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mlkyingгæ (³õÈëÎÄ̳)
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| 0.08, 12.36, 12.54, 13.27, 14.29, 19.84, 21.13, 21.72, 23.11, 23.72, 26.60, 29.81, 30.13, 32.39, 34.75, 37.57, 37.68, 45.26, 55.92, 55.61, 63.82, 65.95, 69.37, 70.22, 72.82, 73.74, 76.68 |
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mlkying: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-06 09:37:07
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mlkying: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-06 09:37:07
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1 . (20R,22R)-5¦Á-Cholestane-3¦Â,20,22-triol C27H48O3 ÏàËÆ¶È:65.3% Steroids 2008 73 1452-1464 Synthesis of ponasterone A derivatives with various steroid skeleton moieties and evaluation of their binding to the ecdysone receptor of Kc cells Hirokazu Arai, Bunta Watanabe, Yoshiaki Nakagawa, Hisashi Miyagawa Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . muriflasteroid A C28H46O4 ÏàËÆ¶È:64.2% Steroids 2013 78 108-114 3¦Â,5¦Á,6¦Â-Oxygenated sterols from the South China Sea gorgonian Muriceopsis flavida and their tumor cell growth inhibitory activity and apoptosis-inducing function Tao-Fang Liu, Xin Lu, Hua Tang, Min-Min Zhang, Pan Wang, Peng Sun, Zhi-Yong Liu, Zeng-Lei Wang, Ling Li, Yao-Cheng Rui, Tie-Jun Li, Wen Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 24-ethyl-4¦Á-methyl-cholestane-3,20-diol C30H45O2 ÏàËÆ¶È:63.3% Fitoterapia 2005 76 433-438 A new dihydroxysterol from the marine phytoplankton Diacronema sp. Am¨¦lia P. Rauter, Manuela M. Filipe, Carla Prata,João P. Noronha, Maria A.M. Sampayo,Jorge Justino,Jaime Bermejo Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (20S)-5¦Á-pregnane-3¦Â,20-diol 20-O-¦Â-D-glucopyranoside C27H46O7 ÏàËÆ¶È:62.9% Chinese Chemical Letters 2002 13 1189-1192 A New Pregnane Glycoside from Fermented Leaves of Agave americana Jian Ming JIN, Xi Kui LIU, Chong Ren YANG Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 6 C31H52O6 ÏàËÆ¶È:62.9% Tetrahedron 1998 54 179-186 New cytotoxic sterols from the soft coral Gersemia fruticosa Reet Koljak, Annika Lopp, Tõnis Pehk, K¨¹lliki Varvas, Aleksander-Mati M¨¹¨¹risepp, Ivar Järving, Nigulas Samel Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . stigmast-7-en-3¦Â-ol ÏàËÆ¶È:62.0% Acta Pharmaceutica Sinica 2000 Vol 35 29-31 STRUCTURE IDENTIFICATION OF VULGARSAPONIN A Tian Jing; Xiao Zhiyan; Chen Yayan; Zhao Yuying and Wang Zhuju Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . stigmast-7-en-3¦Â-ol ÏàËÆ¶È:62.0% Phytochemistry 1990 29 2351-2355 Sterol glucosides from Prunella vulgaris Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . stigmast-7-en-3¦Â-ol ÏàËÆ¶È:62.0% Chinese Traditional and Herbal Drugs 2009 40 1039-1042 ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿ »ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . stigmastane-3¦Â,6¦Á-diol ÏàËÆ¶È:62.0% Journal of Shenyang Pharmaceutical University 2009 26 357-360 Isolation and identification of chemical constituents from testa of Castanea mollissima Blume LU Chuan, WU Zhao-hua, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 22-dihydrochondrillasterol ÏàËÆ¶È:62.0% Journal of the Chemical Society, Perkin Transactions 1 1989 1969-1974 Biosynthesis of 24¦Â-ethylsterols in cultured cells of Trichosanthes kirilowii(cucurbitaceae) fed with [1,2-13C2]- and [2-13C2H3]-acetate: reinvestigation of the stereochemistry at C-25 Shujiro Seo, Atsuku Uomori, Yohko Yoshimura, Ken'ichi Takeda, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi and Ushio Sankawa Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (22R,23R)-Stigmasta-3¦Â,22,23-triol(6-deoxo-28-homoteasterone C29H52O3 ÏàËÆ¶È:62.0% Tetrahedron 2012 68 3685-3691 Synthesis of aromatic stigmastanes: application to the synthesis of aromatic analogs of brassinosteroids Sof¨ªa L. Acebedo, Fernando Alonso, Javier A. Ram¨ªrez, Lydia R. Galagovsky Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 5¦Á-stigmastane-3¦Â,6¦Á-diol C29H52O2 ÏàËÆ¶È:62.0% Natural Product Research and Development 2005 17 301-302 Chemical Constituents of Tripterygium wilfordii CHEN Yu; YANG Guang-zhong *; LI Yuan-chao Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5¦Á-sitgmasta-7-en-3¦Â-ol ÏàËÆ¶È:62.0% Journal of the Chinese Chemical Society 2000 47 1131-1136 The Low Polar Constituents from Bidens Pilosa L. var. minor (Blume) Sherff Ming-Huey Chang, Guei-Jane Wang,Yueh-Hsiung Kuo and Ching-Kuo Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . stigmast-7-en-3¦Â-ol ÏàËÆ¶È:62.0% Modern Chinese Medicine 2012 14 7-11 Separation and Identification of Chemical Constituents from Agriophyllum squarrosum( L. ) Moq. GONG Bang, ZHAN Kai-xuan, ZHOU Yu-hua, ZHANG Lan, HUI Ye-qian, LI Yu-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (22R,23R)-3,3-difluoro-22,23-dihydroxy-5¦Á-stigmastan-6-one C29H48F2O3 ÏàËÆ¶È:62.0% Steroids 2011 76 1016-1020 Synthesis and biological activity of ring-A difluorinated brassinosteroids Sof¨ªa L. Acebedo, Fernando Alonso, Lydia R. Galagovsky, Javier A. Ram¨ªrez Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 7(24S) ÏàËÆ¶È:62.0% Shoyakugaku Zasshi 1992 46 302-309 Chemical Components of a Commercial Crude Drug "Byakken" (Ampelopsis Radix) KATO TAKESHI, SUYAMA TETSUO, YAMANE FUJITOSHI, MORITA YUTAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ¡÷7-¶¹çÞÏ©´¼ ÏàËÆ¶È:62.0% Journal of Chinese Medicinal Materials 2011 34 553-555 Study on the Chemical Constituents of Codonopsis lanceolata WANG Wen-yong, ZHAO Shi-cheng, LIU Dong-xin Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . stigmastane-3¦Â,6¦Á-diol C29H52O2 ÏàËÆ¶È:62.0% Chinese Tladitional Patent Medicine 2008 30 419-423 »¨Éú¾¥Ò¶»¯Ñ§³É·ÖÑо¿ Áõ¾¢ËÉ, Íõ ¸ÕH, ¶ ³¬, Âé±ø¼Ì, Áõ¼ª¿ª Structure 13C NMR ̼Æ×Ä£Äâͼ |

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