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²éѯ½á¹û£º¹²²éµ½261¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Spathulatol ÏàËÆ¶È:76.6% Acta Botanica Yunnanica 2010 32 281-284 One New Sesqui-lignan from Illicium spathulatum (Ill iciaceae) LAI Guo-Fang, DONG Xu-Jun, YANG Jian-Kun , LUO Huai-Rong, WANG Yi-Fen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . lappaol A ÏàËÆ¶È:76.6% Chinese Pharmaceutical Journal 2009 44 1287-1290 Studies on Chemical Constituents from Rhaponticum carthamoides (Willd.) Iljin HUANG Min-fang, LI Ning, NI Hui, JIA Xiao-guang*, LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3-hydroxymethyl-5-(3-hydroxypropyl)-7-methoxy-2-{3-methoxy-4-[1-(3,4-dimethoxybenzyl)-2-hydroxyethyl]phenyl}-2,3-dihydrobenzofuran C31H38O8 ÏàËÆ¶È:74.1% Journal of Natural Products 1999 62 1371-1375 New Metabolites from Onopordum illyricum Alessandra Braca, Nunziatina De Tommasi, Ivano Morelli, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . sesquipinsapol B ÏàËÆ¶È:72.4% Chinese Traditional and Herbal Drugs 2010 41 533-536 Â黯¸ùµÄ»¯Ñ§³É·ÖÑо¿ ÌÕ»ªÃ÷;ÍõÁ¥Êé;´ÞÕ¼³¼;ÕÔ´óÇì;ÁõÓÀºê Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Seslignanoccidentaliol A C31H38O11 ÏàËÆ¶È:70% Helvetica Chimica Acta 2010 93 1795-1802 Anthraquinones and Lignans from Cassia occidentalis Shi-Fei Li, Ying-Tong Di, Yue-Hu Wang, Cheng-Jian Tan, Xin Fang, Yu Zhang, Yong-Tang Zheng, Ling Li, Hong-Ping He, Shun-Lin Li and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 5 ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 7 . compound 6 ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 8 . (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: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 -------------------------------------------------------------------------------- 9 . lappaol A ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 10 . 7'-Hydroxyisolappaol A ÏàËÆ¶È:66.6% Pharmazie 2004 59 972-976 Sesquiterpenes, lignans and other constituents from Saussurea macrota Min Yang, Chun-Ming Wang, Qi Zhang, Yi-Feng Han, and Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . trans-5-(3-hydroxypropyl)-7-methoxy-2-[2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(3-methoxy-4-hydroxyphenyl)-benzofuran-5-yl]benzofuran C29H30O8 ÏàËÆ¶È:65.5% Planta Medica 2005 71 847-851 Four New Benzofurans from Seeds of Styrax perkinsiae Qi-Lin Li,Bo-Gang Li,Hua-Yi Qi,Xiao-Ping Gao,Guo-Lin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . erythro¨Cguaiacylglycerol-¦Â-O-4'-(5')-methoxylariciresinol C31H38O11 ÏàËÆ¶È:65.5% 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 -------------------------------------------------------------------------------- 13 . acernikol ÏàËÆ¶È:65.5% Chinese Traditional and Herbal Drugs 2010 41 863-866 Chemical constituents in stems of Schima superba XU Wen; ZHOU Guang-xiong; DAI Yi; YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (7R,8S)-dihydrodehydrodiconiferyl alcohol 9'-O-¦Â-D-glucopyranoside ÏàËÆ¶È:65.5% Chinese Traditional and Herbal Drugs 2009 40 1039-1042 ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿ »ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 2,3-dihydro-2-(4'-O-¦Â-D-glucopyranosyl-3'-methoxy-phenyl)-3-hydroxymethyl-5-(3-hydroxypropyl)-7-methoxybenzofuran ÏàËÆ¶È:65.5% Chinese Traditional and Herbal Drugs 2003 34 496-498 Studies on water-soluble constituents in rhizome of Polygonum cuspidatum XIAO Kai; XUAN Li-jiang; XU Ya-ming; BAI