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mengzhu027: ½ð±Ò+8 2015-03-03 14:18:28
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mengzhu027: ½ð±Ò+8 2015-03-03 14:18:28
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1 . 3-Hydroxy-5¦Á,6¦Á-epoxy-¦Â-ionone C13H20O3 ÏàËÆ¶È:92.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (3S,5R,6S,7E)-3,5,6-trihydroxy-7-megastigmen-9-one C13H19O4 ÏàËÆ¶È:92.8% Natural Product Research and Development 2013 25 1658-1661 Chemical Constituents from Croton caudatus var. tomentosus ZHONG Jin-dong, LI Yan-ping, LI Hong-mei, LI Hai-zhou, LI Rong-tao* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (3S,5R,6S,7E)-3,5,6-trihydroxy-7-megastigmen-9-one ÏàËÆ¶È:92.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3S,5R,6S,7E)-3,5,6-trihydroxy-7-megastigmen-9-one C13H22O4 ÏàËÆ¶È:92.8% Chinese Journal of New Drugs 2013 22 713-718 Sesquiterpenes and cyclopeptides from the aerial parts of Jatropha curcas Linn. XU Jun-ju, TAN Ning-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-hydroxy-5,6-epoxy-7-megastigmen-9-one C13H20O3 ÏàËÆ¶È:92.8% Chinese Traditional and Herbal Drugs 2014 45 1228-1231 Chemical constituents from stems and leaves of Humulus scandens XU Bo, JIN Ying-jin, WANG Yi-han, SUN Juan, LI Xi-feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-hydroxy-5,6-epoxy-7-megastigmen-9-one ÏàËÆ¶È:92.8% Chinese Traditional and Herbal Drugs 2014 45 1228-1231 Chemical constituents from stems and leaves of Humulus scandens XU Bo, JIN Ying-jin, WANG Yi-han, SUN Juan, LI Xi-feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastigmene ÏàËÆ¶È:85.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastigmen-9-one ÏàËÆ¶È:85.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-¦Â-ionone C13H20O3 ÏàËÆ¶È:78.5% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (3S,5R,6S,7E)-5,6-epoxy-3-hydroxy-7-rnegastigmen-9-one C13H20O3 ÏàËÆ¶È:78.5% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastigmen-9-one ÏàËÆ¶È:78.5% Marine Sciences 2012 36 81-84 Monoterpene constituents of the brown alga Dictyopteris divaricata Okam. XU Xiu-li, YIN Li-yuan, SONG Fu-hang, FAN Xiao, SHI Jian-gong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Á-hydroxysulphonyloxy-5¦Á,6¦Á-epoxy-megastigmen-9-one C13H20O6S ÏàËÆ¶È:71.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 9¦Â-hydroxy-8-oxo-12-noreremophil-6-en-11-one C14H20O3 ÏàËÆ¶È:64.2% Helvetica Chimica Acta 2008 Vol. 91 1045 Eremophilane-Type Sesquiterpenes from the Roots of Ligularia virgaurea Zhan-Xin Zhang, Dong-Qing Fei, and Zhong-Jian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (3S,5R,6R,7E,9R) - 3,5,6,9 - tetrahydroxy - 7 - megastigmene C13H24O4 ÏàËÆ¶È:64.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastimen-9-one C13H20O3 ÏàËÆ¶È:64.2% Phytochemistry 2002 59 85-90 Immunosuppressive constituents from Saussurea medusa Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto,Takao Taki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 9-bromo-3,3,7-trimethyltricyclo[5.4.0.02,9]undecan-8-one C14H21OBr ÏàËÆ¶È:64.2% Journal of Natural Products 2003 66 520-523 An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene Sasan Karimi, and Paula Tavares Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 3 ÏàËÆ¶È:64.2% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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