| ²é¿´: 348 | »Ø¸´: 1 | ||
ËÉÂÜ·çľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú S2G425 13C-NMR(CDCl3) £¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
|
|
S2G425 13C-NMR(CDCl3) 14.1,32.8,52.5,56.0,56.0,56.2,79.9,101.0,105.7,108.1,108.9,109.3,117.1, 123.0,123.5,127.1,131.5,132.8,135.0,139.7,141.2,146.3,147.4,172.3,187.1 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á£¬Ò»Ö¾Ô¸²ÄÁÏ¿ÆÑ§Ó빤³Ì985£¬365·Ö£¬
ÒѾÓÐ5È˻ظ´
271Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
0854µ÷¼Á
ÒѾÓÐ7È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ44È˻ظ´
085410 273Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁÏ¿¼Ñе÷¼Á
ÒѾÓÐ25È˻ظ´
²ÄÁϹ¤³Ì281»¹Óе÷¼Á»ú»áÂð
ÒѾÓÐ11È˻ظ´
303Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
290µ÷¼ÁÉúÎï0860
ÒѾÓÐ14È˻ظ´
ũѧ0904 312Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Ò»¸ö(С·Ö×Ó)£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
10£¬Î¢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡£¨E7-2-3-2£©
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
»¯ºÏÎï΢Æ×ÇóÖú£¬ÔÚÏߵȣ¬Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¸Ð¼¤£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл´ó¼Ò
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»df12
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ËÉÂÜ·ç: ½ð±Ò+8 2015-05-17 11:48:25
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ËÉÂÜ·ç: ½ð±Ò+8 2015-05-17 11:48:25
|
1 . Futoquinol ÏàËÆ¶È:84% Phytochemistry 1993 32 445-448 Lignans and neolignans from Piper schmidtii Om Dutt Tyagi, Søren Jensen, Per M. Boll, Nawal K. Sharma, Kirpal S. Bisht, Virinder S. Parmar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . futoquinol ÏàËÆ¶È:84% Journal of Chinese Medicinal Materials 2012 35 53-56 Study on the Bioactive Constituents of Piper wallichii ZHAO Guo-wei, XIA Wen, CHEN Ping, HAN En-ji, XIANG Lan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . futoquinol C21H22O5 ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2005 36 184-185 º£·çÌٵĻ¯Ñ§³É·ÖÑо¿(¢ñ) ÈηçÖ¥,ÕÅÀö,Å£¹ðÔÆ,Áõ¸ÕÈþ,¶Îº£Çå Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . hancinone D C21H22O5 ÏàËÆ¶È:72% Acta Pharmaceutica Sinica 1989 Vol 24 438-443 THE ISOLATION AND IDENTIFICATION OF PAF INHIBITORS FROM PIPER WALLICHII (MIQ.) HAND-MAZZ AND P. HANCEI MAXIM. GQ Han; LH Wei; CL Li; L Qiao; YZ Jia and QT Zheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Isodihydrofutoquinol-B ÏàËÆ¶È:72% Phytochemistry 1993 32 445-448 Lignans and neolignans from Piper schmidtii Om Dutt Tyagi, Søren Jensen, Per M. Boll, Nawal K. Sharma, Kirpal S. Bisht, Virinder S. Parmar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . piperkadsin A C21H24O5 ÏàËÆ¶È:68% Journal of Natural Products 2006 69 842-844 Anti-inflammatory Neolignans from Piper kadsura Lie-Chwen Lin, Chien-Chang Shen, Yuh-Chiang Shen, and Tung-Hu Tsai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Isodihydrofutoquinol-A ÏàËÆ¶È:68% Phytochemistry 1993 32 445-448 Lignans and neolignans from Piper schmidtii Om Dutt Tyagi, Søren Jensen, Per M. Boll, Nawal K. Sharma, Kirpal S. Bisht, Virinder S. Parmar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . isodihydrofutoquinol B C21H24O5 ÏàËÆ¶È:64% Natural Product Research 1994 4 35-42 Neolignans from Indian Piper Species: Structure of Hookerinone A, a novel Neolignan P. Pradhan; S. J. Desai; L. P. Badheka; A. Banerji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . wallichinine C22H26O5 ÏàËÆ¶È:64% Acta Pharmaceutica Sinica 1989 Vol 24 438-443 THE ISOLATION AND IDENTIFICATION OF PAF INHIBITORS FROM PIPER WALLICHII (MIQ.) HAND-MAZZ AND P. HANCEI MAXIM. GQ Han; LH Wei; CL Li; L Qiao; YZ Jia and QT Zheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-05-16 20:51:44













»Ø¸´´ËÂ¥