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tbdlh0413ͳæ (ÕýʽдÊÖ)
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[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (126 MHz, CDCL3) ¦Ä 14.13,19.65,19.75, 22.64, 22.70, 22.73, 24.46,24.80,27.99,29.38,29.67,29.71,31.94,32.79,37.29,37.41,39.38,55.90,56.47,92.83,97.58,103.97,115.68,116.81,117.48,120.37,121.56,121.73,123.63,124.72,125.68,128.86,130.92,131.34,146.31,148.28,149.58,157.60,159.07,163.36,166.78,180.82 |
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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
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tbdlh0413: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2014-04-05 20:33:28
À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-06 08:50:07
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tbdlh0413: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2014-04-05 20:33:28
À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-06 08:50:07
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²éѯ½á¹û£º¹²²éµ½51¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Lumutinine A C42H48N4O4 ÏàËÆ¶È:57.1% Journal of Natural Products 2011 74 2556-2562 Lumutinines A¨CD, Linearly Fused Macroline¨CMacroline and Macroline¨CSarpagine Bisindoles from Alstonia macrophylla Siew-Huah Lim, Shin-Jowl Tan, Yun-Yee Low, and Toh-Seok Kam Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound A-05 C42H55NO4 ÏàËÆ¶È:54.7% Molecules 2013 18 3615-3629 Efficient Synthesis and Anti-Fungal Activity of Oleanolic Acid Oxime Esters Hanqing Zhao, Minjie Zhou, Lifeng Duan, Wei Wang, Jianjun Zhang, Daoquan Wang and Xiaomei Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 4 C39H54O5 ÏàËÆ¶È:52.3% Phytochemistry 1999 51 683-687 Triterpene caffeoyl esters and diterpenes from Celastrus stephanotifolius Bei Chen, Hongquan Duan, Yoshihisa Takaishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 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Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . olean-28-al-3¦Â-yl-caffeate ÏàËÆ¶È:52.3% China Journal of Chinese Materia Medica 2010 35 323-326 Immunosuppressive triterpenes from Tetraena mongolica DING Linlin; LIU Qiang; HU Jiaxu; TANG Sheng an; DUAN Hongquan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Á-[(E)-Feruloyloxy]-D:C-friedooleana-7,9(11)-dien-29-oic Acid C40H54O6 ÏàËÆ¶È:52.3% Helvetica Chimica Acta 2010 93 1355-1361 Triterpenoids from the Stems of Momordica charantia Chiy-Rong Chen, Yun-Wen Liao, Wen-Ling Shih, Chih-Ying Tzeng, Hsueh-Ling Cheng, Wei-Tsung Kao and Chi-I Chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Á-O-trans-Feruloylbetulinic acid C40H56O6 ÏàËÆ¶È:52.3% Journal of Asian Natural products Research 2010 12 576-581 Three new lupane-type triterpenes from Ceriops tagal Xia-Chang Wang; Xiao-Wei Ouyang; Li-Hong Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 5-isopropoxy-2-(8-isopropoxy-1-(4-isopropoxy-3-methoxyphenyl)-9-methoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-2-yl)-4-methoxyphenyl methanesulfonate C37H45NO9S ÏàËÆ¶È:52.3% European Journal of Medicinal Chemistry 2010 45 11-18 Novel hybrids from lamellarin D and combretastatin A 4 as cytotoxic agents Li Shen, Xiaochun Yang, Bo Yang, Qiaojun He, Yongzhou Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â,21¦Â,24-trihydroxyserrat-14-en-24-(4'-hydroxybenzoate) C37H54O5 ÏàËÆ¶È:52.3% Planta medica 2012 78 1387-1391 New Serratene Triterpenoids from Palhinhaea cernua and Their Cytotoxic Activity Yan, Jian; Zhou, Zhong-Yu; Zhang, Mei; Wang, Jing; Dai, Hao-Fu; Tan, Jian-Wen: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound A-07 C37H50FNO4 ÏàËÆ¶È:52.3% Molecules 2013 18 3615-3629 Efficient Synthesis and Anti-Fungal Activity of Oleanolic Acid Oxime Esters Hanqing Zhao, Minjie Zhou, Lifeng Duan, Wei Wang, Jianjun Zhang, Daoquan Wang and Xiaomei Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . N,N-dimethyl-(3¦Â-acetate-ergosta-5,7,12-triene)-N-octylammonium bromide C40H68NO2Br2 ÏàËÆ¶È:52.3% Molecules 2013 18 14961-14976 Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols Bogumił Brycki, Hanna Koenig, Iwona Kowalczyk and Tomasz Pospieszny Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . N,N-dimethyl-(3¦Â-acetate-ergosta-5,7,12-triene)-N-decylammonium bromide C42H71NO2Br2 ÏàËÆ¶È:52.3% Molecules 2013 18 14961-14976 Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols Bogumił Brycki, Hanna Koenig, Iwona Kowalczyk and Tomasz Pospieszny Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . siphonein ÏàËÆ¶È:52.1% Phytochemistry 1984 23 649-655 Algal carotenoids with novel end groups Anne Fiksdahl, Terje Bjørnland, Synnøve Liaaen-Jensen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (¡À)-3-chloro-6,7,10,11-tetrahydro-N-2-4-6-3,4-dihydro-6,7-dimethoxy-1-3-nitrophenylisoquinolin-21H-ylhexyl-1H-1,2,3-triazol-1-yl-9-methyl-12-amino-6,10-methanocyclooctaquinoline ÏàËÆ¶È:51.1% Bioorganic & Medicinal Chemistry 2009 17 4523-4536 Synthesis and structure¨Cactivity relationship of Huprine derivatives as human acetylcholinesterase inhibitors Cyril Ronco, Geoffroy Sorin, Florian Nachon, Richard Foucault, Ludovic Jean, Anthony Romieu, Pierre-Yves Renard Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . streptocidin D ÏàËÆ¶È:51.1% The Journal of Antibiotics 2001 54 434-440 Streptocidins A-D, Novel Cyclic Decapeptide Antibiotics Produced by Streptomyces sp. T¨¹ 6071 II. Structure Elucidation ALEXANDRA HÖLTZEL,RALPH W. JACK,GRAEME J. NICHOLSON,G¨¹NTHER JUNG,KLAUS GEBHARDT,HANS-PETER FIEDLER and RODERICH D. S¨¹SSMUTH Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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