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²éѯ½á¹û£º¹²²éµ½115¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (-)-syringaresinol C22H26O8 ÏàËÆ¶È:90.9% Korean Journal of Pharmacognosy 2000 31(3) 357-363 Phytochemical Constituents of Actinidia arguta Whang, Joon-Ih; Zee, Ok-Pyo; Moon, Hyung-In Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . syringaresinol ÏàËÆ¶È:86.3% Journal of Asian Natural Products Research 2001 3 95-102 Two New Germacranolides from Magnolia Grandiflora SHAO-HUA WU, XIAO-DONG LUO, YUN-BAO MA,XIAO-JIANG HAO, JUN ZHOU and DA-GANG WU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (Ê¿)-¶¡ÏãÊ÷Ö¬´¼ ÏàËÆ¶È:86.3% Chinese Traditional and Herbal Drugs 2006 37 345-347 ºÚÁú¹Ç»¯Ñ§³É·ÖµÄÑо¿ ÕÅÔ®»¢;ÑîÑÇæÃ;³Â¶«ÁÖ;Íõ·æÅô Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (+)-syringaresinol ÏàËÆ¶È:86.3% Archives of Pharmacal Research 1999 22 417-422 Two new lignans from Lindera obtusiloba blume Hak Cheol Kwon, Sang Un Choi, Jung Ock Lee, Ki Hwan Bae and Ok Pyo Zee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (+)-Syringaresinol ÏàËÆ¶È:86.3% Archives of Pharmacal Research 2006 29 203-208 Cytotoxic terpenes and lignans from the roots of Ainsliaea acerifolia Sang Zin Choi, Min Cheol Yang, Sang Un Choi and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (+)-syringaresinol ÏàËÆ¶È:86.3% Journal of the Chinese Chemical Society 1998 45 629-634 Lignans and Kauranes from the Stems of Annona cherimola ê?ÖÐÒ»(Chung-Yi Chen);…Ç–|·f(Tung-Ying Wu);?ˆ·¼˜s(Fang-Rong Chang);…ÇÓÀ²ý(Yang-Chang Wu) Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (-) syringaresinol ÏàËÆ¶È:86.3% Journal of Peking University (Health Sciences) 2003 35 180-183 Isolation and identification of chemical constituents from Albizia julibrissin Durazz TONG Wenyong; MI Liang; LIANG Hong; ZHAO Yuying Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (+)-Syringaresinol ÏàËÆ¶È:86.3% Chinese Journal of Applied & Environmental Biology 2006 12 163-169 Chemical Constituents from Gymnosporia varialilis Loes. ZHANG Xiuyun; LI Bogang; ZHOU Min; YUAN Xiaohong; & ZHANG Guolin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . De-4''-O-methylmagnolin ÏàËÆ¶È:81.8% Phytochemistry 1993 32 1421-1424 Biotransformation of (+)-magnolin and (+)-yangabin in rat Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . De-4'-O-methylyangabin ÏàËÆ¶È:78.2% Phytochemistry 1993 32 1421-1424 Biotransformation of (+)-magnolin and (+)-yangabin in rat Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (1R,2S,5R,6S)-2-(3,4-methylenedioxyphenyl)-6-(4-hydroxy-3,5-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane C21H22O7 ÏàËÆ¶È:77.2% Journal of Natural Products 2007 70 544-548 Bioactive Lignans from Peperomia duclouxii Na Li,Jian-lin Wu,Toshiaki Hasegawa, Jun-ichi Sakai,Li-ming Bai,Li-yan Wang, Saori Kakuta, Yumiko Furuya, Hirotsugu Ogura,Takao Kataoka,Akihiro Tomida,Takashi Tsuruo,and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3,3'-bis(3,4-dihydro-4-hydroxy-6,8-dimethoxy-2H-1-benzopyran) C22H26O8 ÏàËÆ¶È:77.2% Natural Product Research 2008 22 915-920 Bisbenzopyrans and alkaloids from the roots of Stemona cochinchinensis Pham-Huu Dien; Li-Gin Lin; Chun-Ping Tang; Chang-Qiang Ke; Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (+)-De-4"-O-methylmagnolin C22H26O7 ÏàËÆ¶È:77.2% Phytochemistry 