyang, Yung-Shung Wein, Zhen-Kun Zhang, and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     arctignan F
C40H42O3     ÏàËÆ¶È:53.6%
Chemical & Pharmaceutical Bulletin          1996          44          2300-2304
Studies on Differentiation Inducers. VI.Lignan Derivatives from Arctium Fructus. (2)
Kaoru UMEHARA,Mitsuhiro NAKAMURA,Toshio MIYAKE,Masanori KUROYANAGI and Akira UENO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     arctignan E
C40H44O13     ÏàËÆ¶È:53.6%
Chemical & Pharmaceutical Bulletin          1993          41          1774-1779
Studies on Differentiation-Inducers from Arctium Fructus
Kaoru UMEHARA,Ariko SUGAWA,Masanori KUROYANAGI,Akira UENO and Takao TAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




16 .     dimethylsecan- tioquine
    ÏàËÆ¶È:53.6%
Journal of Natural Products          1985          Vol 48          76-85
Alcaloëdes des Annonac¨¦es, LIII. Alcaloëdes du Pseudoxandra Aff. Lucida Etude de l'Antioquine et de Ses D¨¦riv¨¦s
Diego Cortes, Jairo Saez, Reynald Hocquemiller, Andr¨¦ Cav¨¦, Adrien Cav¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     lappaol F
    ÏàËÆ¶È:53.6%
China Journal of Chinese Materia Medica          2010          35          2852-2861
Constituents of Gymnadenia conopsea
YUE Zhenggang; ZI Jiachen; ZHU Chenggen; LIN Sheng; YANG Yongchun; SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     Corydaturtschine B
C39H40 N2O7     ÏàËÆ¶È:53.6%
Planta Medica          2010          76          1732-1738
New Cytotoxic Tetrahydroprotoberberine-Aporphine Dimeric and Aporphine Alkaloids from Corydalis turtschaninovii
Kim, Ki Hyun; Piao, Cheng Jie; Choi, Sang Un; Son, Mi Won; Lee, Kang Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




19 .     (+)-(7R,7'R,7''R,7'''R,8S,8'S,8''S,8'''S)-4'',4'''-Dihydroxy-3,3',3'',3''',5,5'-hexamethoxy-7,9':7',9-diepoxy-4,8'':4',8'''-bisoxy-8,8'-dineolignan-7'',7''',9'',9'''-tetraol
C42H50O16     ÏàËÆ¶È:53.6%
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''R,7'''S,8S,8'S,8''S,8'''S)-4'',4'''-Dihydroxy-3,3',3'',3''',5,5'-hexamethoxy-7,9':7',9-diepoxy-4,8'':4',8'''-bisoxy-8,8'-dineolignan-7'',7''',9'',9'''-tetraol
C42H50O16     ÏàËÆ¶È:53.6%
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 .     Ramonanin D
C40H40O10     ÏàËÆ¶È:53.6%
Journal of Natural Products          2011          74          1293-1297
Spirocyclic Lignans from Guaiacum (Zygophyllaceae) Induce Apoptosis in Human Breast Cancer Cell Lines
Kathryn J. Chavez, Xiaohong Feng, James A. Flanders, Eloy Rodriguez, and Frank C. Schroeder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




22 .     compound 4
C42H38O22     ÏàËÆ¶È:52.3%
Journal of Agricultural and Food Chemistry          2002          50          2524-2530
Structural Identification of New Curcumin Dimers and Their Contribution to the Antioxidant Mechanism of Curcumin
Toshiya Masuda, Yukiko Toi, Hiromi Bando, Tomomi Maekawa, Yoshio Takeda, and Hidemasa Yamaguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




23 .     compound 3
C46H48O17     ÏàËÆ¶È:52.1%
Journal of Agricultural and Food Chemistry          2007          55          6460-6465
Inhibitory Activity against Tobacco Mosaic Virus (TMV) Replication of Pinoresinol and Syringaresinol Lignans and Their Glycosides from the Root of Rhus javanica var. roxburghiana
Ming-An Ouyang, Yung-Shung Wein, Zhen-Kun Zhang, and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




24 .     berpodine
C40H38N2O13     ÏàËÆ¶È:51.2%
Chemistry of Natural Compounds          1996          32          216-334
ALKALOIDS. PLANTS, STRUCTURE, PROPERTIES
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




25 .     (-)-(7'S,8'S)-threo-carolignan X
C39H40O12     ÏàËÆ¶È:51.2%
Journal of Natural Products          2010          73          1649-1654
Lignans and Triterpenes from the Bark of Durio carinatus and Durio oxleyanus
Rudiyansyah, Lynette K. Lambert, and Mary J. Garson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




26 .     O-methylthalicberine
    ÏàËÆ¶È:51.2%
Chinese Journal of Natural Medicines          2009          7          293-296
Chemical Constituents from Thalictrum fortunei
ZHANG Xian-Tao; ZHANG Lei-Hong; WANG Ying; LI Yan; WANG Yu-Sheng; YE Wen-Cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




27 .     3-benzyloxy-8,9-dihydro-2,11,12-trimethoxy-14-[4-methoxy-3-(methoxymethoxy)phenyl]-6H-[1]benzopyrano[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one
C38H35NO9     ÏàËÆ¶È:51.2%
Bioorganic & Medicinal Chemistry          2011          19          7541-7550
Synthesis, structure¨Cactivity relationships, and mechanism of action of anti-HIV-1 lamellarin ¦Á 20-sulfate analogues
Haruka Kamiyama, Yoshinao Kubo, Hironori Sato, Naoki Yamamoto, Tsutomu Fukuda, Fumito Ishibashi, Masatomo Iwao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




28 .     (+)-(7R,7'R,7''S,7'''S,8S,8'S,8''S,8'''S)-4'',4'''-Dihydroxy-3,3',3'',3''',5,5'-hexamethoxy-7,9':7',9-diepoxy-4,8'':4',8'''-bisoxy-8,8'-dineolignan-7'',7''',9'',9'''-tetraol
C42H50O16     ÏàËÆ¶È:51.2%
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

--------------------------------------------------------------------------------




29 .     compound 2
C42H38O12     ÏàËÆ¶È:51.2%
Journal of Agricultural and Food Chemistry          1999          47          71-75
Chemical Studies on Antioxidant Mechanism of Curcuminoid:  Analysis of Radical Reaction Products from Curcumin
Toshiya Masuda, Kayo Hidaka, Ayumi Shinohara, Tomomi Maekawa, Yoshio Takeda, and Hidemasa Yamaguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




30 .     compound 5
C42H38O22     ÏàËÆ¶È:50%
Journal of Agricultural and Food Chemistry          2002          50          2524-2530
Structural Identification of New Curcumin Dimers and Their Contribution to the Antioxidant Mechanism of Curcumin
Toshiya Masuda, Yukiko Toi, Hiromi Bando, Tomomi Maekawa, Yoshio Takeda, and Hidemasa Yamaguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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