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huzuyanгæ (³õÈëÎÄ̳)
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[ÇóÖú]
΢Æ×½á¹¹ÇóÖú-9
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| 13C NMR (101 MHz, MeOD) ¦Ä11.84, 12.03, 12.19, 15.58, 18.46, 19.01, 19.22, 19.37, 20.02, 20.42, 20.90, 21.27, 23.24, 24.51, 26.06, 26.59, 28.49, 28.76, 29.29, 29.46, 29.58, 29.67, 29.92, 31.56, 31.76, 32.63, 34.09, 36.05, 36.31, 36.64, 37.13, 37.20, 37.60, 37.70, 39.02, 39.36, 39.75, 41.10, 41.92, 42.20, 42.34, 42.45, 43.13, 46.01, 48.44, 49.62, 55.55, 55.89, 56.15, 65.57, 71.54, 71.64, 73.56, 124.06, 125.64,143.68, 146.46¡£ |
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huzuyan: ½ð±Ò+10, ¡ïÓаïÖú, лл°ïæ 2013-07-08 14:34:23
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huzuyan: ½ð±Ò+10, ¡ïÓаïÖú, лл°ïæ 2013-07-08 14:34:23
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1 . amaroxocane A C55H85Na3O17S3 ÏàËÆ¶È:64.9% Journal of Natural Products 2009 72 259-264 Amaroxocanes A and B: Sulfated Dimeric Sterols Defend the Caribbean Coral Reef Sponge Phorbas amaranthus from Fish Predators Brandon I. Morinaka, Joseph R. Pawlik, and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . fibrosterol sulfate A C54H84O19S4Na4 ÏàËÆ¶È:61.4% The Journal of Organic Chemistry 2009 74 5902-5908 Fibrosterol Sulfates from the Philippine Sponge Lissodendoryx (Acanthodoryx) fibrosa: Sterol Dimers that Inhibit PKC¦Æ Emily L. Whitson, Tim S. Bugni, Priya S. Chockalingam, Gisela P. Concepcion, Xidong Feng, Guixian Jin, Mary Kay Harper, Gina C. Mangalindan, Leonard A. McDonald and Chris M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . hamigerol B C56H85Na5O23S5 ÏàËÆ¶È:57.8% Journal of Natural Products 2007 70 1195-1199 Hamigerols A and B, Unprecedented Polysulfate Sterol Dimers from the Mediterranean Sponge Hamigera hamigera Jie-Fei Cheng, Jong-Soo Lee, Furong Sun, Elizabeth A. Jares-Erijman, Sue Cross, and Kenneth L. Rinehart Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . fibrosterol Sulfate B C54H83O22S5Na5 ÏàËÆ¶È:57.8% The Journal of Organic Chemistry 2009 74 5902-5908 Fibrosterol Sulfates from the Philippine Sponge Lissodendoryx (Acanthodoryx) fibrosa: Sterol Dimers that Inhibit PKC¦Æ Emily L. Whitson, Tim S. Bugni, Priya S. Chockalingam, Gisela P. Concepcion, Xidong Feng, Guixian Jin, Mary Kay Harper, Gina C. Mangalindan, Leonard A. McDonald and Chris M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . fibrosterol Sulfate C C54H84O19S4Na4 ÏàËÆ¶È:57.8% The Journal of Organic Chemistry 2009 74 5902-5908 Fibrosterol Sulfates from the Philippine Sponge Lissodendoryx (Acanthodoryx) fibrosa: Sterol Dimers that Inhibit PKC¦Æ Emily L. Whitson, Tim S. Bugni, Priya S. Chockalingam, Gisela P. Concepcion, Xidong Feng, Guixian Jin, Mary Kay Harper, Gina C. Mangalindan, Leonard A. McDonald and Chris M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . crellastatin I C58H88O11S ÏàËÆ¶È:56.8% Tetrahedron 1999 55 13749-13756 Isolation