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1 .     3-Hydroxy-5¦Á,6¦Á-epoxy-¦Â-ionone
C13H20O3     ÏàËÆ¶È:100%
Archives of Pharmacal Research          2004          27          600-603
Norisoprenoids and hepatoprotective flavone glycosides from the aerial parts of Beta vulgaris var. cicla
Inkyum Kim, Young-Won Chin, Song Won Lim, Young Choong Kim and Jinwoong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (3S,5R,6S,7E)-3,5,6-trihydroxy-7-megastigmen-9-one
    ÏàËÆ¶È:100%
Archives of Pharmacal Research          2011          34          533-542
Isolation of megastigmane sesquiterpenes from the silkworm (Bombyx mori L.) droppings and their promotion activity on HO-1 and SIRT1
Ji-Hae Park, Do-Gyeong Lee, Seung-Woo Yeon, Hyuk-Sang Kwon and Jong-Hee Ko, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastigmene
    ÏàËÆ¶È:92.3%
China Journal of Chinese Materia Medica          2006          31          1787-1790
Chemical constituents from red alga Corallina pilulifera
YUAN Zhaohui, HAN Lijun, FAN Xiao, LI Shuai, SHI Dayong, SUN Jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastigmen-9-one
    ÏàËÆ¶È:92.3%
China Journal of Chinese Materia Medica          2013          38          839-843
Chemical constituents from leaves of Rhododendron rubiginosum var. rubiginosum
YANG Yong-xun, YAN Yong-ming, TAO Ming, LUO Qian, DONG Xiao-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3¦Á-hydroxysulphonyloxy-5¦Á,6¦Á-epoxy-megastigmen-9-one
C13H20O6S     ÏàËÆ¶È:76.9%
Journal of Asian Natural Products Research          2008          10          319-321
A new sulphated nor-sesquiterpene from mangrove Laguncularia racemosa (L.) Gaertn. F.
Duo-Qing Xue, Ji-Dong Wang and Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-hydroxy-5¦Á,6¦Á-epoxy-¦Â-ionone
C13H20O3     ÏàËÆ¶È:76.9%
China Journal of Chinese Materia Medica          2007          32          120-123
Studies on chemical constituents of Laurencia tristicha
SUN Jie, HAN Lijun, SHI Dayong, FANG Xiao, YANG Yongchun , SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (3S,5R,6S,7E)-5,6-epoxy-3-hydroxy-7-rnegastigmen-9-one
C13H20O3     ÏàËÆ¶È:76.9%
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
8 .     (3S,5R,6S,7E)-5,6-epoxy-3-hydroxy-7-megastigmen-9-one
C13H20O3     ÏàËÆ¶È:69.2%
Phytochemistry          2004          65          497-505
Structure elucidation and phytotoxicity of C13 nor-isoprenoids from Cestrum parqui
Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Palma Oriano, Fabio Temussi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (3S,5R,6R,7E,9R) - 3,5,6,9 - tetrahydroxy - 7 - megastigmene
C13H24O4     ÏàËÆ¶È:69.2%
Phytochemistry          2004          65          497-505
Structure elucidation and phytotoxicity of C13 nor-isoprenoids from Cestrum parqui
Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Palma Oriano, Fabio Temussi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastimen-9-one
C13H20O3     ÏàËÆ¶È:69.2%
Phytochemistry          2002          59          85-90
Immunosuppressive constituents from Saussurea medusa
Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto,Takao Taki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 3
    ÏàËÆ¶È:69.2%
Journal of Asian Natural Products Research          2008          10          319-321
A new sulphated nor-sesquiterpene from mangrove Laguncularia racemosa (L.) Gaertn. F.
Duo-Qing Xue, Ji-Dong Wang and Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     annuionone D
C13H20O3     ÏàËÆ¶È:69.2%
Phytochemistry          1999          52          613-621
Allelochemicals from sunflower leaves cv. Peredovick
Francisco A. Mac¨ªas, Rosa M. Oliva, Rosa M. Varel, Ascensi¨®n Torres, Jos¨¦ M.G. Molinillo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (3S,5R,6S,7E)-5,6-epoxy-3-hydroxy-7-megastigmene-9-one
    ÏàËÆ¶È:69.2%
Canadian Journal of Chemistry          2008          86          892-898
Chemical-constituent diversity of Tridax procumbens
Wen-Hao Chen, Xing-Ming Ma, Quan-Xiang Wu, and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     annuionone D
C13H20O3     ÏàËÆ¶È:69.2%
Chinese Traditional and Herbal Drugs          2008          39          1466-1468
äýéÂľ½ª×ÓÖлÆÍªÀà³É·ÖÑо¿
ÍôÔÆËÉ;»ÆÈÙ;ÀîÁ¼;Õźé±ò;Ñ»ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3¦Á-hydroxy-5,6-epoxy-7-megastigmen-9-one
C13H20O3     ÏàËÆ¶È:69.2%
Chinese Traditional and Herbal Drugs          2001          32          390-391
Studies on chemical constituents of Toona sinensis
LUO Xiao dong; WU Shao hua; MA Yun bao; Wu Da gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     3¦Á-Hydroxy-5,6-epoxy-7-megastigmen-9-one
    ÏàËÆ¶È:69.2%
Archives of Pharmacal Research          2007          30          1067-1074
Lignan and terpene constituents from the aerial parts of saussurea pulchella
Sang Un Choi, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Annuionone D
C13H20O3     ÏàËÆ¶È:69.2%
Journal of China Pharmaceutical University          2010          41          26-28
Chemical constituents from Senecio nemorensis
SHI Bao-jun; CHOU Gui-xin; WANG Zheng-tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-12-11 16:57:47
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