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jun_crystalͳæ (³õÈëÎÄ̳)
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13C NMR (600 MHz,pyridine-d5) ¦Ä 14.76,23.41,26.37,29.99,30.08,30.10,30.31,30.35,30.41,30.49,32.58,32.60,33.23,33.36,33.44,36.14,55.04,63.09,70.68,71.94,72.74,72.95,75.60,78.93,79.07,106.20,130.39,131.57,132.50,132.55,176.10. |
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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jun_crystal: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-07-20 14:08:06
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jun_crystal: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-07-20 14:08:06
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°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½268¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . soya-cerebroside I C40H75NO9 ÏàËÆ¶È:90.3% Natural Product Sciences 2001 7 27-32 Isolation of Soya-cerebroside I from the Roots of Trichosanthes kirilowii Kim, Ju-Sun; Byun, Ji-Hye; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . phalluside 4 C42H77NO9 ÏàËÆ¶È:90.3% Tetrahedron 1998 54 14597-14602 Phallusides, new glucosphingolipids from the ascidian Phallusia fumigata Rosario Dur¨¢n, Eva Zub¨ªa, Mar¨ªa J. Ortega, Santiago Naranjo, Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . cerebroside C48H91NO9 ÏàËÆ¶È:87.5% Phytochemistry 1998 49 2403-2408 Glycosides from Stenochlaena palustris Hongmei Liu, Jimmy Orjala, Topul Rali, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . soyacerebroside II ÏàËÆ¶È:87.0% Chinese Pharmaceutical Journal 2008 43 971-973 Studies on Chemical Constituents of Acetyl Acetate Extracted Fraction from Veratrum dahuricum NIE Li-yue TANG Jian~LI Hui-liang JIN Hui-zi ZHANG Wei-dong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . lucyobroside C39H73O9N ÏàËÆ¶È:87.0% Natural Product Research and Development 1996 8(3) 20-25 A NEW CEREBROSIDE FROM LUFFA CYLINDRICA (L)ROEM Fang Zhapu; Zeng Xianyi; Xiong Shuling Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1,3,5-trihydroxy-2-hexadecanoylamino-9-(E)-heptacosene ¦Â-D-glucopyranoside derivative C48H93NO9 ÏàËÆ¶È:81.2% Phytochemistry 2002 61 1005-1008 Sphingolipids from Conyza canadensis Naveen Mukhtar, Kiran Iqbal, Itrat Anis, Abdul Malik Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . cerebroside ÏàËÆ¶È:81.2% Indian Journal of Chemistry 2007 46B 1868-1872 Antifungal and phytochemical studies of Eupatorium birmanicum DC. Devi,L Reena; Singh,Th Shyamkeshor; Laitonjam,Warjeet S Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . agelasphin-10 C49H90NO9 ÏàËÆ¶È:81.2% Tetrahedron 1994 50 2771-2784 Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus Takenori Natori, Masahiro Morita, Kohji Akimoto, Yasuhiko Koezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . agelasphin-12 C50H93NO9 ÏàËÆ¶È:81.2% Tetrahedron 1994 50 2771-2784 Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus Takenori Natori, Masahiro Morita, Kohji Akimoto, Yasuhiko Koezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . aralia cerebroside (1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydorxypalmitoylamino]-8-octadecene-1,3,4-triol) ÏàËÆ¶È:80.6% Korean Journal of Pharmacognosy 2006 37(2) 81-84 Isolation of a Cerebroside from Panax notoginseng Cho, Min-Jung; Lee, So-Young; Kim, Ju-Sun; Lee, Je-Hyun; Choi, Hwan-Soo; Lee, Ho-Young; Ha, Hye-Kyung; Kim, Chung-Sook; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . phalluside 1 C41H75NO9 ÏàËÆ¶È:80.6% Tetrahedron 1998 54 14597-14602 Phallusides, new glucosphingolipids from the ascidian Phallusia fumigata Rosario Dur¨¢n, Eva Zub¨ªa, Mar¨ªa J. Ortega, Santiago Naranjo, Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . phalluside 3 C42H77NO9 ÏàËÆ¶È:80.6% Tetrahedron 1998 54 14597-14602 Phallusides, new glucosphingolipids from the ascidian Phallusia fumigata Rosario Dur¨¢n, Eva Zub¨ªa, Mar¨ªa J. Ortega, Santiago Naranjo, Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . aralia cerebroside C40H77NO10 ÏàËÆ¶È:77.4% Journal of Natural Products 1999 62 1059-1060 Isolation of a New Cerebroside from the Root Bark of Aralia elata Sam Sik Kang, Ju Sun Kim, Yong Nan Xu, and Young Hee Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,9E)-2-(2'R-hydroxyhexadecenoy)-4,9-octadecadiene-1,3-diol C40H75O9N ÏàËÆ¶È:77.4% Natural Product Research 2006 20 1187-1191 A new cerebroside from fruits of Ailanthus altissima Swingle Chun-Chao Zhao; Jian-Hua Shao; Nan Wang; Xian Li; Jin-Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . aralia cerebroside ÏàËÆ¶È:77.4% Archives of Pharmacal Research 2012 35 1771-1777 Inhibitory Activity of Aralia continentalis Roots on Protein Tyrosine Phosphatase 1B and Rat Lens Aldose Reductase Hee Jin Jung, Hyun Ah Jung, Sam Sik Kang, Je-Hyun Lee, Yoon Sook Cho, Kyong Ho Moon, and Jae Sue Choi, Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxylignoceroyl amino)-8-octadecene-1,3,4-triol ÏàËÆ¶È:77.1% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxytricosanoyl amino)-8-octadecene-1,3,4-triol ÏàËÆ¶È:77.1% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxydocosanoyl amino)-8-octadecene-1,3,4-triol ÏàËÆ¶È:75.7% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxypalmitoyl amino)-8-octadecene-1,3,4-triol ÏàËÆ¶È:75% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Cerebroside ÏàËÆ¶È:74.2% Natural Product Sciences 2010 16 32-38 Phytochemical Studies on Lonicerae Flos (1) - Isolation of Iridoid Glycosides and other Constituents Lee, Eun-Ju; Lee, Joo-Young; Kim, Ju-Sun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ |

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