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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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