| ²é¿´: 183 | »Ø¸´: 1 | |||
liuxiaosaľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
| 12.6,14.4,17.3,22.3,23.7,25.2,26.9,30.3,30.5,30.6,30.8,31.6,31.7,33.5,35.3,39.3,41.4,43.9,46.6,57.5,68.3,76.5,76.8 |
» ²ÂÄãϲ»¶
¶þ´Îµ÷¼ÁÇóÀÏʦÊÕÁô
ÒѾÓÐ3È˻ظ´
349ѧ¿Æ»¯Ñ§045106Çóµ÷¼Á£¬»¯Ñ§Àà¶¼¿ÉÒÔ
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸0807 ÊýÒ»Ó¢Ò» 313 ÓÐûÓжþÂÖµ÷¼Á
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á£¬262»úеר˶
ÒѾÓÐ5È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
0860004 Çóµ÷¼Á 309·Ö
ÒѾÓÐ3È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ20È˻ظ´
µ÷¼Á
ÒѾÓÐ11È˻ظ´
¿¼Ñе÷¼Á-²ÄÁÏÀà-284
ÒѾÓÐ13È˻ظ´
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ13È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¹òÇ󣬷dz£¸Ðл£¡
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ºÃÐÄÈËÇëÖ¸µãÒ»ÏÂÔõôÕâô¶à̼
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻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´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
liuxiaosa: ½ð±Ò+8, ¡ïÓаïÖú 2014-05-16 20:23:54
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
liuxiaosa: ½ð±Ò+8, ¡ïÓаïÖú 2014-05-16 20:23:54
|
²éѯ½á¹û£º¹²²éµ½1646¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5R-cholan-2¦Â,3R,24-tryl-2,3,24-sodium trisulfate C24H39Na3O12S3 ÏàËÆ¶È:69.5% Journal of Medicinal Chemistry 2011 54 4590-4599 Total Synthesis and Pharmacological Characterization of Solomonsterol A, a Potent Marine Pregnane-X-Receptor Agonist Endowed with Anti-Inflammatory Activity Valentina Sepe, Raffaella Ummarino, Maria Valeria D¡¯Auria, Andrea Mencarelli, Claudio D¡¯Amore, Barbara Renga, Angela Zampella, and Stefano Fiorucci Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 17¦Â-(2',5'-Dihydro-5'-oxo-3'-furyl)-5¦Á-androstane-3¦Â,5,6¦Â-triol C23H34O6 ÏàËÆ¶È:69.5% Organic Magnetic Resonance 1977 9 439-464 13C n.m.r. spectra of steroids ¡ªa survey and commentary J. W. Blunt and J. B. Stothers Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-araguspongine L C28H50O5N2 ÏàËÆ¶È:67.8% Journal of Natural Products 2002 65 1782-1785 Araguspongines K and L, New Bioactive Bis-1-oxaquinolizidine N-Oxide Alkaloids from Red Sea Specimens of Xestospongia exigua Khaled Y. Orabi,Khalid A. El Sayed, Mark T. Hamann, D. Chuck Dunbar, Mansour S. Al-Said,Tatsuo Higa,and Michelle Kelly Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . clerod-14-epoxy-3¦Á,4¦Â,13¦Î-triol ÏàËÆ¶È:67.8% Natural Product Research 2002 16 323-327 Antifeedant Activity of Metabolites from Viguiera Tucumanensis Clarisa E. Vaccarini; Sara M. Palacios; Karina M. Meragelman; Virginia E. Sosa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (24R)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol C29H52O3 ÏàËÆ¶È:67.8% Journal of Natural Products 1991 Vol 54 1570 3¦Â,5¦Á,6¦Â-Trihydroxylated Sterols with a Saturated Nucleus from Two Populations of the Marine Sponge Cliona copiosa Giacomo Notaro, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . zahramycin A C28H48O3 ÏàËÆ¶È:67.8% Zeitschrift f¨¹r Naturforschung B 2013 68 939-945 Zahramycins