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²éѯ½á¹û£º¹²²éµ½7861¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 3a ÏàËÆ¶È:100% Phytochemistry 2008 69 788-795 Neolignan glycosides from Symplocos caudata Changhong Huo, Hong Liang, Yuying Zhao, Bin Wang, Qingying Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 4a ÏàËÆ¶È:100% Phytochemistry 2008 69 788-795 Neolignan glycosides from Symplocos caudata Changhong Huo, Hong Liang, Yuying Zhao, Bin Wang, Qingying Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]-propane-1,3-diol C20H26O7 ÏàËÆ¶È:100% Molecules 2008 13 1219-1229 Identification of Minor Secondary Metabolites from the Latex of Croton lechleri (Muell-Arg) and Evaluation of Their Antioxidant Activity Simona De Marino, Fulvio Gala, Franco Zollo, Sara Vitalini, Gelsomina Fico, Francesco Visioli and Maria Iorizzi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Compound 2a C20H26O7 ÏàËÆ¶È:100% Journal of Natural Medicines 2009 63 408-414 Lignan and neolignan glucosides, and tachioside 2¡ä-O-4¡å-O-methylgallate from the leaves of Glochidion rubrum Wen-Hu Cai, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato and Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 1a ÏàËÆ¶È:95% Phytochemistry 2008 69 788-795 Neolignan glycosides from Symplocos caudata Changhong Huo, Hong Liang, Yuying Zhao, Bin Wang, Qingying Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 2a ÏàËÆ¶È:95% Phytochemistry 2008 69 788-795 Neolignan glycosides from Symplocos caudata Changhong Huo, Hong Liang, Yuying Zhao, Bin Wang, Qingying Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 7S,8S-threo-4,7,9,9'-Tetrahydroxy-3,3'-dimethoxy-8-O-4'-neolignan ÏàËÆ¶È:95% Archives of Pharmacal Research 2011 Vol 34, No 8 1289-1296 Phenolic Constituents of Acorus gramineus Cheol Hyeong Park, Ki Hyun Kim, Il Kyun Lee, Seung Young Lee, Sang Un Choi, Jei Hyun Lee, and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Compound 3a C20H26O7 ÏàËÆ¶È:95% Journal of Natural Medicines 2009 63 408-414 Lignan and neolignan glucosides, and tachioside 2¡ä-O-4¡å-O-methylgallate from the leaves of Glochidion rubrum Wen-Hu Cai, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato and Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (7R,8S)-1-(3,4-Dimethoxyphenyl)-2-O-(2-methoxy-4-omegahydroxypropylphenyl)propane-1,3-diol C21H28O7 ÏàËÆ¶È:90.4% Journal of Asian Natural products Research 2010 12 874-878 Two new 8-O-4¡ä-type lignans from the stem of Schima superba and their cell growth inhibitory activities against human cancer cell lines Wen Xu; Hui Wang; Guang-Xiong Zhou; Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (7S,8R)-1-(3,4-Dimethoxyphenyl)-2-O-(2-methoxy-4-omegahydroxypropylphenyl)propane-1,3-diol C21H28O7 ÏàËÆ¶È:90.4% Bulletin of the Korean Chemical Society 2005 26 913-915 Lignans from the Flower Buds of Magnolia fargesii Jun Lee, Min Suk Yang, Sang Hae Nam, Mi Yae Shon, Seon Woo Hwang, Ki Hun Park* Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-methoxy-8,4'-oxyneoligna-3',4,7,9,9'-pentol C19H24O7 ÏàËÆ¶È:90% Phytochemistry 1992 31 3659-3661 Lignans from leaves of Juniperus chinensis Fang Jim-Min, Lee Ching-Kuo, Cheng Yu-Shia Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 7S,8R-erythro-4,7,9,9'-Tetrahydroxy-3,3'-dimethoxy-8-O-4'-neolignan ÏàËÆ¶È:90% Archives of Pharmacal Research 2011 Vol 34, No 8 1289-1296 Phenolic Constituents of Acorus gramineus Cheol Hyeong Park, Ki Hyun Kim, Il Kyun Lee, Seung Young Lee, Sang Un Choi, Jei Hyun Lee, and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 1-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]-propane-1,3-diol C20H26O7 ÏàËÆ¶È:90% Magnetic Resonance in Chemistry 2006 44 633-636 Lignans from the bark extract of Pinus sylvestris L. (pages 633¨C636) Jari Sinkkonen, Maarit Karonen, Jaana Liimatainen and Kalevi Pihlaja Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-(3,4-dimethoxy phenyl)-2-O-(2-methoxy-4-omegahydroxy propylphenyl)propane-1,3-diol ÏàËÆ¶È:90% Natural Product Research and Development 2010 22 945-948 Lignans from the Stem of Schima superba XU Wen; ZHOU Guang-xiong; YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (1S,3R)-1-(3,4-dimethoxy-phenyl)-2-[4-(3-hydroxy-propyl)-2-methoxy-phenoxy]-propane-1,3-diol ÏàËÆ¶È:90% Chinese Traditional and Herbal Drugs 2013 44 1397-1399 Chemical constituents from flower buds of She Medicine Magnolia liliflora LIU Ting-ting, WU Hai-bo, WANG Wen-shu, LAN Xiao-cong Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Ligraminol E C20H26O6 