and structural elucidation of the crellastatins I-M: cytotoxic bis-steroid derivatives from the vanuatu marine sponge Crella sp Clelia Giannini, Angela Zampella, Cecile Debitus, Jean-Louis Menou, Christos Roussakis, Maria Valeria D'Auria Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . amaroxocane B C54H82Na3O20S4 ÏàËÆ¶È:56.1% Journal of Natural Products 2009 72 259-264 Amaroxocanes A and B: Sulfated Dimeric Sterols Defend the Caribbean Coral Reef Sponge Phorbas amaranthus from Fish Predators Brandon I. Morinaka, Joseph R. Pawlik, and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . hamigerol A C56H84Na4O20S4 ÏàËÆ¶È:56.1% Journal of Natural Products 2007 70 1195-1199 Hamigerols A and B, Unprecedented Polysulfate Sterol Dimers from the Mediterranean Sponge Hamigera hamigera Jie-Fei Cheng, Jong-Soo Lee, Furong Sun, Elizabeth A. Jares-Erijman, Sue Cross, and Kenneth L. Rinehart Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . shishicrellastatin A C56H83Na3O16S3 ÏàËÆ¶È:54.3% Bioorganic & Medicinal Chemistry 2011 19 6594-6598 Shishicrellastatins, inhibitors of cathepsin B, from the marine sponge Crella (Yvesia) spinulata Shuhei Murayama, Yasufumi Imae, Kentaro Takada, Jo Kikuchi, Yoichi Nakao, Rob W.M. van Soest, Shigeru Okada, Shigeki Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . shishicrellastatin B C56H81Na3O16S3 ÏàËÆ¶È:54.3% Bioorganic & Medicinal Chemistry 2011 19 6594-6598 Shishicrellastatins, inhibitors of cathepsin B, from the marine sponge Crella (Yvesia) spinulata Shuhei Murayama, Yasufumi Imae, Kentaro Takada, Jo Kikuchi, Yoichi Nakao, Rob W.M. van Soest, Shigeru Okada, Shigeki Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 23-(6-Methyl)heptanoic acid demalonylazalomycin F3a ester C60H105N3O15 ÏàËÆ¶È:51.6% Marine Drugs 2013 11 817-829 New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells Ganjun Yuan, Kui Hong, Haipeng Lin, Zhigang She and Jia Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . H-¦Â3hVal-¦Â3hLys-¦Â3hSer(X)-¦Â3hPhe-¦Â3hGlu-¦Â3hSer(X)-¦Â3hTyr-¦Â3hIle-OH C58H91N9O14 ÏàËÆ¶È:50.8% Helvetica Chimica Acta 2009 92 2643-2658 Synthesis and High-Resolution NMR Structure of a ¦Â3-Octapeptide with and without a Tether Introduced by Olefin Metathesis Marc-Olivier Ebert, James Gardiner, Steven Ballet, Andrew D. Abell, Dieter Seebach Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . auriculatusaponin F Cl57H90O25 ÏàËÆ¶È:50.8% Journal of Asian Natural Products Research 1998 1 1-14 Triterpenoid Saponins from Aster auriculatus CHANG ZENG WANG and DE QUAN YU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3-O-¦Â-D-ßÁà«Ä¾ÌÇ»ù-(1¡ú2)-¦Â-D-ßÁà«ÆÏÌÑÌÇÈ©Ëá»ù-3¦Â,21¦Â,22¦Â,23,29-ÎåôÇ»ùÆë¶Õ¹û-12-Ï©-21-O-¦Á-(2,3,4-O-ÈýÒÒõ£»ù)-L-ÊóÀîÌÇß° C53H82O22 ÏàËÆ¶È:50.8% Journal of Tropical and Subtropical Botany 1998 6 357-361 ÂíÀ´²æÖù»¨Ò¶ÖеÄÒ»¸öÐÂÌðζ߰µÄ½á¹¹ ÅËÎĶ·, ƱÔÁ¼Ö¦, ³àÓðÕÉÃ÷, ´ó¹ÈÔ£Ö®, ÈÕ¹üÑÇÎ÷ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 