| ²é¿´: 382 | »Ø¸´: 1 | |||
szl1234Ìú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
19.437,23.513,24.411,40.220,49.875,66.544,78.291,125.944,128.372,136.384,164.827,197.790 DMSO |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ£¬³õÊԳɼ¨350Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ4È˻ظ´
323·Ö£¨¼ÆËã»úÊÓ¾õºÍ´óÄ£ÐÍÏîÄ¿£©ÄÜÖ±½ÓÉÏÊÖ
ÒѾÓÐ3È˻ظ´
311·Ö 22408 Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
320·ÖÈ˹¤ÖÇÄܵ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸Ö£´ó0705Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0703»¯Ñ§
ÒѾÓÐ10È˻ظ´
301Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
306·Ö²ÄÁÏÓ뻯¹¤Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
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
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
szl1234: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-04-15 11:26:40
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
szl1234: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-04-15 11:26:40
|
1 . 6,9-dihydroxy-4,7-megastigmadien-3-one C13H20O3 ÏàËÆ¶È:92.3% China Journal of Chinese Materia Medica 2005 30 1595-1597 Study on the chemical constituents in herb of Hypericum attenuatum DONG Jianyong, JIA Zhongjian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . blumenol A ÏàËÆ¶È:92.3% Chinese Journal of Natural Medicines 2008 6 112-115 Chemical Constituents of Alternanthera philoxeroides FAN Wen-Qian; XIONG Meng-Xiao; MA Zhuo; LI Qiong-Ya; LIU Yan-Wen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 6,9-dihydroxy-4,7-megastigmadien-3-one ÏàËÆ¶È:92.3% Asia-Pacific Traditional Medicine 2012 8 26-28 Chemical Constituents from Seeds of Hippophae Rhamnoides Liu Jiang, Xu Shuo, Song qiu-yue.He xiao-yan.Han Li, Huang Xue-shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . bluemenol A ÏàËÆ¶È:92.3% Journal of Shenyang Pharmaceutical University 2011 28 871-874 Isolation and identification of chemical constituents from Trichosanthes kirilowii Maxim. FAN, Xue-mei, CHEN, Gang, GUO, Li-na, LU, Xuan, SU, Shan-shan, PEI, Yue-hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . vomifoliol ÏàËÆ¶È:92.3% China Journal of Chinese Materia Medica 2013 38 1172-1182 Chemical consitituents from root of Isatis indigotica WANG Xiao-liang, CHEN Ming-hua, WANG Fang, BU Peng-bin, LIN Sheng, ZHU Cheng-gen, LI Yu-huan, JIANG Jian-dong, SHI Jian-gong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . arboreumine C25H40N2O5 ÏàËÆ¶È:91.6% Phytochemistry 2002 59 521-527 Antifungal amides from Piper arboreum and Piper tuberculatum Renata Vasques da Silva, Hosana M. Debonsi Navickiene, Massuo J. Kato,Vanderlan da S. Bolzani, Christiane I. M¨¦da, Maria Claudia M. Young,Maysa Furlan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 4,5-dihydroblumenol A ÏàËÆ¶È:91.6% China Journal of Chinese Materia Medica 2013 38 2321-2324 Chemical constituents from stems of Brucea mollis and their cytotoxic activity CHEN Hui, BAI Jian, FANG Zhen-feng, MA Shuang-gang, YU Shi-shan*, CHEN Xiao-guang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . blumenol A C13H20O3 ÏàËÆ¶È:84.6% Chemical & Pharmaceutical Bulletin 1992 40 3133-3137 Constituents of the Roots of Cynanchum bungei DECNE.Isolation and Structures of Four New Glucosides, Bunngeiside-A, -B, -C, and -D Jun LI,Shigetoshi KADOTA,Yukio KAWATA,Masao HATTORI,Guo-Jun XU and Tsuneo NAMBA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-14 18:36:06














»Ø¸´´ËÂ¥