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9.36,12.00,13.99,43.43,47.57,51.03,56.10,56.12,56.14,60.80,60.86,85.02,86.00,88.51,102.84,102.89,103.00,136.22,136.68,137.34,137.41,137.99,138.80,153.08,153.24,153.29

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15.24,15.84,20.27,29.82,34.28,40.67,41.92,56.02,60.57,60.73,60.90,71.97,110.08,112.77,122.85,123.20,127.62,133.05,133.81,137.19,139.68,140.32,142.24,151.66,151.78,152.54
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1 .     (R-biar)-12-angeloyloxy-6,7,8,9-tetrahydro-1,2,3,13,14-pentamethoxy-7,8-dimethyl-7-dibenzo[a,c]cyclooctenol
C28H36O8     ÏàËÆ¶È:96.2%
Journal of Asian Natural Products Research          2012          14          159-164
Two new lignans from Celastrus flagellaris Rupr.
Xue-Mei Zhao, Fu-Jiang Guo, Yi-Ming Li & Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     angeloyl gomisin H
    ÏàËÆ¶È:92.8%
Natural Product Sciences          2006          12          134-137
Gomisin J with Protective Effect Against t-BHP-Induced Oxidative Damage in HT22 Cells from Schizandra chinensis
An, Ren-Bo; Oh, Seung-Hwan; Jeong, Gil-Saeng; Kim, Youn-Chul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     flagelignanin A
C28H36O8     ÏàËÆ¶È:92.3%
Journal of Nanjing Military Medical College          2001          21          221-224
Study on the chemical composition in Euonymus fortunei
QU Fa-lin, DING Qing long, ZHANG Han-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     gomisin T
C23H30O7     ÏàËÆ¶È:76.9%
Chemical & Pharmaceutical Bulletin          1988          36          3811-3815
Strophanthidin Glycosides from the Roots of Apocynum venetum var. : basikurumon : Studies on Apocynum. II
FUMIKO ABE,YJIRO MORI,Tatsuo YAMAUCHI and YASUHISA SAIKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     gomisin T
    ÏàËÆ¶È:76.9%
Tetrahedron Letters          2005          46          8467-8470
Regio- and stereoselective 12-O-demethylation of schizandrin into gomisin T, an important intermediate to gomisin A, by Mortierella sp. (TM-I1104)
Hirotoshi Kanatani, Susumu Terabayashi, Shuichi Takeda, Wei Li, Kazuo Koike, Tamotsu Nikaido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Neglschisandrin C
3Â¥2015-05-05 11:42:41
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1 .     beilschmin B
C24H32O7     ÏàËÆ¶È:65.3%
Planta Medica          2006          72          351-357
New Cytotoxic Tetrahydrofuran- and Dihydrofuran-Type Lignans from the Stem of Beilschmiedia tsangii
Jih-Jung Chen,En-Tzu Chou,Chang-Yih Duh,Sheng-Zehn Yang,Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (+)-yangabin
    ÏàËÆ¶È:65.3%
Phytochemistry          1993          32          1421-1424
Biotransformation of (+)-magnolin and (+)-yangabin in rat
Mitsuo Miyazawa, Hiroyuki Kasahara, Hiromu Kameoka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (+)-yangabin
    ÏàËÆ¶È:65.3%
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
4 .     Schinlignin A
C23H30O7     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          2010          58          1606-1611
Nortriterpenoids and Lignans from the Fruit of Schisandra chinensis
Yong-Bo XUE, Yan-Long ZHANG, Jian-Hong YANG, Xue DU, Jian-Xin PU, Wei ZHAO,Xiao-Nian LI, Wei-Lie XIAO, and Han-Dong SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     schinlignin A
C23H30O7     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          2010          58          1606-1611
Nortriterpenoids and Lignans from the Fruit of Schisandra chinensis
Yong-Bo Xue, Yan-Long Zhang, Jian-Hong Yang, Xue Du, Jian-Xin Pu, Wei Zhao, Xiao-Nian Li, Wei-Lie Xiao, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     bonaspectin A
C35H46O10     ÏàËÆ¶È:61.5%
Phytochemistry          2000          53          119-128
Bonaspectins and neobonaspectins,first sesquilignans and sesquineolignans from a convolvulaceous species
Britta Tofern, Kristina Jenett-Siems, Karsten Siems, Jasmin Jakupovic, Eckart Eich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     bonaspectin B
C35H46O10     ÏàËÆ¶È:61.5%
Phytochemistry          2000          53          119-128
Bonaspectins and neobonaspectins,first sesquilignans and sesquineolignans from a convolvulaceous species
Britta Tofern, Kristina Jenett-Siems, Karsten Siems, Jasmin Jakupovic, Eckart Eich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Ligraminol A
C23H30O6     ÏàËÆ¶È:61.5%
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   Ì¼Æ×Ä£Äâͼ
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