| ²é¿´: 300 | »Ø¸´: 1 | ||
190824656ľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×Ç󻯺ÏÎï½á¹¹
|
| ̼Æ×Êý¾Ý£º18.4, 23.0, 25.7, 30.9, 31.6, 32.3, 34.3, 36.6, 37.5, 43.1, 43.1, 49.8, 54.5, 57.6, 60.4, 67.0, 70.4, 108.5, 114.6, 131.6, 132.5, 139.9, 159.6, 175.5, 211.6 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ9È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ10È˻ظ´
Ò»Ö¾Ô¸211£¬0703»¯Ñ§305·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Ç󻯺ÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹£¨¹²4¸ö£©
ÒѾÓÐ5È˻ظ´
Çó΢ÆÕ½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
MestReNovaÎÞ·¨½øÐл¯ºÏÎï½á¹¹ÇâÆ×Ô¤²â
ÒѾÓÐ12È˻ظ´
Çó΢Æ×¼ìË÷»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÍÆ¼ö¹ØÓÚ»¯ºÏÎï½á¹¹Óë»îÐÔ¹ØÏµµÄÆÚ¿¯
ÒѾÓÐ4È˻ظ´
ÇóÖúÓÃCDÆ×½âÎöÒ»¸öÄ¾Ö¬ËØÀ໯ºÏÎïµÄ¾ø¶Ô¹¹ÐÍ
ÒѾÓÐ7È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇëÎÊÓÐûÓÐÒ»¸ö»¯ºÏÎï±ê×¼Æ×ͼ½âÎöÊý¾Ý¿â£¿
ÒѾÓÐ5È˻ظ´
danil1288
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 96 (³õÖÐÉú)
- ½ð±Ò: 4099.5
- É¢½ð: 14
- ºì»¨: 2
- Ìû×Ó: 405
- ÔÚÏß: 109.3Сʱ
- ³æºÅ: 779961
- ×¢²á: 2009-05-26
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©Ò©ÐÔÀíÂÛ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
190824656: ½ð±Ò+15 2013-08-28 11:09:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
190824656: ½ð±Ò+15 2013-08-28 11:09:59
|
²éѯ½á¹û£º¹²²éµ½249¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 1 C24H31NO7 ÏàËÆ¶È:96% The Journal of Antibiotics 1996 49 693-696 A Cholesteryl Ester Transfer Protein Inhibitor from an Insect-associated Fungus JULIE C. LEE, STEPHEN J. COVAL, JON CLARD Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . apiosporamide C24H31NO6 ÏàËÆ¶È:80% Journal of Natural Products 1994 Vol 57 1696 Apiosporamide, a New Antifungal Agent from the Coprophilous Fungus Apiospora montagnei Ali A. Alfatafta, James B. Gloer, James A. Scott, David Malloch Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 12-epi-15-acetylnapelline C24H35NO4 ÏàËÆ¶È:60% Planta Medica 2005 71 1073-1076 Three New Diterpene Alkaloids from the Roots of Aconitum nagarum var.lasiandrum Fan Zhang , Shu-Lin Peng , Xun Liao , Kai-Bai Yu , Li-Sheng Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (5'R)-17¦Â-[2-phenyl)-4,5-dihydrooxazol-5-yl]androst-5-en-3¦Â-ol C29H41NO2 ÏàËÆ¶È:57.6% Steroids 2009 74 1025-1032 Steroselective synthesis of some steroidal oxazolines, as novel potential inhibitors of 17¦Á-hydroxylase-C17,20-lyase D¨®ra Ondr¨¦, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (5'R)-17¦Â-[2-(4-fluorophenyl)-4,5-dihydrooxazol-5-yl]androst-5-en-3¦Â-ol C28H36FNO2 ÏàËÆ¶È:57.6% Steroids 2009 74 1025-1032 Steroselective synthesis of some steroidal oxazolines, as novel potential inhibitors of 17¦Á-hydroxylase-C17,20-lyase D¨®ra Ondr¨¦, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (5'R)-17¦Â-[2-(2-chlorophenyl)-4,5-dihydrooxazol-5-yl]androst-5-en-3¦Â-ol C28H36ClNO2 ÏàËÆ¶È:57.1% Steroids 2009 74 1025-1032 Steroselective synthesis of some steroidal oxazolines, as novel potential inhibitors of 17¦Á-hydroxylase-C17,20-lyase D¨®ra Ondr¨¦, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (rel 5S,6R,8R,9R,10S,13S,15S,16S)-6-acetoxy-9,13;15,-16-diepoxy-15,16-dimethoxylabdane ÏàËÆ¶È:56% Journal of Natural Products 1999 62 1532-1537 Diterpenes from the Fruits of Vitex rotundifolia Masateru Ono, Megumi Yamamoto, Chikako Masuoka, Yasuyuki Ito, Masami Yamashita, and Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . finetianine C21H29NO3 ÏàËÆ¶È:56% Planta Medica 2005 71 1073-1076 Three New Diterpene Alkaloids from the Roots of Aconitum nagarum var.lasiandrum Fan Zhang , Shu-Lin Peng , Xun Liao , Kai-Bai Yu , Li-Sheng Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 7,12-diketolithocholic acid ÏàËÆ¶È:56% Steroids 2006 71 469-475 Regio- and stereoselective reductions of dehydrocholic acid Giancarlo Cravotto, Arianna Binello, Luisa Boffa, Ornelio Rosati, Marco Boccalini, Stefano Chimichi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . apiosporamide C24H31NO6 ÏàËÆ¶È:56% Journal of Natural Products 1994 Vol 57 1696 Apiosporamide, a New Antifungal Agent from the Coprophilous Fungus Apiospora montagnei Ali A. Alfatafta, James B. Gloer, James A. Scott, David Malloch Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 5e C25H32O3 ÏàËÆ¶È:56% Chemical Journal of Chinese Universities 2006 27 2101-2105 Synthesis and Anti-tumor Activities of a Series of Novel Tricycle Diterpenes XIONG Yi,WANG Kui-Wu,PAN Yuan-Jiang, SUN Hong-Xiang Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-08-27 21:48:59














»Ø¸´´ËÂ¥