1995 39 1027-1030 Biotransformation of lignans: Metabolism of (+)-eudesmin and (+)-magnolin in Spodoptera litura Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Medioresinol ÏàËÆ¶È:77.2% Guihaia 2013 33 191-194 Study on phenylpropanoids from hypocotyls of the mangrove plant Bruguiera gymnorrhiza YI Xiang-Xi, GAO Cheng-Hai*, HE Bi-Juan, CHEN Bo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (¡À)-buddlenol D ÏàËÆ¶È:73.0% Natural Product Research and Development 2003 15 277-283 STUDIES ON THE PHENYLPROPANOIDS FROM CARAGANA ROSEA CUI Yi-ling; MU Qing; HU Chang-qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (1S,2R,5S,6R)-2-(5-methoxy-3,4-methylenedioxyphenyl)-6-(4-hydroxy-3,5-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane C22H24O8 ÏàËÆ¶È:72.7% Journal of Natural Products 2007 70 544-548 Bioactive Lignans from Peperomia duclouxii Na Li,Jian-lin Wu,Toshiaki Hasegawa, Jun-ichi Sakai,Li-ming Bai,Li-yan Wang, Saori Kakuta, Yumiko Furuya, Hirotsugu Ogura,Takao Kataoka,Akihiro Tomida,Takashi Tsuruo,and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (+)-medioresinol C21H24O7 ÏàËÆ¶È:72.7% Korean Journal of Pharmacognosy 2000 31(3) 357-363 Phytochemical Constituents of Actinidia arguta Whang, Joon-Ih; Zee, Ok-Pyo; Moon, Hyung-In Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (+)-medioresinol ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 2010 35 1261-1271 Chemical constituents of stems and branches of Adina polycephala ZHANG Yanling; GAN Maoluo; LI Shuai; WANG Sujuan; ZHU Chenggen; YANG Yongchun; HU Jinfeng; CHEN Naihong; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (-)-syringaresinol-4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:72.7% Pharmacy and Pharmacology Communications 1997 3 525-527 Lignans from Eleutherococcus senticosus (Siberian Ginseng) TATYANA N. MAKARIEVA, ANDREY S. DMITRENOK, VALENTIN A. STONIK, ASMITA V. PATEL and LESLEY M. CANFIELD Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 5'-medioresinol C21H24O7 ÏàËÆ¶È:72.7% Chinese Traditional and Herbal Drugs 2013 44 2358-2363 Chemical constituents from barks of Cinnamomum cassia growing in China ZHAO Kai, YIANG Yong, XUE Pei-feng, TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . viscoloratin C27H32O13 ÏàËÆ¶È:69.2% Asian Journal of Traditional Medicines 2007 2 58-60 A New Tetrahydrofuran Lignan Glycoside from Viscum coloratum Jun Yin , Xiaokang Wang , Zhihui Liu and Shigetoshi Kadota Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . medioresinol ÏàËÆ¶È:68.1% Journal of Asian Natural Products Research 2001 3 95-102 Two New Germacranolides from Magnolia Grandiflora SHAO-HUA WU, XIAO-DONG LUO, YUN-BAO MA,XIAO-JIANG HAO, JUN ZHOU and DA-GANG WU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . (+)-epi-syringaresinol C22H26O8 ÏàËÆ¶È:68.1% Journal of the Chinese Chemical Society 1998 45 629-634 Lignans and Kauranes from the Stems of Annona cherimola ê?ÖÐÒ»(Chung-Yi Chen);…Ç–|·f(Tung-Ying Wu);?