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1 . 5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Á-dihydroxy-5¦Â-cholan-24-oate C51H81NO6 ÏàËÆ¶È:70.5% Steroids 2009 74 424-434 Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Â-dihydroxy-5¦Â-cholan-24-oate C51H81NO6 ÏàËÆ¶È:70.5% Steroids 2009 74 424-434 Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,6¦Á-dihydroxy-5¦Â-cholan-24-oate C51H81NO6 ÏàËÆ¶È:70.5% Steroids 2009 74 424-434 Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (3S,20S)-20-[(1R,S)-(1,2-dimethyl-propylamino)-methyl]-pregn-7-en-3-ol C24H39NO ÏàËÆ¶È:67.3% Bioorganic & Medicinal Chemistry 2009 17 8123-8137 Side chain azasteroids and thiasteroids as sterol methyltransferase inhibitors in ergosterol biosynthesis Delphine Renard, Johann Perruchon, Martin Giera, Jörg M¨¹ller, Franz Bracher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . N-hydroxysolasodine C27H43NO3 ÏàËÆ¶È:65.2% Phytochemistry 1992 31 1837-1839 N-Hydroxysolasodine from Solanum robustum Helmut Ripperger, Andrea Porzel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 7-hydroxysitosteryl-3-O-¦Â-D-glucopyranoside tetraacetate ÏàËÆ¶È:65.2% Phytochemistry 1991 30 3383-3387 Steroids and triterpenoids from Rosa laevigata Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . glucoraphenin ÏàËÆ¶È:65.2% Natural Product Research and Development 2010 22 58-59 Studies on the Chemical Constituents of Cirsium henryi ZHANG Yue; RUAN Han-li; ZHANG Yong-hui; PI Hui-fang; WU Ji-zhou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (cis)-2-(4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl)cyclohexyl (3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate ÏàËÆ¶È:64.5% Bioorganic & Medicinal Chemistry 2010 18 8194-8203 Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . N-(Cholest-5-en-3¦Â-yl)-3¦Â-hydroxyandrost-5-ene-17¦Â-carboxamide C47H75NO2 ÏàËÆ¶È:63.8% Steroids 2009 74 88-94 Steroids linked with amide bond¡ªExtended cholesterol Ivan Černy, Miloš Bud¨§š¨ªnsky, Vladim¨ªr Pouzar, Pavel Drašar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3¦Â-hydroxy-35-(cyclohexyl-5'-propan-7'-one)-33-ethyl-34-methyl-bactereohopane C47H82O2 ÏàËÆ¶È:63.8% Chinese Chemical Letters 2011 22 81-84 A novel bacteriohopanoid from Celtis australis L. bark Ruchi Badoni, Deepak Kumar Semwal, Prabhakar P. Badoni, Sudhir Kumar Kothiyal, Usha Rawat Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . ¦Â-sitosteryl linoleate ÏàËÆ¶È:63.8% Natural Product Research and Development 2012 24 1738-1742 Chemical Constituents of Ceratocarpus arenarius L£® LIU Shan-shan, SUN Wen, YANG Hong-bing*, SUN Wan-fu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3-Oxo-5¦Â-cholan-24-oic acid (cholan-24-oic acidmethyl ester)-3-yl ester C49H79O5 ÏàËÆ¶È:63.2% Steroids 2003 68 1157-1161 Synthesis of ester-linked lithocholic acid dimers Lutfun Nahar, Alan B. Turner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3¦Á-Hydroxy-5¦Â-cholan-24-oic acid (cholan-24-oicacid methyl ester)-3-yl ester C49H81O5 ÏàËÆ¶È:63.2% Steroids 2003 68 1157-1161 Synthesis of ester-linked lithocholic acid dimers Lutfun Nahar, Alan B. Turner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . procrim a C46H80O3 ÏàËÆ¶È:63.0% Chemical & Pharmaceutical Bulletin 2002 50(3) 439-440 Two Novel Long-Chain Alkanoic Acid Esters of Lupeol from Alecrim-Propolis Satomi FURUKAWA,Naomichi TAKAGI,Tsuyoshi IKEDA,Masateru ONO,Alaa Mohamed NAFADY,Toshihiro NOHARA,Hiroyuki SUGIMOTO,Shima DOI,and Hideo YAMADA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . lanoscopariol C46H80O3 ÏàËÆ¶È:63.0% Journal of Natural Products 1996 59 181-184 New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia Surendra Kumar Sharma and Mohammad Ali Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ¦Â-sitosterol ¦Â-D-glucopyranoside tetraacetate ÏàËÆ¶È:63.0% Planta Medica 1993 59 369-372 A New Oleanolic Acid Derivative from Securinega tinctoria LuisM. Carvalho and J. Seita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . colebrin C C52H90O7 ÏàËÆ¶È:63.0% Fitoterapia 2000 71 641-648 New steroids from Clerodendrum colebrookianum Hui Yang, Jia Wang, Ai-Jun Hou, Yun-Pin Guo,Zhong-Wen Lin, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . sitosteryl-¦Â-D-glucopyranoside tetraacetate ÏàËÆ¶È:63.0% Phytochemistry 1991 30 3383-3387 Steroids and triterpenoids from Rosa laevigata Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 3,5-¶þôÇ»ù¶þÊ®ÍéËáÓðÉȶ¹´¼õ¥ C50H88O4 ÏàËÆ¶È:63.0% Chemical Journal of Chinese Universities 2003 24 436-441 Chemical Constituents from the Roots of Biondia Hemsleyana TAN Xing-Gen, ZHANG Xiao-Rong, PENG Shu-Lin, LIAO Xun, DING Li-Sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . mixture of compound 1a and compound 1b ÏàËÆ¶È:63.0% Phytochemistry 1989 28 1721-1724 Acylglucosyl sterols from Momordica charantia Amelia P. Guevara,Clara Y. Lim-Sylianco,Fabian M. Dayrit,Paul Finch Structure 13C NMR ̼Æ×Ä£Äâͼ |

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