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1 .     rel-(7R,8R,7'R,8'R)-3 ,4-Methylenedioxy-3,4,5,5'-tetramethoxy-7,7'-epoxylignan
     ÏàËÆ¶È:81.8%
Chemistry of Natural Compounds          2010          46          450-451
Lignans from Saururus chinensis
Lishu Wang, Xuefeng Zhou, Tunhai Xu, Xianwen Yang and Yonghong Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     seartemin
     ÏàËÆ¶È:66.6%
Fitoterapia          1999          70          89-92
Antibacterial furofuran lignans from Canary Islands propolis
R. Christov, V. Bankova, I. Tsvetkova, A. Kujumgiev,A. Delgado Tejera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     rel-(7S,8S,7 'R,8 'R)-3,3 ',4,4 ',5,5 '-hexamethoxy-7.O.7 ',8.8 '-lignan
C24H32O7     ÏàËÆ¶È:66.6%
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

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4 .     (7S,8S,7'S,8'S)-3,4,5-trimethoxy3',4'-methylenedioxy-7,7'-epoxylignan
     ÏàËÆ¶È:66.6%
Phytochemistry          1996          43          1089-1092
Lignans, ¦Ã-lactones and propiophenones of Virola surinamensis
Norberto Peporine Lopes, Ema Ester de Almeida Blumenthal, Alberto Jos¨¦ Cavalheiro, Massuo Jorge Kato, Massayoshi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     rel-(7R,8R,7'R,8'R)-3',4'-methylenedioxy-3,4,5,5'-tetramethoxy-7,7'-epoxylignan
C23H28O7     ÏàËÆ¶È:65.2%
Phytochemistry          2003          64          667-670
Trypanocidal tetrahydrofuran lignans from inflorescences of Piper solmsianum
Roberto C.C. Martins, João Henrique G. Lago, Sergio Albuquerque,Massuo J. Kato
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     episesartemin B
     ÏàËÆ¶È:65%
Phytochemistry          2002          59          851-856
Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea
Ahmed A. Ahmed, Ahmed A. Mahmoud, Eptehal T. Ali, Olga Tzakou,Maria Couladis, Tom J. Mabry, Tam¨¢s G¨¢tid, G¨¢bor T¨®th
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     beilschminol A
C22H26O7     ÏàËÆ¶È:63.6%
Journal of Natural Products          2011          74          1875-1880
Anti-inflammatory Endiandric Acid Analogues from the Roots of Beilschmiedia tsangii
Yun-Ting Huang, Hsun-Shuo Chang, Guei-Jane Wang, Ming-Jen Cheng, O Chu-Huang Chen, Yi-Jen Yang, and Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     sesartemin
     ÏàËÆ¶È:63.1%
Phytochemistry          2002          59          851-856
Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea
Ahmed A. Ahmed, Ahmed A. Mahmoud, Eptehal T. Ali, Olga Tzakou,Maria Couladis, Tom J. Mabry, Tam¨¢s G¨¢tid, G¨¢bor T¨®th
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Sesartemin
     ÏàËÆ¶È:63.1%
Journal of Chinese Pharmaceutical Sciences          2012          21          360-364
Nine lignans from Artemisia absinthium L.
Abulajiang¡¤Tulake; Yong Jiang; Peng-Fei Tu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     2-Episesalatin
     ÏàËÆ¶È:60%
Phytochemistry          1992          31          2911-2912
A furofuran lignan from Sesamum alatum
Afaf Kamal-Eldin, Gariballa Yousif
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     7'-epi-sesartemin
     ÏàËÆ¶È:60%
Pharmaceutical Biology          2005          43          378-381
A New Larvicidal Lignan from Piper fimbriulatum.
Pablo N. Sol¨ªs, Dionisio Olmedo, Norio Nakamura, Ángela I. Calder¨®n, Masao Hattori, Mahabir P. Gupta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     beilschminol B
C23H30O7     ÏàËÆ¶È:60%
International Journal of Molecular Sciences          2012          13          16430-16443
Secondary Metabolites from the Roots of Beilschmiedia tsangii and Their Anti-Inflammatory Activities
Yun-Ting Huang, Hsun-Shuo Chang, Guei-Jane Wang, Chu-Hung Lin and Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     epi-sesartemin
C23H28O8     ÏàËÆ¶È:59.0%
Phytochemistry          1985          24          561-566
Non-alkaloidal constituents of Virola elongata bark
W. Donald MacRae, G. H. Neil Towers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     (7S,8S,7'S,8'S)-3,4,5,3',4'-pentarnethoxy-7,7'-epoxylignan
     ÏàËÆ¶È:57.8%
Phytochemistry          1996          43          1089-1092
Lignans, ¦Ã-lactones and propiophenones of Virola surinamensis
Norberto Peporine Lopes, Ema Ester de Almeida Blumenthal, Alberto Jos¨¦ Cavalheiro, Massuo Jorge Kato, Massayoshi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     futokadsurin C
C21H24O5     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2005          53(1)          121-124
Neolignans from Piper futokadsura and Their Inhibition of Nitric Oxide Production
Tenji KONISHI,Takao KONOSHIMA,Akihiro DAIKONYA,and Susumu KITANAKAc
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (2R,3S,3aS)-3a-allyl-5-methoxy-2-(3-methoxy-4,5-methylenedioxyphenyl)-3-methyl-2,3,3a,6-tetrahydro-6-oxobenzofuan
C21H22O6     ÏàËÆ¶È:57.1%
Journal of Natural Products          1991          Vol 54          1153
Bioactive Neolignans from Endlicheria dysodantha
Wen Wen Ma, John F. Kozlowski, Jerry L. McLaughlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     fragransin D1
C22H28O6     ÏàËÆ¶È:57.1%
Phytochemistry          1988          27          563-568
New neolignans and lignans from the aril of Myristica fragrans
Sumitra Hada,Masao Hattori,Yasuhiro Tezuka,Tohru Kikuchi,Tsuneo Namba
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     machilin-G
     ÏàËÆ¶È:57.1%
Phytochemistry          1988          27          634-636
Lignans from Machilus thunbergii
Hiroko Shimomura,Yutaka Sashida,Motomu Oohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     rel-(7R,8S,7'S,8'S)-9-hydroxy-4',5'-methylenedioxy-3,4,5,3'-tetramethoxy-7,7'-epoxylignan
C23H28O8     ÏàËÆ¶È:56.5%
Phytochemistry          2008          69          445-450
Trypanocidal tetrahydrofuran lignans from Peperomia blanda
Lidiane Gaspareto Felippe, Debora Cristina Baldoqui, Massuo Jorge Kato,Vanderlan da Silva Bolzani, Elsie Franklin Guimarães, Regina Maria Barreto Cicarelli,Maysa Furlan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     4¦Á,5¦Á-epoxybeilschmin A
C23H26O8     ÏàËÆ¶È:56.5%
Planta Medica          2007          73          567-571
Novel Epoxyfuranoid Lignans and Antitubercular Constituents from the Leaves of Beilschmiedia tsangii
Jih-Jung Chen ,En-Tzu Chou, Chien-Fang Peng ,Ih-Sheng Chen ,Sheng-Zehn Yang,Hung-Yi Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-27 16:11:08
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