Dong-lu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . deltoignan B C29H30O9 ÏàËÆ¶È:65.5% Fitoterapia 2012 83 1125-1130 Cytotoxic sesquiterpenes and lignans from Saussurea deltoidea Jun-Ju Xu, Huo-Qiang Huang, Guang-Zhi Zeng, Ning-Hua Tan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (7'R,8'S)-dihydrodehydrodiconiferyl alcohol 4'-O-¦Â-Dglucopyranoside ÏàËÆ¶È:65.5% Chinese Traditional and Herbal Drugs 2011 42 25-30 Lignans and flavonoids from rhizome of Drynaria fortunei LIANG Yong-hong, YE Min, HAN Jian, WANG Bao-rong, GUO De-an Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . berbikonol C32H40O11 ÏàËÆ¶È:64.5% Bioorganic & Medicinal Chemistry Letters 2011 21 2270-2273 Biological evaluation of phenolic constituents from the trunk of Berberis koreana Ki Hyun Kim,Eunjung Moon,Sang Un Choi , Sun Yeou Kim , Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 4 ÏàËÆ¶È:63.3% 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 -------------------------------------------------------------------------------- 20 . compound 3a ÏàËÆ¶È:63.3% Acta Botanica Sinica 1998 40 466-469 Studies on the Lignans of Polygonum Orientale ZHENG Shang-Zhen, WANG Ding-Yong, MENG Jun-Cai, SHEN Xu-Wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . vitrifol A C30H34O9 ÏàËÆ¶È:63.3% Journal of Asian Natural Products Research 2008 10 499-502 One new dihydrobenzofuran lignan from Vitex trifolia Qiong Gu, Xue-Mei Zhang, Jun Zhou, Sheng-Xiang Qiu and Ji-Jun Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (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: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 -------------------------------------------------------------------------------- 23 . picrasmalignan A C30H30O9 ÏàËÆ¶È:63.3% Chemistry & Biodiversity 2011 Vol.8 1163-1169 A New Neolignan and a New Sesterterpenoid from the Stems of Picrasma quassioides Bennet Wei-Hua Jiao, Hao Gao, Feng Zhao, Fei He, Guang-Xiong Zhou, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . clinopodic acid H C29H26O12 ÏàËÆ¶È:62.0% Journal of Natural Products 2009 72 1379-1384 Matrix Metalloproteinase-2 Inhibitors from Clinopodium chinense var. parWiflorum Toshihiro Murata,Kenroh Sasaki,Kumiko Sato, Fumihiko Yoshizaki, Haruna Yamada, Hiromichi Mutoh, Kaoru Umehara,Toshio Miyase,Tsutomu Warashina,Hiroaki Aoshima, Homare Tabata, and Kouichi Matsubara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . dihydrodehydrodiconiferyl alcohol 4'-O-¦Â-D-glucoside C20H24O6 ÏàËÆ¶È:62.0% Chemical & Pharmaceutical Bulletin 1986 34 4340-4345 Lignans from Trachelospermum asiaticum (Tracheolospermum. II) FUMIKO ABE and TATSUO YAMAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . dihydrodehydrodiconiferyl alcohol 9'-O-glucoside C26H34O11 ÏàËÆ¶È:62.0% Chemical & Pharmaceutical Bulletin 1986 34 4340-4345 Lignans from Trachelospermum asiaticum (Tracheolospermum. II) FUMIKO ABE and TATSUO YAMAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . hanultarin C30H34O9 ÏàËÆ¶È:62.0% Natural Product Sciences 2009 15 17-21 Lignans from the Roots of Berberis amurensis Park, Hyun-Bong; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Il-Kyun; Noh, Hyung-Jun; Choi, Sang-Un; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . (7S,8R)-dihydrodehydrodiconiferyl alcohol 4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:62.0% Chinese Traditional and Herbal Drugs 2009 40 1039-1042 ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿ »ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . 2,3-¶þÇâ-2-(4-O-¦Â-D ßÁà«ÆÏÌÑÌÇ»ù-3'-¼×Ñõ»ù-±½»ù)-3-ôǼ׻ù-5-(3'-ôÇ»ù±û»ù)-7-¼×Ñõ»ù±½ßò߻ૠÏàËÆ¶È:62.0% Journal of Shenyang Pharmaceutical University 2009 26 279-281 Chemical constituents of the leaves of Crataegus pinnatifida Bge. HAO Dong-fang, YANG Rui-ping, ZHOU Yu-zhi, CHEN Huan, LI Zhi-feng, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . compound 13 ÏàËÆ¶È:62.0% Journal of Agricultural and Food Chemistry 2003 51 6165-6172 Lignans and Neolignans from Brassica fruticulosa: Effects on Seed Germination and Plant Growth Francesca Cutillo, Brigida D'Abrosca, Marina DellaGreca, Antonio Fiorentino, and Armando Zarrelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . dihydrodehydrodiconiferylalcohol-¦Â-D-(2'-O-p-hydroxybenzoyl)glucoside C33H38O13 ÏàËÆ¶È:60.6% Chemical & Pharmaceutical Bulletin 1998 46 655-662 Pharmacologically Active Components of Viticis Fructus (Vitex rotundifolia). II. The Component Having Analgesic Effects Emi OKUYAMA,Shigeru FUJIMORI,Mikio YAMAZAKI and Takeshi DEYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . dumosaol C30H32O10 ÏàËÆ¶È:60% Acta Botanica Yunnanica 2005 27(2) 217-222 A New Sesquilignan from Tsuga dumosa ZHAO You-Xing, LI Cheng-Sen, LUO Xiao-Dong,LIU Yu-Qing,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . 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 -------------------------------------------------------------------------------- 34 . L'herpetotriol C27H19O2(OCH3)3(OH)4 ÏàËÆ¶È:60% Tetrahedron letters 1978 19 4111-4112 Structure de l'herpetotriol, sesquilignane trimere de l'alcool coniferylique, isole d'herpetospermum caudigerum wall. Jean Favre-Bonvin, Mourad Kaouadji, Anne-Marie Mariotte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . (+)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 -------------------------------------------------------------------------------- 36 . saccharumoside A C34H40O14 ÏàËÆ¶È:58.8% Journal of Natural Products 2011 74 2472-2476 Phenolic Glycosides from Sugar Maple (Acer saccharum) Bark Tao Yuan, Chunpeng Wan, Antonio Gonz¨¢lez-Sarr¨ªas, Vamsikrishna Kandhi, Nadja B. Cech, and Navindra P. Seeram Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . 3-benzofuranmethanol-2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-4-methoxy-6-[tetrahydro-2-(3-hydroxy-4-methoxyphenyl)-3-methanol]-2-furanmethyl C30H35O9 ÏàËÆ¶È:58.6% Chemical & Pharmaceutical Bulletin 2006 54(11) 1592-1594 Hepatitis B Virus Inhibiting Constituents from Herpetospermum caudigerum Hai-Long YUAN,Ming YANG,Xian-Yi LI,Rong-Hui YOU,Yi LIU,Jun ZHU,Huan XIE,and Xiao-He XIAO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . grossamide K C28H29NO7 ÏàËÆ¶È:58.6% Phytochemistry 2001 58 1219-1223 Lignanamides and other phenolic constituents from the bark of kenaf (Hibiscus cannabinus) Ana M. L. Seca, Artur M. S. Silva, Armando J. D. Silvestre, Jos¨¦. A. S. Cavaleiro,Fernando M. J. Domingues, Carlos Pascoal-Neto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . agastinol C27H28O8 ÏàËÆ¶È:58.6% 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 -------------------------------------------------------------------------------- 40 . compound 4 ÏàËÆ¶È:58.6% Chemical & Pharmaceutical Bulletin 1984 32 4653-4657 Effects of O-Methylation and O-Glucosylation on Carbon-13 Nuclear Magnetic Resonance Chemical Shifts of Matairesinol, (+)-Pinoresinol and (+)-Epipinoresinol SANSEI NISHIBE,HIROKI TSUKAMOTO and SUEO