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»¯ºÏÎïFR1 13C NMR(100MHz, C5D5N) ̼Æ×Êý¾ÝÈçÏ£º 17.16,17.29,17.70,18.04,19.44,24.56,25.11,26.84,27.37,27.56,29.70,29.76,34.00,38.88,38.96,40.25,40.90,42.61,42.79,48.28,48.33,48.72,55.04,56.42,69.05,73.18,84.32,128.41,140.38,181.02 »¯ºÏÎïFR40a 13C NMR(100MHz, DMSO-d6) 18.80,20.76,22.95,23.98,40.84,49.30,61.07,70.02,73.63,74.47,76.72,76.78,77.78,100.83,125.59,130.25,133.26,163.85,197.22 »¯ºÏÎïFR41 13C NMR(100MHz, DMSO-d6) 18.82,20.79,22.97,24.00,30.62,40.86,49.32,61.10,70.04,73.65,74.52,76.73,76.80,77.81,100.86,125.61,130.27,133.29,163.87,197.24,206.37 |
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yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
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1 . (6S,7E,9R)-roseoside C19H30O8 ÏàËÆ¶È:90.4% China Journal of Chinese Materia Medica 2005 30 983-986 The megastigman glycosides from herb of Potentilla multifida XUE Peifeng, LU Xinhua, WANG Bin, LIANG Hong, ZHAO Yuying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (+)-(6S,9R)-9-O-¦Â-D-Glucopyranosyloxy-6-hydroxy-3-oxo-¦Á-ionol C19H30O8 ÏàËÆ¶È:90.4% Chemistry of Natural Compounds 2011 Vol. 47, No. 2 272-274 CHEMICAL CONSTITUENTS FROM PINE NEEDLES OF Cedrus deodara Jun Min Zhang, Xiao Feng Shi, Qu Huan Ma,Fu Jiang He, Bin Fan,Dong Dong Wang,and Dong Yan Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . vomifoliol ¦Â-D-glucopyranoside ÏàËÆ¶È:90.4% Phytochemistry 1990 29 161-164 Vomifoliol 1-O-¦Â-d-xylopyranosyl-6-O-¦Â-d-glucopyranoside: A disaccharide glycoside from apple fruit Wilfried Schwab,Peter Schreier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (6S,9R)-roseoside ÏàËÆ¶È:90.4% China Journal of Chinese Materia Medica 2010 35 3156-3160 Chemical constituents from roots of Pueraria lobata LI Guohui; ZHANG Qingwen; WANG Yitao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (6S,9R)-roseoside ÏàËÆ¶È:90.4% Journal of Shenyang Pharmaceutical University 2009 26 614-616 Chemical constituents from Rernel of Castanea mollissima Blume(IV) LONG Zhi-min, WU Li-jun, SUN Bo-hang, HUANG Jian, GAO Hui-yuan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (6S,9R)-roseoside C19H30O8 ÏàËÆ¶È:90.4% Journal of Shenyang Pharmaceutical University 2008 25 956-959 Megastigmane glucosides from the stems and leaves of the Physalis alkekengi L. var. f rancheti QIU Li, LIU Hong-xia, JIANG Zhi-hu, QIN Geng-yao, CHEN Li-xia, QIU Feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (6S,9R)-roseoside ÏàËÆ¶È:90.4% Natural Product Research and Development 2005 17 440-443 Studies on the Antibacterial Chemical Components of Senecio cannabifolius Less.(¢ó) WU Bin; LI Wen; LIN Wen-hui; GAO Hui-yuan; WU Li-jun*; KIM Chul-sa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (6S,9R)-roseoside ÏàËÆ¶È:90.4% China Journal of Chinese Materia Medica 2012 37 2408-2412 Chemical constituents from Hypericum perforatum MA Jie; YANG Jianbo; JI Tengfei; WANG Aiguo; SU Yalun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (6S,9R)-³¤ÊÙ»¨ÌÇÜÕ ÏàËÆ¶È:90.4% China Journal of Chinese Materia Medica 2011 36 1779-1781 Polar constituents ofMosla Chinensis SH, EN, Juanjuan, ZHANG, Dongming, LIU, Hua, LUO, Yongming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (6S,9R)-6-hydroxy-3-oxo-¦Á-ionol-9-O-¦Â-D-glucopyranoside ÏàËÆ¶È:90.4% Chinese Traditional and Herbal Drugs 2014 45 2602-2606 Chemical constituents in n-butanol extract from pine needles of Cedrus deodara LI Shi, LIU Dong-yan, SHI Xiao-feng, LEI Yan-ping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2015-05-01 10:57:09
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
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- Ìû×Ó: 2773
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- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
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fengfajin(¶¹¸ç´ú·¢): ½ð±Ò+30 2015-05-04 14:35:43
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fengfajin(¶¹¸ç´ú·¢): ½ð±Ò+30 2015-05-04 14:35:43
