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²éѯ½á¹û£º¹²²éµ½104¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (7R,8S)-7-(4-hydroxy-3-methoxyphenyl)-8-(4-(3-(hydroxymethyl)-5-(3-(E)-hydroxyprop-1-enyl)-7-methoxybenzofuran-2-yl)-2-methoxyphenoxy)propane-7,9-diol C30H32O10 ÏàËÆ¶È:66.6% Fitoterapia 2009 80 320-326 Three lignans and one coumarinolignoid with quinone reductase activity from Eurycorymbus cavaleriei Zhongjun Ma, Xiaoyu Zhang, Lin Cheng, Peng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (7R, 8R)-7-(4-hydroxy-3-methoxyphenyl)-8-(4-(3-(hydroxymethyl)-5-(3-(E)-hydroxyprop-1-enyl)-7-methoxybenzofuran-2-yl)-2-methoxyphenoxy)propane-7,9-diol C30H32O10 ÏàËÆ¶È:63.3% Fitoterapia 2009 80 320-326 Three lignans and one coumarinolignoid with quinone reductase activity from Eurycorymbus cavaleriei Zhongjun Ma, Xiaoyu Zhang, Lin Cheng, Peng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (7R,8R,8'R)-4'-guaiacylglyceryl-Evofolin B C27H30O10 ÏàËÆ¶È:62.0% Fitoterapia 2014 94 29-35 New lignans from the bioactive fraction of Sambucus williamsii Hance and proliferation activities on osteoblastic-like UMR106 cells Hui-hui Xiao, Yi Dai, Man-sau Wong, Xin-sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . threo-5-[1-[4-[(1E)-2-(3,5-Dihydroxyphenyl)ethenyl]-3-methoxyphenoxy]-2-methoxy-2-(4-hydroxy-3-methoxyphenyl)ethyl]-1,3-benzenediol C31H30O9 ÏàËÆ¶È:62.0% Journal of Asian Natural Products Research 2014 16 511-521 Biomimetic synthesis of active isorhapontigenin dimers Xian-Fen Wang, Yuan Zhang, Ming-Bao Lin, Qi Hou, Chun-Suo Yao & Jian-Gong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . erythro-5-[1-[4-[(1E)-2-(3,5-Dihydroxyphenyl)ethenyl]-3-methoxyphenoxy]-2-methoxy-2-(4-hydroxy-3-methoxyphenyl)ethyl]-1,3-benzenediol C31H30O9 ÏàËÆ¶È:62.0% Journal of Asian Natural Products Research 2014 16 511-521 Biomimetic synthesis of active isorhapontigenin dimers Xian-Fen Wang, Yuan Zhang, Ming-Bao Lin, Qi Hou, Chun-Suo Yao & Jian-Gong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 7',8'-didehydroherpetotriol C30H30O9 ÏàËÆ¶È:60% Chinese Chemical Letters 2008 19 1215-1217 Two new lignans from Dipteronia dyeriana Rong Guo, Min Luo, Chun Lin Long, Ma Lin Li, Zhi Qin Ouyang, Yi Ping Zhou, Yue Hu Wang , Xing Yu Li , Ya Na Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (+)lariciresinol-9¡¯-ferulate C30H32O9 ÏàËÆ¶È:60% Chemistry & Biodiversity 2011 8 2299-2309 Phenolic Compounds of Abies nephrolepis and Their NO Production Inhibitory Activities (pages 2299¨C2309) Yong-Li Li, Liang Wu, Dan-Wei Ouyang, Ping Yu, Jia-Han Xia, Yue-Xing Pan, Xian-Wen Yang, Hua-Wu Zeng, Xiang-Rong Cheng, Hui-Zi Jin and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (E)-2,2',5'-Trihydroxystilbene C14H12O3 ÏàËÆ¶È:58.6% Bioorganic & Medicinal Chemistry 2011 19 5155-5166 Synthesis and antimicrobial activity of (E) stilbene derivatives Sabrina Albert, Ralf Horbach, Holger B. Deising, Bianka Siewert, Ren¨¦ Csuk Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Hibiscuwanin B C28H27NO7 ÏàËÆ¶È:58.6% Bioorganic & Medicinal Chemistry 2004 12 2193-2197 Cytotoxicity of