ˆ·¼˜s(Fang-Rong Chang);…ÇÓÀ²ý(Yang-Chang Wu) Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . (+)-Medioresinol ÏàËÆ¶È:68.1% Journal of Chinese Pharmaceutical Sciences 2013 22 431-434 Chemical constituents from the leaves of Premna microphylla Turcz Zhengxi Hu, Yongbo Xue, Guangmin Yao, Zengwei Luo, Yanyan Wang*, Yonghui Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . (¡À)-buddlenol C ÏàËÆ¶È:65.3% Natural Product Research and Development 2003 15 277-283 STUDIES ON THE PHENYLPROPANOIDS FROM CARAGANA ROSEA CUI Yi-ling; MU Qing; HU Chang-qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . (1R,2S,5R,6R)-6-(3-ethyl-4-hydroxy-5-methoxyphenyl)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]-octane C23H28O7 ÏàËÆ¶È:63.6% Helvetica Chimica Acta 2001 Vol. 84 157 A Lignoid Glycoside and Dimeric Phenylpropanoids from Daphne oleoides Nisar Ullah, Prinz Sonja,Ernst Haslinger,Wagar Ahmed ,Mohammed Arfan and Abdul Malik Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . De-4'-O-methylmagnolin ÏàËÆ¶È:63.6% Phytochemistry 1993 32 1421-1424 Biotransformation of (+)-magnolin and (+)-yangabin in rat Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . de-4'-O-methyl-5'-hydroxymagnolin C22H26O8 ÏàËÆ¶È:63.6% Phytochemistry 1993 34 1501-1507 Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . (+)-medioresinol C21H24O7 ÏàËÆ¶È:63.6% Korean Journal of Pharmacognosy 2004 35(3) 194-198 Phytochemical Constituents of the Root Bark from Albizzia julibrissin Durazz Go, Jae-Jong; Woo, Eun-Rhan; Moon, Young-Hee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . medioresinol ÏàËÆ¶È:63.6% Chinese Traditional and Herbal Drugs 2006 37 672-673 °×Âí¹ÇÒ¶µÄ»¯Ñ§³É·ÖÑо¿ ÕÅÇ¿;Ëï¡Èå Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . medioresinol ÏàËÆ¶È:63.6% Chinese Pharmaceutical Journal 2008 43 1066-1069 Studies on Chemical Constituents in Fruit of Melia toosendan XIE Fan, ZHANG mian, ZHANG Chao-feng, WANG Zheng-tao, YU Bo-yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . medioresinol C21H24O7 ÏàËÆ¶È:63.6% Bioscience, Biotechnology, and Biochemistry 1996 60 1714-1716 Antioxidative Compounds Isolated from Kokuto, Non-centrifugal Cane Sugar Yoko NAKASONE, Kensaku TAKARA, Kouji WADA, Junichi TANAKA, Seiichi YOGI, Nobuji NAKATANI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . (+)-medioresinol ÏàËÆ¶È:63.6% Natural Product Research and Development 2007 19 55-58 Chemical Constituents of Daphne tangutica YUAN Xiao-hong;XU Chun-xia; ZHOU Min; ZHANG Xiu-yun; LI Bo-gang * Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . Medioresinol ÏàËÆ¶È:63.6% Journal of Chinese Pharmaceutical Sciences 2010 19 95-99 Chemical ingredients isolated from the aerial parts of Artemisia anomala Ke Zan; Xiao-Qing Chen; Qiang Fu; Si-Xiang Zhou; Mei-Tian Xiao; Jing Wen; Peng-Fei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . (+)-medioresinol ÏàËÆ¶È:63.6% Chinese Journal of Natural Medicines 2012 10 32-35 Chemical constituents of Spatholobus suberectus Ren-Neng TANG, Xiao-Bo QU, Shu-Hong GUAN, Ping-Ping XU, Yang-Yang SHI, De-An GUO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . (+)-Medioresinol ÏàËÆ¶È:63.6% Natural Product Research and Development 2012 24 469-472 Phenylpropanoids from Roots of Acanthopanax sessiliflorus(Rupr.et Maxim.) Seem. YU Kai; SONG Yang; LU Yang; XIONG Zhi-li; LI Fa-mei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . (-)-medioresinol ÏàËÆ¶È:63.6% Chinese Traditional and Herbal Drugs 2012 43 2351-2355 Study on chemical constituents of Eupatorium odoratum WANG Yun; SIMA Shuo-dan; LI Ji-xia; ZHAO Ting; LI Zhi; WANG Yu-fang; ZHANG Man-li; SHI Qing-wen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . (+)-ÂóµÏ°ÂÖ¬ËØ ÏàËÆ¶È:63.6% Journal of Chinese Medicinal Materials 2006 29 786-788 Studies on Chemical Constituents of Serissa serissoides Roots ZHANG Qiang, SUN Long-ru Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . (+)-ÂóµÏ°ÂÖ¬ËØ ÏàËÆ¶È:63.6% Journal of Chinese Medicinal Materials 2010 33 555-556 Studies on the Chemical Constituents of Solanum nigrum ZHAO Ying, LIU Fei, LOU Hong-xiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . (+)-magnolin ÏàËÆ¶È:60.8% Phytochemistry 1994 35 611-613 An insect growth inhibitory lignan from flower buds of Magnolia fargesii Mitsuo Miyazawa, Yukio Ishikawa, Hiroyuki Kasahara, Jun-ichi Yamanaka, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . threobuddlenol C ÏàËÆ¶È:60.8% China Journal of Chinese Materia Medica 2013 38 2826-2831 Chemical constituents from stems of Aquilaria sinensis LI Wei, MEI Wen-li, WANG Hao, ZUO Wen-jian, YANG De-lan, DAI Hao-fu, Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . erythro-buddlenol C ÏàËÆ¶È:60.8% China Journal of Chinese Materia Medica 2013 38 2826-2831 Chemical constituents from stems of Aquilaria sinensis LI Wei, MEI Wen-li, WANG Hao, ZUO Wen-jian, YANG De-lan, DAI Hao-fu, Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . di-erythro-syringylglycerol-¦Â-O-4,4'-syringaresinol ether C44H54O18 ÏàËÆ¶È:59.0% Chemistry & Biodiversity 2007 Vol. 4 118 Phytotoxicity of Secondary Metabolites from Aptenia cordifolia Marina DellaGreca, Antonio Fiorentino, Angelina Izzo, Filomena Napoli, Raffaella Purcaro, and Armando Zarrelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . (2S,3R,6S)-2-[hydroxy(4-hydroxy-3,5-dimethoxyphenyl)methyl]-3-(5-methoxy-3,4-methylenedioxybenzyl)butyrolactone C22H24O9 ÏàËÆ¶È:59.0% Journal of Natural Products 2006 69(2) 234-239 Bioactive Dibenzylbutyrolactone and Dibenzylbutanediol Lignans from Peperomia duclouxii Na Li, Jian-lin Wu, Toshiaki Hasegawa, Jun-ichi Sakai, Li-yan Wang, Saori Kakuta, Yumiko Furuya, Akihiro Tomida, Takashi Tsuruo, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . 8'-methoxy-3,3'-bis(3,4-dihydro-4-hydroxy-6-methoxy-2H-1-benzopyran) C21H24O7 ÏàËÆ¶È:59.0% Natural Product Research 2008 22 915-920 Bisbenzopyrans and alkaloids from the roots of Stemona cochinchinensis Pham-Huu Dien; Li-Gin Lin; Chun-Ping Tang; Chang-Qiang Ke; Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . (+)-medioresinol ÏàËÆ¶È:59.0% China Journal of Chinese Materia Medica 2009 34 2761-2764 Chemical constituents of Galium verum ZHAO Chunchao, SHAO Jianhua, CAO Dandan, ZHANG Yuwei LIXian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . medioresinol ÏàËÆ¶È:59.0% China Journal of Chinese Materia Medica 2008 33 409-411 Studies on chemical constituents of Heliciopsis lobata¢ò LI Dan, Liu Mingsheng, LI Zhanlin, KANG Shengli, HUA Huiming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . (+)-de-O-methyhnagnolin C22H26O7 ÏàËÆ¶È:59.0% Phytochemistry 1993 34 1501-1507 Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . (+)-de-O-methylmagnolin ÏàËÆ¶È:59.0% Phytochemistry 1992 31 3666-3668 Phenolic lignans from flower buds of Magnolia fargesii Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . fragransin B3 C22H28O7 ÏàËÆ¶È:59.0% Chemical & Pharmaceutical Bulletin 1987 35 3309-3314 New Phenylethanoid Glycosides from Cistanche