A-B, Two New Steroids from the Coral Sarcophyton trocheliophorum Mohamed Shaaban, Mohamed A. Ghani and Khaled A. Shaaban Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5¦Á-cholestane-3¦Â,5,6¦Â-triol C27H4HO3 ÏàËÆ¶È:66.6% Journal of Natural Products 1991 Vol 54 1570 3¦Â,5¦Á,6¦Â-Trihydroxylated Sterols with a Saturated Nucleus from Two Populations of the Marine Sponge Cliona copiosa Giacomo Notaro, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 5¦Á-cholestane-3¦Â,5,6¦Â,15¦Á,16¦Â-pentaol 16-sulfate ÏàËÆ¶È:66.6% Journal of Natural Products 1995 Vol 58 653-671 Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Âó½ÇçÞ-3¦Â,5¦Á,6¦Â-Èý´¼ ÏàËÆ¶È:66.6% Chinese Journal of Marine Drugs 2010 29(2) 6-9 Secondary metabolites from marine actinomycete Strep tomyces sp. ( No. 172221) MA Jing-jing, T ANG Jin-shan, GAO Hao, HONG Kui, ZHOU Guang-xiong, YAO Xin-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . chalinulasterol C24H39ClS2O8Na2 ÏàËÆ¶È:66.6% Marine Drugs 2012 10 1383-1390 Chalinulasterol, a Chlorinated Steroid Disulfate from the Caribbean Sponge Chalinula molitba. Evaluation of Its Role as PXR Receptor Modulator Roberta Teta, Gerardo Della Sala, Barbara Renga, Alfonso Mangoni, Stefano Fiorucci and Valeria Costantino Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . muriflasteroid C C27H46O3 ÏàËÆ¶È:66.6% Steroids 2013 78 108-114 3¦Â,5¦Á,6¦Â-Oxygenated sterols from the South China Sea gorgonian Muriceopsis flavida and their tumor cell growth inhibitory activity and apoptosis-inducing function Tao-Fang Liu, Xin Lu, Hua Tang, Min-Min Zhang, Pan Wang, Peng Sun, Zhi-Yong Liu, Zeng-Lei Wang, Ling Li, Yao-Cheng Rui, Tie-Jun Li, Wen Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 12-Thi¦Á-3¦Á,7¦Á-dihydroxy-5¦Â-cholan-12,12-dioxide-24-ol C23H40O5S ÏàËÆ¶È:65.2% Steroids 2011 76 324-330 Synthesis of 12-oxa, 12-aza and 12-thia cholanetriols Malika Ibrahim-Ouali, Khalil Hamze, Luc Rocheblave Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (3aR,5S,8aR,9aR)-3a,5,6,7,8,8a,9,9a-Octahydro-5,8a-dimethyl-3-[(undecylamino)methyl]naphtho-[2,3-b]furan-2(3H)-one C26H45NO2 ÏàËÆ¶È:65.2% Chemistry & Biodiversity 2010 7 1681-1697 Structure¨CActivity Relationship Studies on Derivatives of Eudesmanolides from Inula helenium as Toxicants against Aedes aegypti Larvae and Adults Charles L. Cantrell, Julia W. Pridgeon, Frank R. Fronczek and James J. Becnel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 20¦Â-Acetylamino-11¦Á-hydroxy-5¦Á-pregnan-3-one ÏàËÆ¶È:65.2% Steroids 1998 63 484-495 Microbial hydroxylation of acetylaminosteroids HerbertL Holland, Gingipalli Lakshmaiah, PeterL Ruddock Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 19-nor-5¦Â,17¦Á-pregnane-3¦Â,17¦Â-diol C20H34O2 ÏàËÆ¶È:65.2% Australian Journal of Chemistry 2003 56 829-838 Equine Metabolites of Norethandrolone: Synthesis of a Series of 19-Nor-17¦Á-pregnanediols and 19-Nor-17¦Á-pregnanetriols Andrew R. McKinney, Damon D. Ridley and Peter Turner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâ |
2Â¥2014-04-29 14:38:13













»Ø¸´´ËÂ¥