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54.31,54.31,56.35,56.35,56.35,56.35,71.77,71.77,86.04,86.04,102.66,102.66,102.66,102.66,132.05,132.05,134.26,134.26,147.12,147.12,147.12,147.12.
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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