tubulosa (SCHRENK) HOOK. f. I. HIROMI KOBAYASHI,HIROKO OGUCHI,NOBUO TAKIZAWA,TOSHIO MIYASE,AKIRA UENO,KHAN USMANGHANI and MANSOOR AHMAD Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 51 . (+)-medioresinol C21H24O7 ÏàËÆ¶È:59.0% Chinese Journal of Natural Medicines 2006 4 198-201 Chemical Constituents from Serissa serissoides WANG Min; LIANG Jing-Yu; LIU Xue-Ting; QIU Wen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 52 . Rayalinol 22H26O8 ÏàËÆ¶È:59.0% Tetrahedron 2010 66 1716-1720 A new lignan and a new sesquiterpene from Eurotia ceratoides (L.) Bina Shaheen Siddiqui, Kalamkas Zhanarbekovna Butabayeva, Gauhar Shahmanovna Burasheva, Sobiya Perwaiz, Syed Kashif Ali, Huma Aslam Bhatti Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 53 . aschantin ÏàËÆ¶È:59.0% Journal of the Chinese Chemical Society 1998 45 773-778 The Constituents from the Leaves of Magnolia coco ÓÎåaéÅ(Hsi-Jung Yu);ê?½¨Ö¾(Chien-Chih Chen);Öx²©ßM(Bor-Jinn Shieh) Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 54 . syringaresinol 4-O-¦Â-D-glucopyranoside C28H36O13 ÏàËÆ¶È:59.0% Chinese Journal of Pharmaceuticals 2007 38 221-226 Two New Compounds from Picrorhiza scrophulariiflora XIE Zhi-yong, HU Hong-xia, KONG De-yun, YANG Pei-ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 55 . syringaresinol ÏàËÆ¶È:59.0% China Journal of Chinese Materia Medica 2011 36 1969-1974 Chemical constituents of Excoecaria acerifclia HU, Jiang, ZHANG, Lanchun, ZHAO, Qinshi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 56 . (+)-yangabin ÏàËÆ¶È:58.3% Phytochemistry 1993 32 1421-1424 Biotransformation of (+)-magnolin and (+)-yangabin in rat Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 57 . (+)-yangabin ÏàËÆ¶È:58.3% Phytochemistry 1993 34 1501-1507 Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 58 . (+)-(7¦Á,7'¦Á,8¦Á,8'¦Á)-3',4,4',5,5'-pentamethoxy-7,9':7',9-diepoxylignan-3-ol C23H28O8 ÏàËÆ¶È:56.5% Helvetica Chimica Acta 2008 Vol. 91 2361 Lignans from the Bark of Magnolia kobus Hak-Ju Lee, Seon-Mi Seo, Oh-Kyu Lee, Hyun-Jin Jo, Ha-Young Kang, Don-Ha Choi, Ki-Hyon Paik, and Merajuddin Khan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 59 . (+)-Magnolin ÏàËÆ¶È:56.5% Phytochemistry 1995 39 1027-1030 Biotransformation of lignans: Metabolism of (+)-eudesmin and (+)-magnolin in Spodoptera litura Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 60 . (+)-magnolin ÏàËÆ¶È:56.5% Phytochemistry 1993 32 1421-1424 Biotransformation of (+)-magnolin and (+)-yangabin in rat Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 61 . (+)-magnolin ÏàËÆ¶È:56.5% Phytochemistry 1993 34 1501-1507 Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 62 . (+)-(7¦Á,7'¦Á,8¦Á,8'¦Á)- 4,5-dimethoxy-3',4'-(methylenedioxy)-7,9': 7',9-diepoxylignan-3-ol C21H22O7 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2008 Vol. 91 2361 Lignans from the Bark of Magnolia kobus Hak-Ju Lee, Seon-Mi Seo, Oh-Kyu Lee, Hyun-Jin Jo, Ha-Young Kang, Don-Ha Choi, Ki-Hyon Paik, and Merajuddin Khan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 63 . (+)-pinoresinol ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2004 52(10) 1265-1267 A New Lignan from Balanophora abbreviata and Inhibition of Lipopolysaccharide (LPS)-induced Inducible Nitric Oxide Synthase(iNOS) Expression Akihiro HOSOKAWA,Megumi SUMINO, Tomonori