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1 .     6¦Â-hydroxymexrenone
     ÏàËÆ¶È:70.8%
Journal of Natural Products          2003          66          350-356
Biotransformations of the Cardiovascular Drugs Mexrenone and Canrenone
Carol L. Preisig, Jodi A. Laakso, Ursula M. Mocek, Ping T. Wang, Julio Baez, and Graham Byng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



2 .     Spironolactone
     ÏàËÆ¶È:70.8%
Steroids          2004          69          647-652
Novel spironolactone-analogs as impurities in spironolactone
Hua Chen, Xiao-Yi Wang, Zhong-Duo Yang, Yuan-Chao Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



3 .     16-(4-nitro-benzylidene)-5¦Á-androstan-3,17-dione
C26H31NO4     ÏàËÆ¶È:70.8%
Steroids          2011          76          709-723
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



4 .     (5S,8R,9S,10S,13S,14S,17S)-10,13-dimethylhexadecahydrospiro[cyclopenta[a]phenanthrene-17,2'-pyran]-3,6'(2H,3'H)-dione
C23H34O3     ÏàËÆ¶È:70.8%
Molecules          2013          18          914-933
Synthesis of 5¦Á-Androstane-17-spiro-¦Ä-lactones with a 3-Keto, 3-Hydroxy, 3-Spirocarbamate or 3-Spiromorpholinone as Inhibitors of 17¦Â-Hydroxysteroid Dehydrogenases
Guy Bertrand Djigou¨¦, B¨¦atrice Tch¨¦dam Ngatcha, Jenny Roy and Donald Poirier
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



5 .     3,3,12-Trihydroxy-7-ketocholanic acid
C24H36O5     ÏàËÆ¶È:70.8%
Molecules          2012          17          12357-12364
Two New Cholic Acid Derivatives from the Marine Ascidian-Associated Bacterium Hasllibacter halocynthiae
Sung Hun Kim, Yun Kyung Shin, Young Chang Sohn and Hak Cheol Kwon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



6 .     Phangininoxy B
C21H20O5     ÏàËÆ¶È:70.8%
Fitoterapia          2014          98          22-26
Norcassane- and cassane-type furanoditerpenoids from the seeds of Caesalpinia sappan
Hai-Feng Wu, Yin-Di Zhu, Zhong-Hao Sun, Jing-Quan Yuan, Hua Wei, Xiao-Po Zhang, Yu Tian, Jun-Shan Yang, Guo-Xu Ma, Xu-Dong Xu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



7 .     16-(4-nitro-benzylidene)-3¦Â-(4-Methylpiperazinyl)-5¦Á-androstan-17-one
C31H43N3O3     ÏàËÆ¶È:69.2%
Steroids          2011          76          709-723
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



8 .     compound 8
C25H34O5S     ÏàËÆ¶È:68%
Steroids          2004          69          647-652
Novel spironolactone-analogs as impurities in spironolactone
Hua Chen, Xiao-Yi Wang, Zhong-Duo Yang, Yuan-Chao Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



9 .     16-(4-nitro-benzylidene)-3¦Â-pyrrolidino-5¦Á-androstan-17-one
C30H40N2O3     ÏàËÆ¶È:68%
Steroids          2011          76          709-723
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



10 .     17¦Á-(Hemiglutaramido)-17¦Â-hydroxy-5¦Á-androstan-3-one
C26H41O5N     ÏàËÆ¶È:68%
Steroids          1997          62          603-620
Synthesis and characterization by 1H and 13C nuclear magnetic resonance spectroscopy of 17¦Á-cyano, 17¦Á-aminomethyl, and 17¦Á-alkylamidomethyl derivatives of 5¦Á-dihydrotestosterone and testosterone
Elisabeth Mappus, Christophe Chambon, Marc Rolland de Ravel, Catherine Grenot, Claude Y. Cuilleron
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



11 .     globostelletin G
C25H34O4     ÏàËÆ¶È:68%
Bioorganic & Medicinal Chemistry          2010          18          4639-4647
Globostelletins A¨CI, cytotoxic isomalabaricane derivatives from the marine sponge Rhabdastrella globostellata
Jin Li, Bo Xu, Jinrong Cui, Zhiwei Deng, Nicole J. de Voogd, Peter Proksch, Wenhan Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



12 .     briarellin A
C28H44O7     ÏàËÆ¶È:67.8%
Tetrahedron          1995          51          6869-6880
The briarellins, new eunicellin-based diterpenoids from a Caribbean gorgonian, Briareum asbestinum
Abimael D. Rodr¨ªguez, Oscar M. C¨®bar
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



13 .     daphnezomine L methyl ester
C23H35NO2     ÏàËÆ¶È:66.6%
Journal of Natural Products          2009          72          1669-1672
Alkaloids from the Leaves of Daphniphyllum subverticillatum
Chuan-Rui Zhang, Hong-Bing Liu, Teng Feng, Jian-Yong Zhu, Mei-Yu Geng, and Jian-Min Yue
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



14 .     phanginin F
C21H26O5     ÏàËÆ¶È:66.6%
Phytochemistry          2008          69          1242-1249
Phanginin A¨CK, diterpenoids from the seeds of Caesalpinia sappan Linn.
Orapun Yodsaoue,Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont,Suchada Chantrapromma, Hoong-Kun Fun,Akkharawit Kanjana-Opas
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



15 .     mexrenone
     ÏàËÆ¶È:66.6%
Journal of Natural Products          2003          66          350-356
Biotransformations of the Cardiovascular Drugs Mexrenone and Canrenone
Carol L. Preisig, Jodi A. Laakso, Ursula M. Mocek, Ping T. Wang, Julio Baez, and Graham Byng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



16 .     canrenone
     ÏàËÆ¶È:66.6%
Journal of Natural Products          2003          66          350-356
Biotransformations of the Cardiovascular Drugs Mexrenone and Canrenone
Carol L. Preisig, Jodi A. Laakso, Ursula M. Mocek, Ping T. Wang, Julio Baez, and Graham Byng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



17 .     11¦Á-hydroxymexrenone
C24H33O6     ÏàËÆ¶È:66.6%
Journal of Natural Products          2003          66          350-356
Biotransformations of the Cardiovascular Drugs Mexrenone and Canrenone
Carol L. Preisig, Jodi A. Laakso, Ursula M. Mocek, Ping T. Wang, Julio Baez, and Graham Byng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



18 .     ¦¤1,2-mexrenone
     ÏàËÆ¶È:66.6%
Journal of Natural Products          2003          66          350-356
Biotransformations of the Cardiovascular Drugs Mexrenone and Canrenone
Carol L. Preisig, Jodi A. Laakso, Ursula M. Mocek, Ping T. Wang, Julio Baez, and Graham Byng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



19 .     malyngamide P
C24H40ClNO5     ÏàËÆ¶È:66.6%
Journal of Natural Products          2000          63          1422-1424
Malyngamides O and P from the Sea Hare Stylocheilus longicauda
Winklet A. Gallimore and Paul J. Scheuer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ



20 .     anastomosacetal B
C27H42O4     ÏàËÆ¶È:66.6%
Journal of Natural Products          1996          59          1196-1199
Isolation of New Steroidal Hemiacetals from the Gorgonian Euplexaura anastomosans
Youngwan Seo, Jung-Rae Rho, Ki Woong Cho, and Jongheon Shin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-03-29 01:30:05
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