| ²é¿´: 236 | »Ø¸´: 1 | ||
pengbing99ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖúÒ»¸ö»¯ºÏÎ¶àл£¡ ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁCDCL3£¨125MHz£© 15.3,26.7,52.5,61.8,69.7,73.6,75.9,76.0,103.1,114.5,123.6,124.3,131.1,143.1,154.6,169.1 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸»ª¶«Ê¦·¶ÉúÎïѧ326·Ö£¬Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
071000ÉúÎïѧµ÷¼ÁÇóÖú
ÒѾÓÐ11È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ16È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
282£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ19È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
ÖпÆÔº×Ü·Ö315Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸¿ó´ó£¬²ÄÁϹ¤³Ìר˶314·Ö£¬0856¿Éµ÷¶¼¿ÉÒÔ
ÒѾÓÐ12È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
°ïæ²éÕÒÒ»¸ö»¯ºÏÎïµÄÃû³Æ
ÒѾÓÐ3È˻ظ´
ÇóÖú»¯ºÏÎï1¸ö£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÓÐÒ»¸ö»¯ºÏÎï´òÁ˺˴ÅÇâÆ×£¬¸÷λͬÈʰïæ·ÖÎöһϣ¬¿´ÊÇ·ñÊÇͼÖнṹʽ£¬Ð»Ð»£¡£¡
ÒѾÓÐ3È˻ظ´
¹ØÓÚÒ»¸öÓлú»¯ºÏÎïµÄÃüÃû
ÒѾÓÐ7È˻ظ´
ÄÄλÓпÉÒÔ²éѯ»¯ºÏÎï MSDSµÄÍøÕ¾£¬Ð»Ð»£¡
ÒѾÓÐ10È˻ظ´
Çó½âºË´ÅÇâÆ×£¡£¡£¡¶àл¶àл£¡£¡
ÒѾÓÐ19È˻ظ´
ÇóÖúÓлúС·Ö×Ó»¯ºÏÎïµ¥¾§ÅàÑøµÄÏêϸעÒâÊÂÏ
ÒѾÓÐ14È˻ظ´
ÓÐÈË¿ÉÒÔ°ïÎÒ·ÖÎöÒ»ÏÂÕâ¸ö»¯ºÏÎïµÄ¼«ÐÔ´óСÂð£¿
ÒѾÓÐ7È˻ظ´
Õâµ½µ×ÊÇÒ»¸ö»¯ºÏÎﻹÊÇÁ½¸ö»¯ºÏÎ¸ÃÔõô°ì£¿
ÒѾÓÐ4È˻ظ´
t9a ÇóÖúһ΢Æ×Êý¾Ý лл
ÒѾÓÐ10È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
Çë½ÌºìÍâÔÚ1650~1750Ö®¼ä³ö·å¹éÊô
ÒѾÓÐ13È˻ظ´
ÕâÁ½¸ö»¯ºÏÎïÄĸö¼«ÐÔ´ó£¬Ôõô·ÖÀë
ÒѾÓÐ9È˻ظ´
ÓÐÈ˰ïæ·ÖÎöÒ»ÏÂÕâÁ½¸ö»¯ºÏÎïµÄ¼«ÐÔ´óСÂð ¶àлÁË
ÒѾÓÐ22È˻ظ´
ÔõÑùÖªµÀÒ»¸ö»¯ºÏÎïµÄ¼«ÐÔ
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿200½ð±ÒÇóÖú·ÖÎö¼ì²âÁ½¸ö»¯ºÏÎïµÄ·½·¨£¡£¡
ÒѾÓÐ21È˻ظ´
¡¾ÇóÖú¡¿°ïæ±È½Ïһϼ¸ÖÖ»¯ºÏÎïÑõ»¯ÐÔÇ¿Èõ¹ØÏµ£¬·Ç³£¸Ðл£¡
ÒѾÓÐ3È˻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
pengbing99: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл£¡ 2015-05-11 15:38:20
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
pengbing99: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл£¡ 2015-05-11 15:38:20
|
1 . fragranoside K C16H22O8 ÏàËÆ¶È:75% Journal of Chinese Medicinal Materials 2014 37 603-606 Two new compounds from Dryopteris fragrans Zhang Yan-long, Li Jian-ping, Li Guo-Yu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 6-hydroxythymol 6-O-¦Â-D-glucopyranoside ÏàËÆ¶È:62.5% China Journal of Chinese Materia Medica 2005 30 °¢ÓýκʵµÄ»¯Ñ§³É·ÖÑо¿ Îâ ϼ, Ñî¾þɽ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Linalyl-O-¦Â-D-glucoside ÏàËÆ¶È:62.5% Archives of Pharmacal Research 2007 30 1067-1074 Lignan and terpene constituents from the aerial parts of saussurea pulchella Sang Un Choi, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Kang Ro Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 6-hydroxythymol 6-O-¦Â-D-glucopyranoside ÏàËÆ¶È:62.5% Journal of Shenyang Pharmaceutical University 2011 28 526-529 Isolation and identification of chemical constituents from the seeds of Trachyspermum ammi (L.) Sprague,a traditional uygur medicine MA, Qing-dong, LI, Guo-yu, WANG, Hang-yu, ZHANG, Ke, WANG, Jin-hui, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 6-(4-[¦Â-D-glucopyranoside-O-methylene]-1H-1,2,3-triazol-1-yl)-1,2-benzisothiazole-3-one-1,1-dioxide C16H18N4O9S ÏàËÆ¶È:62.5% Journal of Medicinal Chemistry 2014 57 3522-3531 Cyclic Secondary Sulfonamides: Unusually Good Inhibitors of Cancer-Related Carbonic Anhydrase Enzymes Janina Moeker, Thomas S. Peat, Laurent F. Bornaghi, Daniela Vullo, Claudiu T. Supuran, and Sally-Ann Poulsen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-05-11 15:06:36













»Ø¸´´ËÂ¥