NAKAMURA,Shingo YANO, Toshikazu SEKINE,Nijsiri RUANGRUNGSI, Kazuko WATANABE,and Fumio IKEGAMI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 64 . sesamin ÏàËÆ¶È:54.5% Phytochemistry 2002 61 963-966 A lignan from the root of Ecbolium linneanum Kurz. R. Venkataraman, S. Gopalakrishnan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 65 . (1S,2R,5S,6R)-2-(5-methoxy-3,4-methylenedioxyphenyl)-6-(3,4-dihydroxy-5-methoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane C21H22O8 ÏàËÆ¶È:54.5% Journal of Natural Products 2007 70 544-548 Bioactive Lignans from Peperomia duclouxii Na Li,Jian-lin Wu,Toshiaki Hasegawa, Jun-ichi Sakai,Li-ming Bai,Li-yan Wang, Saori Kakuta, Yumiko Furuya, Hirotsugu Ogura,Takao Kataoka,Akihiro Tomida,Takashi Tsuruo,and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 66 . (+)-2¦Á-(3',4'-dimethoxyphenyl)-6¦Á-(3''-hydroxy-4'',5''-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane C22H26O7 ÏàËÆ¶È:54.5% Chemistry of Natural Compounds 2008 44 419-421 FUROFURAN LIGNANS FROM THE BARK OF Magnolia kobus Seon-Mi Seo, Hak-Ju Lee, Oh-Kyu Lee,Hyun-Jin Jo, Ha-Young Kang, Don-Ha Choi,Ki-Hyon Paik, and M. Khan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 67 . Nobilin C C19H24O6 ÏàËÆ¶È:54.5% Journal of Asian Natural Products Research 2006 8 113-118 Three new bibenzyl derivatives from Dendrobium nobile XUE ZHANG, HAO GAO, NAI-LI WANG and XIN-SHENG YAO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 68 . aschantin ÏàËÆ¶È:54.5% China Journal of Chinese Materia Medica 1995 20 102-104 Biolgically Active Lignins from Magnolia bilndii Pamp Ma Yuliang and Han Guiqiu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 69 . (+)-Eudesmin ÏàËÆ¶È:54.5% Phytochemistry 1995 39 1027-1030 Biotransformation of lignans: Metabolism of (+)-eudesmin and (+)-magnolin in Spodoptera litura Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 70 . (+)-De-4'-O-methyleudesmin C21H24O6 ÏàËÆ¶È:54.5% Phytochemistry 1995 39 1027-1030 Biotransformation of lignans: Metabolism of (+)-eudesmin and (+)-magnolin in Spodoptera litura Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 71 . (+)-De-4',4"-O-dimethylepimagnolin A C21H24O7 ÏàËÆ¶È:54.5% Phytochemistry 1994 35 1191-1193 Microbial oxidation of (+)-epimagnolin a by Aspergillus niger Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 72 . (+)-eudesmin ÏàËÆ¶È:54.5% Phytochemistry 1993 34 1501-1507 Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 73 . (+)-de-4'-O-methyleudesmin C21H24O6 ÏàËÆ¶È:54.5% Phytochemistry 1993 34 1501-1507 Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 74 . (+)-pinoresinol C20H22O6 ÏàËÆ¶È:54.5% Phytochemistry 1993 34 1501-1507 Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 75 . (+)-magnolin ÏàËÆ¶È:54.5% Phytochemistry 1992 31 3666-3668 Phenolic lignans from flower buds of Magnolia fargesii Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 76 . kobusin ÏàËÆ¶È:54.5% Korean Journal of Pharmacognosy 2009 40(4) 315-318 Lignans from the Fruit of Magnolia denudata Yang, Seok-Won; Park, Sae-Rom; Lee, Hyun-Jin; Yang, Jae-Heon; Chae, Byeong-Suk; Kim, Hee-Ja; Kim, Dae-Keun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 77 . (1R,2S,5R,6R)-5'-O-methylpluviatilol C21H22O7 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry Letters 2012 22 2527-2533 