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793487509: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, лл°ïÖú 2013-12-12 11:36:50
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793487509: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, лл°ïÖú 2013-12-12 11:36:50
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²éѯ½á¹û£º¹²²éµ½177¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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