3-O-¦Á-L-rhamnopyranosyl-(1¡ú4)-¦Â-D-galactopyranosyl-(1¡ú3)[¦Â-D-glucopyranosyl-(1¡ú2)]-¦Â-D-glucuronopyranosyl 22-O-angeloylerythrodiol C59H94O24 ÏàËÆ¶È:50.8% Journal of Natural Products 2008 71(5) 918-921 Acylated Triterpenoid Saponins from Schima noronhae and Their Cell Growth Inhibitory Activity Takashi Ohtsuki, Takashi Miyagawa, Takashi Koyano, Thaworn Kowithayakorn, Nobuo Kawahara, Yukihiro Goda, and Masami Ishibashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 23-Valine demalonylazalomycin F5a ester C59H104N4O15 ÏàËÆ¶È:50.8% Marine Drugs 2013 11 817-829 New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells Ganjun Yuan, Kui Hong, Haipeng Lin, Zhigang She and Jia Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . dipteroside B C58H90O22 ÏàËÆ¶È:50% Helvetica Chimica Acta 2008 Vol. 91 1728 Triterpenoid Ester Saponins from Dipteronia dyeriana Rong Guo, Min Luo, Chun-Lin Long, Ma-Lin Li, Zhi-Qin Ouyang, Yi-Ping Zhou, Yue-Hu Wang, Xing-Yu Li, and Ya-Na Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . dipteroside D C60H92O22 ÏàËÆ¶È:50% Helvetica Chimica Acta 2008 Vol. 91 1728 Triterpenoid Ester Saponins from Dipteronia dyeriana Rong Guo, Min Luo, Chun-Lin Long, Ma-Lin Li, Zhi-Qin Ouyang, Yi-Ping Zhou, Yue-Hu Wang, Xing-Yu Li, and Ya-Na Shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . malonyl-4,5-dihydroniphimycin C62H107N3O21 ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2007 62b 1187-1192 Malonyl-4, 5-dihydroniphimycin: A New Polyol Macrolide Antibiotic, Produced by Streptomyces hygroscopicus Veneta Ivanova, Mariana Kolarova, and Krasja Aleksieva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . crellastatin J C58H88O13S ÏàËÆ¶È:50% Tetrahedron 1999 55 13749-13756 Isolation and structural elucidation of the crellastatins I-M: cytotoxic bis-steroid derivatives from the vanuatu marine sponge Crella sp Clelia Giannini, Angela Zampella, Cecile Debitus, Jean-Louis Menou, Christos Roussakis, Maria Valeria D'Auria Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . crellastatin M C58H88O15S2 ÏàËÆ¶È:50% Tetrahedron 1999 55 13749-13756 Isolation and structural elucidation of the crellastatins I-M: cytotoxic bis-steroid derivatives from the vanuatu marine sponge Crella sp Clelia Giannini, Angela Zampella, Cecile Debitus, Jean-Louis Menou, Christos Roussakis, Maria Valeria D'Auria Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 3-O-{¦Â-D-xylopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl-(1¡ú6)-2-acetamido-2-deoxy-¦Â-D-glucopyranosyl}echinocystic acid 28-O-{¦Â-D-apiofuranosyl-(1¡ú2)-¦Â-D-xylopyranosyl} ester C58H93NO25 ÏàËÆ¶È:50% Natural Product Communications 2008 3 1763-1770 Triterpenoidal Saponins and Prosapogenins fromAlbizia lebbeck (Leguminosae) Janelle P. Scott, Winston F. Tinto and William F. Reynolds Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- Copyright © 2009-2011 ÉϺ£Î¢Æ×ÐÅÏ¢¼¼ÊõÓÐÏÞ¹«Ë¾ Shanghai Micronmr Infor Technology Co., Ltd., All Rights Reserved |
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