Anti-inflammatory and PPAR transactivational effects of secondary metabolites from the roots of Asarum sieboldii Tran Hong Quang,Nguyen Thi Thanh Ngan,Chau Van Minh,Phan Van Kiem ,Bui Huu Tai ,Nguyen Phuong Thao ,Seok Bean Song,Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 78 . (+)-Piperitol C20H20O6 ÏàËÆ¶È:54.5% Phytochemical Analysis 1994 5 233-238 Analysis of the fungicidal constituents from the bark of Ocotea usambarensis Engl. (Lauraceae) Christian Terreaux, Marc Maillard, Kurt Hostettmann, Gaetano Lodi and Etienne Hakizamungu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 79 . (+)-fraxiresinol ÏàËÆ¶È:54.5% Chinese Traditional and Herbal Drugs 2008 39 1132-1135 Studies on chemical constituents of Ilex pernyi XIE Guang-bo; ZHAO Ming-bo; WANG Xiao-jing; TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 80 . sesamin ÏàËÆ¶È:54.5% Chinese Traditional and Herbal Drugs 1998 29 577-579 Studies on the Chemical Constituents of the Seed of Chinese Dodder(Cuscuta chinensis) Wang Zhan and He Zhisheng (Shanghai Institute of Materia Medica; Chinese Academy of Sciences; Shanghai; ); Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 81 . de-O-methylmagnollin ÏàËÆ¶È:54.5% Journal of the Chinese Chemical Society 1998 45 773-778 The Constituents from the Leaves of Magnolia coco ÓÎåaéÅ(Hsi-Jung Yu);ê?½¨Ö¾(Chien-Chih Chen);Öx²©ßM(Bor-Jinn Shieh) Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 82 . piperitol ÏàËÆ¶È:54.5% The Journal of Antibiotics 1994 47 487-491 NEW METABOLITES, TETRAHYDROFURAN LIGNANS, PRODUCED BY Streptomyces sp. IT-44 YIN-MEI CHIUNG, HIDEO HAYASHI, HIROSHI MATSUMOTO, TOSHIO OTANI, KEN-ICHIRO YOSHIDA, MING-YU HUANG, RU-XIAN CHEN, JING-RONG LIU, MITSURU NAKAYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 83 . pinoresinol ÏàËÆ¶È:54.5% Heterocycles 1993 36 933-936 Structure of Novel Antioxidative Lignan Triglucoside Isolated from Sesame Seed Hirotaka Katsuzaki, Shunro Kawakishi, and Toshihiko Osawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 84 . (+)-Sesamin ÏàËÆ¶È:54.5% Natural Product Communications 2006 1 21-25 Lignans from the Stem of Cinnamomum camphora TJ Hsieh, CH Chen, WL Lo and CY Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 85 . Pseuderesinol C21H24O8 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2012 60 1125-1133 Lignans and Triterpenes from the Root of Pseuderanthemum carruthersii var. atropurpureum Thi Nga Vo, Phi Linh Nguyen, Lam Truong Tuong, Lawrence Michael Pratt, Phung Nguyen Vo, Kim Phi Phung Nguyen, Ngoc Suong Nguyen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 86 . Piperitol C20H20O6 ÏàËÆ¶È:54.5% Journal of Wood Science 2000 46 476-482 Lignans of Chamaecyparis obtusa Naohiro Takaku, Don-Ha Choi. Keigo Mikame, Tomoya Okunishi, Shiro Suzuki, Hideo Ohashi, Toshiaki Umezawa, Mikio Shimada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 87 . sesamin ÏàËÆ¶È:54.5% Asian Journal of Chemistry 2002 14 277-282 Isolation and Characterisation of a New Stereoisomeric Furofuran Type of Lignan from Ecbolium linneanum Kurz R. Venkataraman and S. Gopalakrishnan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 88 . L-sesamin C20H18NO6 ÏàËÆ¶È:54.5% Chinese Traditional and Herbal Drugs 2013 44 1546-1551 Antibacterial constituents from roots of Zanthoxylum nitidum YE Yu-shan, LIU