phenylpropanoid esters from the stems of Hibiscus taiwanensis Pei-Lin Wu, Ta-Hsien Chuang, Cai-Xia He, Tian-Shung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2,7,2'-trihydroxy-4,4',7'-trimethoxy-1,1'-biphenanthrene C31H24O6 ÏàËÆ¶È:58.0% Journal of Natural Products 2006 69 907-913 Mono-, Bi-, and Triphenanthrenes from the Tubers of Cremastra appendiculata Zhen Xue, Shuai Li, Sujuan Wang, Yinhong Wang, Yongchun Yang, Jiangong Shi, and Lan He Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . cirrhopetalanthrin ÏàËÆ¶È:56.6% Journal of Natural Products 2006 69 907-913 Mono-, Bi-, and Triphenanthrenes from the Tubers of Cremastra appendiculata Zhen Xue, Shuai Li, Sujuan Wang, Yinhong Wang, Yongchun Yang, Jiangong Shi, and Lan He Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (+)-isolariciresinol-9¡¯-ferulate C30H32O9 ÏàËÆ¶È:56.6% Chemistry & Biodiversity 2011 8 2299-2309 Phenolic Compounds of Abies nephrolepis and Their NO Production Inhibitory Activities (pages 2299¨C2309) Yong-Li Li, Liang Wu, Dan-Wei Ouyang, Ping Yu, Jia-Han Xia, Yue-Xing Pan, Xian-Wen Yang, Hua-Wu Zeng, Xiang-Rong Cheng, Hui-Zi Jin and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . chrysophaentin A C32H24Cl4O8 ÏàËÆ¶È:56.6% Journal of the American Chemical Society 2010 132 9069-9077 Chrysophaentins A−H, Antibacterial Bisdiarylbutene Macrocycles That Inhibit the Bacterial Cell Division Protein FtsZ Alberto Plaza, Jessica L. Keffer, Giuseppe Bifulco, John R. Lloyd and Carole A. Bewley Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . [3,4,5,6-(13)C4] 1-(2-carboxy-4-hydroxyphenyl)-E-4-(4-hydroxy-3-methoxybenzylidene)-2-(4-hydroxy-3-methoxyphenyl)-5-oxopyrrolidine-3-carbamoyl-5-hydroxyanthranilate ÏàËÆ¶È:56.2% Tetrahedron 2004 60 4765-4771 Identification of a dehydrodimer of avenanthramide phytoalexin in oats Yozo Okazaki, Atsushi Ishihara, Takaaki Nishioka, Hajime Iwamura Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 16 C32H31NO10 ÏàËÆ¶È:56.2% European Journal of Organic Chemistry 2011 100-109 Tandem Ugi MCR/Mitsunobu Cyclization as a Short, Protecting-Group-Free Route to Benzoxazinones with Four Diversity Points Luca Banfi, Andrea Basso, Lorenzo Giardini, Renata Riva, Valeria Rocca and Giuseppe Guanti Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . cannabisin D C36H34N2O8 ÏàËÆ¶È:56.2% Chinese Traditional and Herbal Drugs 2013 44 1877-1880 Chemical constituents from seeds of Datura metel (I) YANG Bing-you, LIU Yan, WANG Xin, XIA Yong-gang, WANG Qiu-hong, KUANG Hai-xue Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . pangkorimine C34H32N2O6 ÏàËÆ¶È:55.8% The Chinese Pharmaceutical Journal 2003 55 35-47 Chemical Constituents from Dehaasia triandra. III. Bisbenzylisoquinoline Alkaloids from the Leaves and Their Conformational Analysis Chien-Kuang Chen, Shoei-Sheng Lee and Chung-Hsiung Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (+)-lariciresinol 9'-p-coumarate C29H30O8 ÏàËÆ¶È:55.1% Journal of Natural Products 2005 68 1175-1179 Lignans from Bark of Larix olgensis var. koreana Bao-Hua Yang, Wei-Dong Zhang, Run-Hui Liu, Ting-Zhao Li, Chuan Zhang, Yun Zhou, and