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gaohongwei06: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-06-06 15:44:39
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gaohongwei06: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-06-06 15:44:39
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1 . compound III C30H48O4 ÏàËÆ¶È:100% Acta Pharmaceutica Sinica 1993 28 845-848 STUDIES ON THE TRITERPENES FROM BEMEUXIA THIBETICA DECNE MK Wang; FE Wu and YZ Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 2¦Á,3¦Á-dihydroxyurs-12-en-28-oic acid C30H48O4 ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2001 26 264-265 Lipid Chemical Constituents of Salvia sochifolia C. Y. Wu WU Zhijun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 2¦Á-hydroxyursolic acid C30H48O4 ÏàËÆ¶È:96.6% Acta Botanica Yunnanica 2008 30(1) 121-124 Triterpenoids from Saurauia napaulensis (Saurauiaceae) WANGQiong,JU Peng,WANG Yi-Fen,LUO Shi-De Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 216 ÏàËÆ¶È:96.6% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-epi-corosolic acid C30H48O4 ÏàËÆ¶È:96.6% Bioorganic & Medicinal Chemistry Letters 2007 17 5777-5782 Pentacyclic triterpenes. Part 5: Synthesis and SAR study of corosolic acid derivatives as inhibitors of glycogen phosphorylases Xiaoan Wen, Jun Xia, Keguang Cheng, Liying Zhang, Pu Zhang, Jun Liu, Luyong Zhang, Peizhou Ni, Hongbin Sun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 2¦Á,3¦Á-¶þôÇ»ùÐܹûËá ÏàËÆ¶È:96.6% Chinese Traditional and Herbal Drugs 2010 41 544-546 ºÚ¹ûÏÙÀß»¨é±¹ûʵµÄ»¯Ñ§³É·Ö ÓÚÃ÷;Àîϳ;ÕÅÀö;ÕÔÓàÇì Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 2¦Á,3¦Á-dihydroxyursolic acid ÏàËÆ¶È:96.6% Natural Product Research and Development 2003 15 490-493 STUDIES ON THE CHEMICAL CONSTITUENTS FROM RABDOSIA JAPONICA(BURM. F.) HARA VAR. GLAUCOCALYX(MAXIM.) HARA YANG Xiu-wei; ZHAO Jing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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