Jia-wei, LIU Xiao-qiang, QIU Jun-xin, MIN Huan, ZHENG Run-sheng, XU Hui, LI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 89 . Magnolin C23H28O7 ÏàËÆ¶È:54.5% Natural Product Sciences 2013 19 160-165 Phytochemical Studies on Magnoliae Flos (I) Isolation of Lignans from the Flower Buds of Magnolia biondii† Dong Hwa Lee, Soon Youl Kwon, Mi Hee Woo, Je Hyun Lee, and Kun Ho Son, * Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 90 . phyllostadimer A C42H50O16 ÏàËÆ¶È:50% Phytochemistry 2003 991-996 Two lignan dimers from bamboo stems (Phyllostachys edulis) Ai Suga, Yoshihisa Takaishi, Satoru Goto,Tatsuo Munakata, Izumi Yamauchi, Kentaro Kogure Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 91 . (-)-pinoresinol C20H20O6 ÏàËÆ¶È:50% Planta Medica 1982 45 167-171 Constituents of Daphne tangutica Zhuang Lingen, 0. Seligmann, K. Jurcic und H. Wagner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 92 . (-)-pinoresinol ÏàËÆ¶È:50% Acta Botanica Yunnanica 2000 22(2) 225-233 Chemical Constituents from Balanophora harlandii TENG Rong-Wei,WANGDe-Zu,YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 93 . Nobilin B C18H22O6 ÏàËÆ¶È:50% Journal of Asian Natural Products Research 2006 8 113-118 Three new bibenzyl derivatives from Dendrobium nobile XUE ZHANG, HAO GAO, NAI-LI WANG and XIN-SHENG YAO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 94 . magnolin ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 1995 20 102-104 Biolgically Active Lignins from Magnolia bilndii Pamp Ma Yuliang and Han Guiqiu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 95 . 5-methoxysesamin ÏàËÆ¶È:50% Phytochemistry 1998 49 157-161 Lignans and Sesquiterpene Lactones from Artemisia Sieversiana and Inula Racemosa R.X.Tan,H.Q.Tang,J.Hu,B.Shuai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 96 . (1 R,2S,5R,6S)-2-(3,4,5-trimethoxyphenyl)-6-(4-hydroxy-3-methoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane ÏàËÆ¶È:50% Phytochemistry 1997 44 1133-1137 Sesquiterpene lactones and lignans from Artemisia arborescens J. Alberto Marco, Juan F. Sanz-Cervera, Vicente Garc¨ªa-Lliso, Joan Vall¨¨s-Xirau Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 97 . (+)-5,5'-Dimethoxylariciresinol C22H28O8 ÏàËÆ¶È:50% Natural Product Sciences 2005 11 170-173 Isolation and Structural Identification of Minor Constituents from Sasa borealis Jeong, Yeon-Hee; Nam, Joo-Won; Lee, Na-Youn; Seo, Eun-Kyoung; Kwon, Young-Joo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 98 . Demethylpiperitol C19H18O6 ÏàËÆ¶È:50% Phytochemistry 1995 40 1511-1513 Lignans from Apollonias barbujana Cirilo P¨¦rez, Luz N. Almonacid, Juan M. Trujillo, Antonio G. Gonz¨¢lez, Simeona J. Alonso, Eduardo Navarro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 99 . (+)-pinoresinol ÏàËÆ¶È:50% Phytochemistry 1992 31 3666-3668 Phenolic lignans from flower buds of Magnolia fargesii Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 100 . (+)-aschantin ÏàËÆ¶È:50% Korean Journal of Pharmacognosy 2004 35(2) 152-156 Isolation of Melanin Biosynthesis Inhibitory Compounds from the Flowers of Magnolia denudata Xu, Guang-Hua; Kim, Jeong-Ah; Park, Sung-Hee; Son, Ae-Ryang; Chang, Tae-Soo; Chang, Hyun-Wook; Chung, See-Ryun; Lee, Seung-Ho Structure 13C NMR ̼Æ×Ä£Äâͼ |
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