Juan Su Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (-)-7-hydroxylariciresinol 9'-p-coumarate C29H30O9 ÏàËÆ¶È:55.1% Journal of Natural Products 2005 68 1175-1179 Lignans from Bark of Larix olgensis var. koreana Bao-Hua Yang, Wei-Dong Zhang, Run-Hui Liu, Ting-Zhao Li, Chuan Zhang, Yun Zhou, and Juan Su Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . agastenol C27H26O8 ÏàËÆ¶È:55.1% Journal of Natural Products 2002 65 414-416 Agastinol and Agastenol, Novel Lignans from Agastache rugosa and Their Evaluation in an Apoptosis Inhibition Assay Choonghwan Lee, Hyuna Kim, and Yunghee Kho Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Glehnilate C24H22O7 ÏàËÆ¶È:55.1% Chinese Chemical Letters 2002 13 147-150 Biphenyl Ferulate from Glehnia littoralis Zhong YUAN, Shigetoshi KADOTA, Xian LI Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . sambucunol A C29H32O10 ÏàËÆ¶È:55.1% Journal of Asian Natural Products Research 2007 9 463-471 Lignans from the stems of Sambucus williamsii and their effects on osteoblastic UMR106 cells XU-JUAN YANG, MAN-SAU WONG, NAI-LI WANG, SUN-CHI CHAN and XIN-SHENG YAO Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . sambucunol B C29H32O10 ÏàËÆ¶È:55.1% Journal of Asian Natural Products Research 2007 9 463-471 Lignans from the stems of Sambucus williamsii and their effects on osteoblastic UMR106 cells XU-JUAN YANG, MAN-SAU WONG, NAI-LI WANG, SUN-CHI CHAN and XIN-SHENG YAO Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . sambucunol A C29H32O10 ÏàËÆ¶È:55.1% Journal of Asian Natural Products Research 2007 9 583-591 Lignans from the stems of Sambucus williamsii and their effects on osteoblastic UMR106 cell XU-JUAN YANG, MAN-SAU WONG, NAI-LI WANG, SUN-CHI CHAN and XIN-SHENG YAO Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . sambucunol B C29H32O10 ÏàËÆ¶È:55.1% Journal of Asian Natural Products Research 2007 9 583-591 Lignans from the stems of Sambucus williamsii and their effects on osteoblastic UMR106 cell XU-JUAN YANG, MAN-SAU WONG, NAI-LI WANG, SUN-CHI CHAN and XIN-SHENG YAO Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . kumujansine C28H25N4O2Cl ÏàËÆ¶È:55.1% Acta Pharmaceutica Sinica 1988 Vol 23 267-272 KUMUJANSINE AND KUMUJANTINE, TWO NEW DIMERIC ¦Â-CARBOLINE ALKALOIDS FROM PICRASMA QUASSIOIDES (D.DON.) BENN. JS Yang; DQ Yu and XT Liang Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 4-O-8'/4'-O-8''-Didehydrotriferulic acid (Triferulic acid) C30H24O12 ÏàËÆ¶È:55.1% Fitoterapia 2011 82 950-954 Irbic acid, a dicaffeoylquinic acid derivative from Centella asiatica cell cultures Fabiana Antognoni, Nicoletta Crespi Perellino, Sergio Crippa, Roberto Dal Toso, Bruno Danieli, Anacleto Minghetti, Ferruccio Poli, Giovanna Pressi Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (E)-2',3,4,5'-Tetrahydroxystilbene C14H12O4 ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2011 19 5155-5166 Synthesis and antimicrobial activity of (E) stilbene derivatives Sabrina Albert, Ralf Horbach, Holger B. Deising, Bianka Siewert, Ren¨¦ Csuk Structure 13C NMR ̼Æ×Ä£Äâͼ |

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