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jiangchunyong: ½ð±Ò+1, лл 2013-04-19 11:35:04
С̹½0018: ½ð±Ò+10, ¡ïÓаïÖú, ¶Ô²»ÉÏ£¬µ«ÊÇÓвο¼¼ÛÖµ£¬·Ç³£¸Ðл£¡ 2013-04-19 16:01:14
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jiangchunyong: ½ð±Ò+1, лл 2013-04-19 11:35:04
С̹½0018: ½ð±Ò+10, ¡ïÓаïÖú, ¶Ô²»ÉÏ£¬µ«ÊÇÓвο¼¼ÛÖµ£¬·Ç³£¸Ðл£¡ 2013-04-19 16:01:14
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1 . (E)-4-((1S,3R,4R)-1-hydroxy-4,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)but-1-en-3-o-ne C13H20O3 ÏàËÆ¶È:92.8% Journal of Asian Natural Products Research 2012 14 826-830 Two new compounds from Senecio cannabifolius Yi Tao, Wei Jiang, Yi-Yu Cheng & Yu-Feng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Á-hydroxy-5,6-epoxy-7-megastigmen-9-one ÏàËÆ¶È:92.8% Chinese Pharmaceutical Journal 2012 47 948-952 Chemical Constituents from Marine Alga Sargassum thunbergii JIANG Qian, LIU Dong, YANG Jia-bo, YAN Peng-cheng, HUANG Ke-xin, LIN Wen-han Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Annuionone D C13H20O3 ÏàËÆ¶È:85.7% 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 4 . (3S,5R,6S,7E)-5,6-epoxy-3-hydroxy-7-megastigmen-9-one C13H20O3 ÏàËÆ¶È:78.5% 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 5 . (3S,5R,6S,7E)-5,6-epoxy-3-hydroxy-7-megastigmene-9-one ÏàËÆ¶È:78.5% 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 6 . annuionone D C13H20O3 ÏàËÆ¶È:78.5% 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 7 . 3¦Á-hydroxy-5,6-epoxy-7-megastigmen-9-one C13H20O3 ÏàËÆ¶È:78.5% 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 8 . 3S,5R,6S,7E)-5,6-epoxy-3-hydroxy-7-megastigmen-9-one ÏàËÆ¶È:78.5% Journal of Shenyang Pharmaceutical University 2012 29 519-524 Isolation and identification of chemical constituents from the leaves of Nelumbo nucifera Gaertn. PENG Shuang; HAN Li-feng; LIU Er-wei; ZHANG Yi; WANG Tao Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastimen-9-one C13H20O3 ÏàËÆ¶È:71.4% 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 10 . compound 3 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 ̼Æ×Ä£Äâͼ 11 . (3S,5R,6S,7E)3,5,6-trihydroxy-7-megastigmen-9-one C13H22O4 ÏàËÆ¶È:71.4% Journal of Asian Natural Products Research 2007 9 321-325 Norisoprenoids from Ulva lactuca Y. SUN, Y.-C. ZHAN, Y. SHA and Y.-H. PEI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . annuionone D C13H20O3 ÏàËÆ¶È:71.4% 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 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastigmen-9-one ÏàËÆ¶È:71.4% Chinese Journal of Natural Medicines 2008 6 357-361 Chemical Constituents of Saussurea laniceps WANG Hong-Bing; CHU Wen-Jing; LI Gui-Rong; LAU Chu-Pak; QIN Guo-Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3¦Á-Hydroxy-5,6-epoxy-7-megastigmen-9-one ÏàËÆ¶È:71.4% 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 15 . 5,6-epoxy-3-hydroxy-7-megastigmen-9-ene C13H22O3 ÏàËÆ¶È:71.4% Natural Product Sciences 2009 15 246-249 Phytochemical Constituents of Thesium chinense TURCZ and Their Cytotoxic Activities In Vitro Lee, Il-Kyun; Kim, Ki-Hyun; Choi, Sang-Un; Lee, Jae-Hyun; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (E,1'R*,2'S*,3'S*,4'S*)-4-(1',2' :3'.4'-diepoxy-2',6',6'-trimethyl-1'-cyclohexyl)-3-buten-2-on C13H18O3 ÏàËÆ¶È:64.2% Helvetica Chimica Acta 1981 64 1766-1776 Photochemische Reaktionen 122. Mitteilung [1]. Zur vinylogen ¦Â-spaltung von epoxy-enonen: Photoisomerisierung des 3,4:5,6-diepoxy-5,6-dihydro-¦Â-jonons Norbert Bischofberger, Guy de Week, Bruno Frei, Hans Richard Wolf, Oskar Jerger Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-hydroxy-5,6-epoxy-¦Â-ionone ÏàËÆ¶È:64.2% Phytochemistry 1997 46 967-968 A quinoline alkaloid from Acanthosyris paulo-alvinii Juceni P. Ch¨¢vez, Ihanmarck D. dos Santos, Frederico G. Cruz, Jorge M. David, Shu-Wei Yang, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 5,6-Epoxy-3-hydroxy-7-megastigmen-9-one ÏàËÆ¶È:64.2% Archives of Pharmacal Research 2008 31 983-988 Terpene and phenolic constituents of Lactuca indica L. Ki Hyun Kim, Kyu Ha Lee, Sang Un Choi, Young Ho Kim and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . saussureoside A(1a) C13H20O4 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 2005 53(11) 1416-1422 Bioactive Constituents from Chinese Natural Medicines. XV.1) Inhibitory Effect on Aldose Reductase and Structures of Saussureosides A and B from Saussurea medusa Haihui XIE,Tao WANG,Hisashi MATSUDA,Toshio MORIKAWA,Masayuki YOSHIKAWA,and Tadato TANI Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (3S,5R,6S,7E,9R)-5,6-epoxy-3,9-dihydroxy-7-megastigmene C13H22O3 ÏàËÆ¶È:57.1% 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 21 . 3-hydroxy-5,6-epoxy-¦Â-ionone C13H20O3 ÏàËÆ¶È:57.1% Natural Product Research 1998 12 35-40 3-Hydroxy-5,6-Epoxy-¦Â-Ionone As Germination Inhibitory Active Constituent In Athyrium Yokoscense Masashi Kurokawa; Takayuki Hirose; Yuji Sugata; Munetaka Tokumasu; Yoshikazu Hiraga; Takayuki Suga Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 1,16-bis-(tetrahydro-pyran-2-yloxy)-hexadecan-8-ol ÏàËÆ¶È:57.1% Natural Product Research 2009 23 1029-1034 New synthesis of nematocidal natural products dithiocynates thiocyanatin A and 1,8,16-trihydroxyhexadecane Ashima Singh; M. L. Sharma; Jasvinder Singh Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . corchoionol A ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1997 45 464-469 Medicinal Foodstuffs. V. Moroheiya. (1) : Absolute Stereostructures of Corchoionosides A, B, and C, Histamine Release Inhibitors from the Leaves of Vietnamese Corchorus olitorius L. (Tiliaceae) Masayuki YOSHIKAWA,Hiromi SHIMADA,Masami SAKA,Satoshi YOSHIZUMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ |

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