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1 . tormentic acid ÏàËÆ¶È:100% Planta Medica 1992 58 227 Tormentic Acid and 2¦Á-Hydroxyursolic Acid from Arnebia euchroma M.-H.Yang,G.Blunden,M.J.O'Neill,and J.A.Lewis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 2¦Á,19¦Á-¶þôÇ»ùÎÚË÷Ëá C30H48O5 ÏàËÆ¶È:100% Acta Botanica Yunnanica 1998 20(2) 241-243 The Chemical Constituents of Isodon lophanthoides in Guizhou CHEN Xing-Liang YANG Xiu-Ping,HOU Ai-J un J IANGBei,L IN Zhong-Wen SUN Han-Dong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . tormentic acid C30H48O5 ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1989 37 648-651 Cytotoxic Triterpenes from a Chinese Medicine, Goreishi Atsushi NUMATA,Peiming YANG,Chika TAKAHASHI,Ryoko FUJIKI,Michiko NABAE and Eiichi FUJITA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . tormentic acid ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2009 34 2610-2612 Chemical constituents of roots of Boehme rianivea XU Qiongming, CHEN Guoqing, FAN Jinying, ZHANGMengjia, LIXia, YANG Shilin, LIxiaoran Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . tormentic acid C30H48O5 ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2006 31 1875-1879 Triterpenes from herb of Potentilla chinesis LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . tormentic acid ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2005 30 1833-1836 Triterpenes from root of Rhaponticum uniflorum ZHANG Yonghong, ZHANG Jiangang, XIE Jieming, CHEN Gelin, CHENG Dongliang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . tomentic acid ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 1997 22 680-682 Chemical studies on Campylotropis hirtella (Franch. Schindl.) Lu Xuezhao , Xu Wenhao and Shen Jiaxiang, Han Guiqiu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . tomentic acid ÏàËÆ¶È:100% Natural Product Sciences 2005 11 196-198 Constituents of the Aerial Parts of Agrimonia pilosa An, Ren-Bo; Kim, Hyun-Chul; Jeong, Gil-Saeng; Oh, Seung-Hwan; Oh, Hyun-Cheol; Kim, Youn-Chul Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 2¦Á,3¦Â,19¦Á-trihydroxyurs-12-ene-28-oic acid(tormentic acid) ÏàËÆ¶È:100% Korean Journal of Pharmacognosy 1996 27(4) 389-396 Constituents of Spiraea prunifolia var. simpliciflora Lee, Eun-Hee; Chung, Soon-Ok; Kim, Chong-Won; Woo, Mi-Hee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . tormentic acid ÏàËÆ¶È:100% Korean Journal of Pharmacognosy 1991 22(3) 166-170 Studies on the Constituents of Lycopus lucidus (II) Do, Jae-Chul; Chai, Joo-Young; Son, Jong-Keun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-05-01 10:52:27
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
|
1 . (6S,7E,9R)-roseoside C19H30O8 ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2005 30 983-986 The megastigman glycosides from herb of Potentilla multifida XUE Peifeng, LU Xinhua, WANG Bin, LIANG Hong, ZHAO Yuying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (+)-(6S,9R)-9-O-¦Â-D-Glucopyranosyloxy-6-hydroxy-3-oxo-¦Á-ionol C19H30O8 ÏàËÆ¶È:100% Chemistry of Natural Compounds 2011 Vol. 47, No. 2 272-274 CHEMICAL CONSTITUENTS FROM PINE NEEDLES OF Cedrus deodara Jun Min Zhang, Xiao Feng Shi, Qu Huan Ma,Fu Jiang He, Bin Fan,Dong Dong Wang,and Dong Yan Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . vomifoliol ¦Â-D-glucopyranoside ÏàËÆ¶È:100% Phytochemistry 1990 29 161-164 Vomifoliol 1-O-¦Â-d-xylopyranosyl-6-O-¦Â-d-glucopyranoside: A disaccharide glycoside from apple fruit Wilfried Schwab,Peter Schreier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (6S,9R)-roseoside ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2010 35 3156-3160 Chemical constituents from roots of Pueraria lobata LI Guohui; ZHANG Qingwen; WANG Yitao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (6S,9R)-roseoside ÏàËÆ¶È:100% Journal of Shenyang Pharmaceutical University 2009 26 614-616 Chemical constituents from Rernel of Castanea mollissima Blume(IV) LONG Zhi-min, WU Li-jun, SUN Bo-hang, HUANG Jian, GAO Hui-yuan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (6S,9R)-roseoside C19H30O8 ÏàËÆ¶È:100% Journal of Shenyang Pharmaceutical University 2008 25 956-959 Megastigmane glucosides from the stems and leaves of the Physalis alkekengi L. var. f rancheti QIU Li, LIU Hong-xia, JIANG Zhi-hu, QIN Geng-yao, CHEN Li-xia, QIU Feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-05-01 10:55:26













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