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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
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liuxiaosa: ½ð±Ò+8, ¡ïÓаïÖú 2014-05-16 20:23:54
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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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâ
2Â¥2014-04-29 14:38:13
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