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ÕæÒ¹Mayoͳæ (³õÈëÎÄ̳)
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| 33.24, 35.74, 44.90, 46.80, 56.53, 56.54, 63.66, 65.76, 112.57, 115.44, 115.61, 117.27, 124.18, 128.63, 133.27, 136.15, 145.70, 146.00, 148.00,148.42 |
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²éѯ½á¹û£º¹²²éµ½725¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . burselignan C20H24O6 ÏàËÆ¶È:100% 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 -------------------------------------------------------------------------------- 2 . burselignan ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2009 34 1225-1227 Lignans from stems of Sambucus williamsii OUY ANG Fu, LIU Yuan, XI AO Huihui, YU Haiyang, WANG Naili, YAO Xinsheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . sodium (+)-isolaricireinol-2a-sulfate C20H23O9S ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 2002 50(5) 605-608 Constituents from Polygonum cuspidatum Kai XIAO, Lijiang XUAN, Yaming XU, Donglu BAI, and Dexin ZHONG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (+)-isolariciresinol ÏàËÆ¶È:75% Journal of Ethnopharmacology 2008 117 249-256 Anti-HIV-1 activities of compounds isolated from the medicinal plant Rhus chinensis Rui-Rui Wang, Qiong Gu, Yun-Hua Wang, Xue-Mei Zhang, Liu-Meng Yang, Jun Zhou, Ji-Jun Chen, Yong-Tang Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . negundin B C20H22O6 ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 2004 52(11) 1269-1272 Enzymes Inhibiting Lignans from Vitex negundo AZHAR-UL-HAQ, Abdul MALIK,Itrat ANIS, Sher Bahadar KHAN, Ejaz AHMED, Zaheer AHMED,Sarfraz Ahmad NAWAZ, and Muhammad Iqbal CHOUDHARY Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (+)-isolariciresinol ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 7 . isolariciresinol ÏàËÆ¶È:70% China Journal of Chinese Materia Medica 2009 34 1225-1227 Lignans from stems of Sambucus williamsii OUY ANG Fu, LIU Yuan, XI AO Huihui, YU Haiyang, WANG Naili, YAO Xinsheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (+)-isolariciresinol ÏàËÆ¶È:70% China Journal of Chinese Materia Medica 2007 32 688-691 Studies on chemical constituents in root of Isatis indigotica ZUO Li, LI Jianbei, XU Jing, YANG Jingzhi, ZHANG Dongming, TONG Yongling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . isolariciresinol ÏàËÆ¶È:70% China Journal of Chinese Materia Medica 2006 31 1696-1699 Studies on chemical constituents from root of Clematis hexapetala DONG Caixia, SHI Shepo, WU Kesi, TU Pengfei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . isolariciresinol ÏàËÆ¶È:70% Acta Pharmaceutica Sinica 2003 Vol 38 520-522 Studies on the lignans from Patrinia scabra LI Ting-zhao; ZHANG Wei-dong; GU Zheng-bing; LIU Wen-yong; ZHOU Jing; CHEN Wan-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound A C20H24O6 ÏàËÆ¶È:70% Archives of Pharmacal Research 1990 13 289-291 A lignan from Rubia akane Byung Hoon Han, Man Ki Park and Yeon-Hwa Park Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Isolariciresinol C17H26O10 ÏàËÆ¶È:70% Chemistry of Natural Compounds 2010 46 459-461 Chemical investigation of Ervatamia yunnanensis Jing-Ling Du, Yong-Sheng Jin, Li-Ming Qiao, Li Jin and Hai-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . isolariciresinol ÏàËÆ¶È:70% Chinese Pharmaceutical Journal 2009 44 490-492 Studies on Chemical Constituents in Forsythia suspensa (Thunb.) Vahl FENG Wei-sheng, LI Ke-ke, ZHENG Xiao-ke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . ÒìÂäÒ¶ËÉÖ¬´¼ ÏàËÆ¶È:70% Chinese Pharmaceutical Journal 2010 45 650-653 Study on Lignans from Catunaregam spinosa GAO Guang-chun, TAO Shu-hong, ZHANG Si, LI Qing-xin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (7S,8S)-1-(4-Hydroxy-3-methoxyphenyl)-2-O-(6-hydroxy-2-methoxy-4-omegahydroxypropylphenyl)propane-1,3-diol C20H26O8 ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 16 . isolariciresinol ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 17 . (+)-isolariciresinol ÏàËÆ¶È:70% 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 -------------------------------------------------------------------------------- 18 . (+)-isolariciresinol C20H24O6 ÏàËÆ¶È:70% Archives of Pharmacal Research 2012 35 1739-1747 Phenylpropanoids and Lignanoids from Euonymus acanthocarpus Jia Xian Zhu, Jie Ren, Jiang Jiang Qin, Xiang Rong Cheng, Qi Zeng, Fei Zhang, Shi Kai Yan, Hui Zi Jin,and Wei Dong Zhang, Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . isotaxiresinol 4-O-methyl ether ÏàËÆ¶È:70% Acta Pharmaceutica Sinica 2011 46 179-182 A new ¦Â-naphthalenecarboxylic acid biglycoside from Chirita longgangensis var. hongyao WANG Man-yuan, GONG Mu-xin, ZHANG Dong, YANG Lan* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . gaultherin A derivative C21H26O7 ÏàËÆ¶È:66.6% Phytochemistry 1999 51 469-472 Gaultherins A and B, two lignans from Gaultheria yunnanensis Zhizhen Zhang, Dean Guo, Changling Li, Junhua Zheng, Kazuo Koike, Zhonghua Jia, Tamotsu Nikaido Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . (+)-5'-methoxy-isolariciresinol ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2012 37 1227-1231 Chemical constituents from roots of Machilus yaoshansis LIU Bo; LIU Mingtao; GAN Maoluo; ZHAO Feng; WU Xiuli; YU Yang; YUE Zhenggang; LIN Sheng; WANG Sujuan; ZHU Chenggen; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . shogasulfonic acid B C20H25O8S ÏàËÆ¶È:65% Phytochemistry 2003 613-617 Pharmacognostic studies on ginger and related drugs¡ªpart 1:five sulfonated compounds from Zingiberis rhizome (Shokyo) Yumiko Hori, Tsuyoshi Miura, Yasuaki Hirai, Motonori Fukumura,Yukio Nemoto, Kazuo Toriizuka, Yoshiteru Ida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . compound 3 ÏàËÆ¶È:65% Journal of Natural Products 1998 61 1137-1139 Isolation and Absolute Structures of Enantiomeric 1, 2-Bis(4-hydroxy-3-methoxyphenyl)-1, 3-propanediol 1-O-Glucosides from the Bark of Hovenia trichocarpa Kazuko Yoshikawa, Noriko Mimura, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . hydroxymatairesinol C20H22O7 ÏàËÆ¶È:65% Molecules 2006 11 103-114 Screening Analyses of Pinosylvin Stilbenes, Resin Acids and Lignans in Norwegian Conifers Hanne Hovelstad, Ingebjorg Leirset, Karin Oyaas and Anne Fiksdahl Structure 13C NMR ̼Æ×Ä£Äâͼ |
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