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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
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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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·, ƱԭÁ¼Ö¦, ³àÓðÕÉÃ÷, ´ó¹ÈÔ£Ö®, ÈÕ¹üÑÇÎ÷
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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