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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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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