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²éѯ½á¹û£º¹²²éµ½267¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol and stigmasterol ÏàËÆ¶È:82.7% China Journal of Chinese Materia Medica 2001 26 692-694 Chemical Constituents of loxocalyx urticifolius Hemsl ZHANG Xiaorong, WANG Ming'an, ZHANG Yong, WANG Mingkui, IDNG Lisheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . sitosterol ÏàËÆ¶È:79.3% Chemical Communications 1986 1139-1140 Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from [2-13C, 2-2H3]Acetate Shujiro Seo, * Ushio Sankawa, Haruo Seto, Atsuko Uomori, Yohko Yoshimura, Yutaka Ebizuka, Hiroshi Noguchi, and Ken'ichi Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . N-palmitoyl aminobacteriohopanetriol ÏàËÆ¶È:77.7% Tetrahedron Letters 1999 40 1681-1684 Novel bacterial triterpenoids of the hopane series from Nitrosomonas europaea and their significance for the formation of the C35 bacteriohopane skeleton Myriam Seemann, Philippe Bisseret, Jean-Philippe Tritz, Alan B. Hooper, Michel Rohmer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . bisconicasterone ÏàËÆ¶È:77.7% Chemistry Letters 1994 23 419-420 Structure and Absolute Stereochemistry of Bisconicasterone from the Marine Sponge Theonella swinhoei Yoshinobu Inouye, Yumi Sugo, Takenori Kusumi and Nobuhiro Fusetani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 16a+17a ÏàËÆ¶È:77.7% Steroids 2012 77 780-790 A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: Application to the preparation of early brassinolide biosynthetic precursors Alaksiej L. Hurski, Vladimir N. Zhabinskii, Vladimir A. Khripach Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (24R)-[26,26-2H2]-6-(1,3-Dioxolan-2-yl)-24-methyl-3¦Á,5-cyclo-5¦Á-cholestan-22-ol ÏàËÆ¶È:77.7% Steroids 2012 77 780-790 A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: Application to the preparation of early brassinolide biosynthetic precursors Alaksiej L. Hurski, Vladimir N. Zhabinskii, Vladimir A. Khripach Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5¦Á-stigmast-9(11)-en-3¦Â-ol-tetraco santrienoic acid ester ÏàËÆ¶È:75.9% China Journal of Chinese Materia Medica 1996 21 666-667 Studies on Chemical Components of Cynomorium songaricum Rupr. Xu Xiuzhi, Zhang Chengzhong and Li Chong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . daucosterol+stigmasterol-3-O-glucopyranoside ÏàËÆ¶È:75.9% Chinese Traditional and Herbal Drugs 2004 35 608-611 Studies on chemical constituents of Indigofera carlesii SU Yan-fang; ZHANG Xin-xin; YANG Jing; GUO Zeng-jun; L¨¹ Ju-xian; GUO De-an Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-Oxo-5¦Â-cholan-24-oic acid (cholan-24-oic acidmethyl ester)-3-yl ester C49H79O5 ÏàËÆ¶È:74.0% Steroids 2003 68 1157-1161 Synthesis of ester-linked lithocholic acid dimers Lutfun Nahar, Alan B. Turner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 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:74.0% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Manadosterol A C54H83NaO21S5 ÏàËÆ¶È:74.0% Journal of Natural Products 2012 75 1495-1499 Manadosterols A and B, Sulfonated Sterol Dimers Inhibiting the Ubc13¨CUev1A Interaction, Isolated from the Marine Sponge Lissodendryx fibrosa Shuntaro Ushiyama, Hideharu Umaoka, Hikaru Kato, Yoshiaki Suwa, Hiroshi Morioka, Henki Rotinsulu, Fitje Losung, Remy E. P. Mangindaan, Nicole J. de Voogd, Hideyoshi Yokosawa, and Sachiko Tsukamoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (+/-)-7¦Á,12¦Á-Dihydroxy-3¦Á-(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oic acid C57H92O9 ÏàËÆ¶È:73.2% Steroids 2013 78 435-453 New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (20R,25R)-5¦Á- spirostane-3¦Â,6¦Á,20-triol C27H44O5 ÏàËÆ¶È:72.2% Chemical & Pharmaceutical Bulletin 2007 55(1) 145-149 Steroidal Glycosides from Agave utahensis Akihito YOKOSUKA and Yoshihiro MIMAKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 24(R/S),25-epoxy-6¦Â-hydroxycholest-4-en-3 C27H4203 ÏàËÆ¶È:72.2% Journal of Natural Products 1996 59 23-26 Cytotoxic Oxygenated Desmosterols of the Red Alga Galaxaura marginata Jyh-Horng Sheu, Shiang-Yuh Huang, and Chang-Yih Duh |

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