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xiling0505: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-11-19 22:39:26
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xiling0505: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-11-19 22:39:26
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²éѯ½á¹û£º¹²²éµ½369¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . cepagenin ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1987 23 700-706 STEROIDS OF THE SPIROSTAN AND FUROSTAN SERIES OF PLANTS OF THE Allium GENUS. XXIII. STRUCTURE OF CEPAGENIN AND OF ALLIOSPIROSIDES C AND D FROM Allium cepa S. D. Kravets, Yu. S. Vollerner, A. S. Shashkov, M. B. Gorovits, and N. K. Abubakir Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (25S*)-Cholest-5-ene-l(R*),3(R*),16(S*),22(S*),26-pentaol ÏàËÆ¶È:66.6% Phytochemistry 1996 41 907-917 Cholestane- and pregnane-type glycosides from the roots of Tribulus cistoides Hans Achenbach, Harald H¨¹bner, Melchior Reiter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . cepagenin ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1995 33 923-953 NMR spectroscopy of steroidal sapogenins and steroidal saponins: An update Pawan K. Agrawal, Dharam C. Jain and Ashish K. Pathak Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Cholest-5-ene-1(R*),3(R*),16(S*),22(S*)-tetraol ÏàËÆ¶È:62.9% Phytochemistry 1996 41 907-917 Cholestane- and pregnane-type glycosides from the roots of Tribulus cistoides Hans Achenbach, Harald H¨¹bner, Melchior Reiter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (22S)-3¦Â,16¦Â,22,25-tetrahydroxycholest-5-en-1¦Â-yl ¦Â-D-glucopyranoside aglycone C27H46O5 ÏàËÆ¶È:62.9% Chemical & Pharmaceutical Bulletin 2012 60(2) 275-279 New Cholestane Glycosides from the Leaves of Cordyline terminalis Akihito Yokosuka,Takeyuki Suzuki,and Yoshihiro Mimaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 14,15-dihydroajugapitin ÏàËÆ¶È:62.9% Phytochemistry 1990 29 2931-2933 Neo-clerodane diterpenoids from Ajuga chamaepitys Iva M. Boneva,Bozhana P. Mikhova,Peter Y. Malakov,Georgy Y. Papanov,Helmut Duddeck,Stefan L. Spassov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 22-methoxyfurostanol saponin C49H76O20 ÏàËÆ¶È:60.7% Molecules 2012 17 14002-14014 Novel Steroidal Components from the Underground Parts of Ruscus aculeatus L. Simona De Marino, Carmen Festa, Franco Zollo and Maria Iorizzi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . jasnudifloside F C27H42O13 ÏàËÆ¶È:59.2% Chemical & Pharmaceutical Bulletin 2002 50(3) 384-389 Nine New Secoiridoid Glucosides from Jasminum nudiflorum Yukiko TAKENAKA,Takao TANAHASHI, Hiromi TAGUCHI,Naotaka NAGAKURA, and Toyoyuki NISHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (20R)-5¦Á-cholestane-3¦Á,4¦Â,21-triol 3,21-disulfate C27H46O9S2Na2 ÏàËÆ¶È:59.2% Journal of Natural Products 2003 66 298-301 Hemolytic Steroid Disulfates from the Far Eastern Starfish Pteraster pulvillus Natalia V. Ivanchina, Alla A. Kicha, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, and Valentin A. Stonik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . certonardoside G C27H46O4 ÏàËÆ¶È:59.2% Journal of Natural Products 2003 66 384-391 Bioactive Sterols from the Starfish Certonardoa semiregularis Weihong Wang, Famei Li, Yujin Park, Jongki Hong, Chong-Ok Lee, Jae Yang Kong, Sook Shin, Kwang Sik Im, and Jee H. Jung Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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