HISADA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . herpetin ÏàËÆ¶È:58.6% Journal of Chinese Pharmaceutical Sciences 2005 14 140-143 Herpetin, a New Bioactive Lignan Isolated from Herpetospermum caudigerum YUAN Hai-long; LIU Yi; ZHAO Yan-ling; and XIAO Xiao-he Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . isoriccardinquinone B C29H24O5 ÏàËÆ¶È:58.6% Natural Product Research 2002 16 167-171 Two New Cyclic Bis(Bibenzyl)s, Isoriccardinquinone A and B from the Liverwort Marchantia Paleacea May-Ling So; Wing-Hong Chan; Ping-Fang Xia; Yuxin Cui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . umbroside C25H32O11 ÏàËÆ¶È:58.6% Acta Pharmaceutica Sinica 1999 Vol 34 297-300 CHEMICAL CONSTITUENTS FROM THE RHIZOMES OF PHLOMIS UMBROSA TURCZ Fu Hongzheng (Fu HZ); Liu Shiwang (Liu SW) and Lin Wenhan (Lin WH) Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . cerberalignan E C30H34O10 ÏàËÆ¶È:58.6% Phytochemistry 1988 27 3627-3631 Sesqui-,sester-and trilignans from stems of Cerbera manghas and C. odollam Fumiko Abe,Tatsuo Yamauchi,Alfred S.C. Wan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . epipinoresinol 4'-O-glucoside ÏàËÆ¶È:58.6% Phytochemistry 1990 29 1971-1980 Lignans of Forsythia intermedia Maiada M.A. Rahman,Paul M. Dewick,David E. Jackson,John A. Lucas Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . quinquenin L1 ÏàËÆ¶È:58.6% Chinese Traditional and Herbal Drugs 2001 32 15-17 Î÷Ñó²Î¾¥Ò¶ÖеÄÒ»ÖÖÄ¾Ö¬ËØ Íõ½ð»Ô,ºî°ØÁá,Àîϳ,ɳÒÊ!±¾Ð£·ÖÎö²âÊÔÖÐÐÄ,ÀîÎÄ!±¾Ð£·ÖÎö²âÊÔÖÐÐÄ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . (+)lariciresinol 4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:58.6% Chinese Journal of Natural Medicines 2003 1 199-203 Studies on Lignan Constituents of Clematis armandii Franch HUANG Wen-Wu; KONG De-Yun; YANG Pei-Ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . woonenoside XI ÏàËÆ¶È:58.6% Chinese Journal of Medicinal Chemistry 2010 20 304-309 The lignans from Daphne giraldii Nitsche LIU Wen-juan, WANG Li-bo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . N-(2,5-dimethoxyphenyl)methyl-N-methyl-trans-3-phenylsulfanylacrylamide C19H21NO3S ÏàËÆ¶È:58.6% Heterocycles 2002 57 1063-1077 Synthesis of 1,2-Dihydrobenz[c]azepin-3-one via Acid-catalyzed Cyclization of N-Arylmethyl-N-methyl-3-phenylsulfanylacrylamide Yoshie Horiguchi,* Toshiaki Saitoh, Tomoko Kashiwagi, Lisa Katura, Mayumi Itagaki, Jun oda, and Takehiro Sano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . compound 7 C33H34O6Br2 ÏàËÆ¶È:58.6% Heterocycles 2001 54 259-274 Total Syntheses of Plagiochins A and D, Macrocyclic Bis(bibenzyls), by Pd(0) Catalyzed Intramolecular Stille-Kelly Reaction1 Yoshiyasu Fukuyama,* Hideyuki Yaso, Takashi Mori, Hironobu Takahashi, Hiroyuki Minami, and Mitsuaki Kodama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 51 . acernikol C31H38O11 ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 2003 51(1) 62-67 Medicinal Foodstuffs. XXXI. Structures of New Aromatic Constituents and Inhibitors of Degranulation in RBL-2H3 Cells from a Japanese Folk Medicine, the Stem Bark of Acer nikoense Toshio MORIKAWA, Jing TAO, Kazuho UEDA, Hisashi MATSUDA, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 52 . 3-[2-(3,4-dimethoxyphenyl)ethyl]-3,4-dihydro-1-(3-hydroxy-4-methoxyphenyl)-8-methoxy-4-oxo-[1]benzopyrano[3,4-b]pyrrol-7-yl 2,2,2-trichloroethyl sulfate C31H28Cl3NO11S ÏàËÆ¶È:58.0% 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 |

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