ÏàËÆ¶È:85% Journal of Natural Products 2011 74 2187-2192 Bioactive Lignans from the Rhizomes of Acorus gramineus Ki Hyun Kim, Ho Kyung Kim, Sang Un Choi, Eunjung Moon, Sun Yeou Kim, and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 11b ÏàËÆ¶È:85% Chemical & Pharmaceutical Bulletin 1987 35 3713-3719 Studies on the Glycosides of Epimedium grandiflorum MORR. var. thunbergianum (MIQ.) NAKAI. II TOSHIO MIYASE,AKIRA UENO,NOBUO TAKIZAWA,HIROMI KOBAYASHI and HIROKO OGUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 1-(4-hydroxy-3-methoxyphenyl)-2-[-4-(-hydroxypropyl-2-methoxy)-phenoxyl]-propane-1,3-diol C20H26O7 ÏàËÆ¶È:85% Natural Product Research and Development 2013 25 36-39 Study on Chemical Components From Leaves of Mangifera indica L. GU Cheng-zhen, LIU Fei-fei, YAO Yuan-cheng, LIU lu, CAO Jian-xin Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3,3'-dimethoxy-4,8'-oxyneoligna-9,4',7',9'-tetraol ÏàËÆ¶È:85% Chinese Traditional and Herbal Drugs 2012 43 1057-1060 Chemical constituents of Acanthopanax senticosus and their free radical scavenging activities ZHANG Tao; PIAO Jun-hong; YUAN Lei; LI Xi-feng; Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Ligraminol D C21H28O6 ÏàËÆ¶È:80.9% Journal of Natural Products 2011 74 2187-2192 Bioactive Lignans from the Rhizomes of Acorus gramineus Ki Hyun Kim, Ho Kyung Kim, Sang Un Choi, Eunjung Moon, Sun Yeou Kim, and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Compound 1 ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry 2008 16 2645-2650 Low molecular weight lignin suppresses activation of NF-¦ÊB and HIV-1 promoter Shinya Mitsuhashi, Takao Kishimoto, Yasumitsu Uraki, Takashi Okamoto, Makoto Ubukata Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (7'R,8'R)-2,2'-Dimethoxy-4-(3-hydroxyl-propenyl)-4'-(1,2,3-trihydroxy-propyl) biphenyl ether ÏàËÆ¶È:80% Archives of Pharmacal Research 2007 30 1067-1074 Lignan and terpene constituents from the aerial parts of saussurea pulchella Sang Un Choi, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (-)-(7S,8R)-dihydrodehydrodiconiferyalcohol C20H24O6 ÏàËÆ¶È:80% Acta Botanica Yunnanica 2010 32 83-86 A New Phenolic Glycoside from Chloranthusmul tistachys (Chloranthaceae) RAN Xin-Hui, N I Wei, WEI Gang, CHEN Chang-Xiang, LIU Hai-Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . erythro-1-(4-hydroxy-3-methoxyphenyl)-2-[2-hydro-xy-4-(3-hydroxypropyl) phenoxy]-1,3-propanediol C19H24O7 ÏàËÆ¶È:80% Chinese Journal of Natural Medicines 2011 9 26-29 Five Lignans and an Iridoid from Sambucus williamsii OUYANG Fu, LIU Yuan, LI Rong, LI Ling, WANG Nai-Li, *, YAO Xin-Sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . threoguaiacylglycerol-¦Â-O-4'-dihydroconiferyl ether ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2012 43 649-652 Chemical constituents from barks of Ailanthus altissima WANG Yan; ZHANG Hai-ning; WANG Wen-jing; ZHANG Sheng-yuan; ZHANG Xiao-qi; YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . erythro-1-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]-1,3-propanediol ÏàËÆ¶È:80% Journal of Shenyang Pharmaceutical University 2012 29 9-11 Isolation and identification of chemical constituents from seeds of Crataegus pinnatifida Bge. ZHAO Lei; LI Ling-zhi; PENG Ying; SONG Shao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ËÕʽ-Óú´´Ä¾»ù¸ÊÓÍ-¦Â-O-4'-ËɰػùÃÑ ÏàËÆ¶È:80% China Journal of Chinese Materia Medica 2012 37 1968-1972 Lignans from Sinocalamus affinis ZHU Mei; XIONG Liang; WANG Yanan; CHEN Minghua; JIANG Bingya; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . ³àʽ-Óú´´Ä¾»ù¸ÊÓÍ-¦Â-O-4'-ËɰػùÃÑ ÏàËÆ¶È:80% China Journal of Chinese Materia Medica 2012 37 1968-1972 Lignans from Sinocalamus affinis ZHU Mei; XIONG Liang; WANG Yanan; CHEN Minghua; JIANG Bingya; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . chushizisin C C19H24O6 ÏàËÆ¶È:75% Journal of Natural Products 2009 72 621-625 Antioxidant Lignans from the Fruits of Broussonetia papyrifera Ren-Qiang Mei, Yue-Hu Wang, Guan-Hua Du, Guang-Ming Liu, Li Zhang, and Yong-Xian Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 1-(4'-hydroxy-3'-methoxyphenyl)-2-[4''-(3-hydroxypropyl)-2'',6''-dimethoxyphenoxy]propane-1,3-diol ÏàËÆ¶È:75% Phytochemistry 2005 66 2745-2751 Bioactive constituents from roots of Bursera tonkinensis Aranya Jutiviboonsuk, Hongjie Zhang, Ghee Teng Tan, Cuiying Ma,Nguyen Van Hung, Nguyen Manh Cuong, Nuntavan Bunyapraphatsara,D. Doel Soejarto, Harry H.S. Fong Structure 13C NMR ̼Æ×Ä£Äâͼ |
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