| ²é¿´: 264 | »Ø¸´: 1 | ||||
jessiegao07½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú£¬·Ç³£¸Ðл
|
|
13C NMR (cdcl3) 12.65,13.39,16.57,20.18,21.69,23.42,26.33,29.32,29.95,33.91,38.51,38.89,45.08,52.16,58.19,63.99,78.77,92.11,134.58,143.90,169.76,195.30 ·Ç³£·Ç³£¸Ðл£¡ |
» ²ÂÄãϲ»¶
µ÷¼Á
ÒѾÓÐ16È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ23È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁÏר˶µ÷¼Á
ÒѾÓÐ10È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
278Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
259Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬¸ßÊÖÏàÖú°¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖúлл
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
±ÏÒµ¼±ÐèÊý¾Ý£¬Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jessiegao07: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£·Ç³£¸Ðл£¡ 2013-07-22 19:55:30
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jessiegao07: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£·Ç³£¸Ðл£¡ 2013-07-22 19:55:30
|
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½380¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-15-Acetoxy-5,6-epoxylathyr-12-en-3-ol-14-one C22H32O5 ÏàËÆ¶È:100% Journal of Natural Products 2011 74 1221-1229 Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3,15-Diacetoxy-5,6-epoxylathyr-12-en-14-one C24H34O6 ÏàËÆ¶È:87.5% Journal of Natural Products 2011 74 1221-1229 Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 15-O-acetyl-3-O-iso-butyryljolkinol-5¦Â,6¦Â-oxide ÏàËÆ¶È:80.7% Phytochemistry 1983 22 1791-1795 Lathyrane type diterpenoid esters from Euphorbia characias Edgar H. Seip, Erich Hecker Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Acetoxy-5,6-epoxylathyr-12-en-15-ol-14-one C22H32O5 ÏàËÆ¶È:72.7% Journal of Natural Products 2011 74 1221-1229 Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . latilagascene B C29H36O6 ÏàËÆ¶È:66.6% Planta Medica 2006 72 162-168 New Macrocyclic Lathyrane Diterpenes, from Euphorbia lagascae, as Inhibitors of Multidrug Resistance of Tumour Cells No¨¦lia Duarte,Nora Gy¨¦m¨¢nt,Pedro M. Abreu,Joseph Moln¨¢r,Maria-Jos¨¦ U. Ferreira Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Acetoxy-15-benzoyloxy-5,6-epoxylathyr-12-en-14-one C29H36O6 ÏàËÆ¶È:66.6% Journal of Natural Products 2011 74 1221-1229 Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (+)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Benzoyloxy-5,6-epoxylathyr-12-en-15-ol-14-one C27H34O5 ÏàËÆ¶È:60% Journal of Natural Products 2011 74 1221-1229 Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 4 C29H36O6 ÏàËÆ¶È:59.2% Tetrahedron 2004 60 5025-5030 New tri- and tetracyclic diterpenes from Euphorbia villosa Andrea Vasas, Judit Hohmann, Peter Forgo, P¨¢l Szab¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 4 C29H36O6 ÏàËÆ¶È:59.2% Tetrahedron 2004 60 5025-5030 New tri- and tetracyclic diterpenes from Euphorbia villosa Andrea Vasas, Judit Hohmann, Peter Forgo, P¨¢l Szab¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 14 ÏàËÆ¶È:59.0% European Journal of Organic Chemistry 1993 1993 491-495 Studies on the Constituents of the Stems of Tinospora tuberculata, IV. Isolation and Structure Elucidation of the Five New Furanoid Diterpene Glycosides Borapetoside C¨CG Naomichi Fukuda, Michiko Yonemitsu and Takeatsu Kimura Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (-)-(5E,12E,2S,3S,4S,9S,11S,15R)-3,15-Diacetoxylathyra-5,12-dien-14-one C24H34O5 ÏàËÆ¶È:58.3% Journal of Natural Products 2011 74 1221-1229 Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . rel-(3'R)-3',8'-dihydrotokinolide B C24H30O4 ÏàËÆ¶È:56.5% Natural Product Research 2011 Vol. 25, No. 13 1234-1242 Phthalides and other constituents from Ligusticum porteri; sedative and spasmolytic activities of some natural products and derivatives Alejandra Le¨®n, Rub¨¦n A. Toscano, Jaime Tortoriello and Guillermo Delgado Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . methyl 15-acetoxy(10),13E-ent-halimadien-18-oate ÏàËÆ¶È:56.5% Phytochemistry 1987 26 1077-1079 Diterpenoids from halimium viscosum L.G. Urones,J. De Pascual Teresa,L.S¨¢nchez Marcos,D. D¨ªez Mart¨ªn,N. Mart¨ªn Garrido,R.Alfayate Guerra Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . methyl-(13S,14S)-epoxy-15-acetoxy-1(10)-ent-halimen-18-oate ÏàËÆ¶È:56.5% Phytochemistry 1990 29 1247-1251 ent-Halimane diterpenes from Halimium viscosum Julio G. Urones,Isidro S¨¢nchez Marcos,MJos¨¦ Sexmero Cuadrado,Pilar Basabe,Anna M. Lithgow Bertelloni Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . methyl-(13R,14R)-epoxy-15-acetoxy-1(10)-ent-halimen-18-oate ÏàËÆ¶È:56.5% Phytochemistry 1990 29 1247-1251 ent-Halimane diterpenes from Halimium viscosum Julio G. Urones,Isidro S¨¢nchez Marcos,MJos¨¦ Sexmero Cuadrado,Pilar Basabe,Anna M. Lithgow Bertelloni Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 20-acetoxy-pinusolide C23H32O6 ÏàËÆ¶È:56.5% Phytochemistry 1985 24 2041-2046 Diterpenes from the seed of Sciadopitys verticillata Shinichi Hasegawa, Yoshiyuki Hirose Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (22E)-24¦Á-methyl-ergost-6,22(23)-diene-5¦Á,8¦Á-epidioxy-3¦Â-ol C28H44O3 ÏàËÆ¶È:55.5% Indian Journal of Chemistry 1996 35B 806-809 Lipid constituents of marine sponge Suberites carnosus Prabhu D Mishra, Solimabi Wahidulla, L D Souza & S Y Kamat Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (+)-(12E,2S,3S,4R,5R,6R,9S,11S,15R)-3-Cinnamoyloxy-5,6-epoxylathyr-12-en-15-ol-14-one C29H36O5 ÏàËÆ¶È:55.5% Journal of Natural Products 2011 74 1221-1229 Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Yanru Li, Liang Xiong, Sujuan Wang, Ling Wang, Yongchun Yang, Ying Guo, Hua Sun, Xiaoliang Wang, and Jiangong Shi Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-07-22 19:38:57














»Ø¸´´ËÂ¥