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JGX-H-47 CÆ×Êý¾Ý£º12.04,12.17,12.23,12.43,18.98,19.19,19.25,19.58,20.00,21.27,21.42,23.26,24.49,24.55,25.59,26.31,28.43,29.10,29.36,31.78,32.09,34.14,36.34,36.68,37.46,39.88,39.98,40.68,42.39,42.44,42.50,46.01,50.33,50.36,51.43,56.15,56.27,56.96,57.06,71.88,121.83,129.46,138.49,140.96 |
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Ò©»¯Àí¹¤ÄÐ: ½ð±Ò+10, ¡ïÓаïÖú 2015-05-30 14:35:44
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1 . stigmasteryl-3¦Â-arachidate C49H86O2 ÏàËÆ¶È:81.8% Asian Journal of Chemistry 2014 26 3018-3020 Stigmasteryl Arachidate Constituent from the Straw of Oryza sativa ILL-MIN CHUNG, JAE-YEON YOON, SEUNG-HYUN KIM and ATEEQUE AHMAD Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound A ÏàËÆ¶È:76.0% Yakugaku Zasshi 1983 103 43-48 The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A) EMI OKUYAMA, MIKIO YAMAZAKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . mixture of ¦Â-sitosterol-3-O-¦Â-D-glucoside and stigmasterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:75% The Chinese Pharmaceutical Journal 2003 55 109-119 Antiproliferative Constituents from Gynura divaricata subsp. formosana Sheng-Chih Chen*, Li-Ling Hong, Chung-Yang Chang, Chun-Jen Chen, Mei-Hua Hsu, Yuan-Chao Huang, Tai-Hung Huang and Sheng-Chu Kuo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-sitosterol ÏàËÆ¶È:72.7% Chemistry of Natural Compounds 1999 35 646-649 13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . crotasteroiridocin C39H64O3 ÏàËÆ¶È:72.7% Zeitschrift f¨¹r Naturforschung B 2006 61 629-635 Behavior of 1,3-Di(tert-butyl)-2,4-bis(tetramethylpiperidino)-1,3,2,4-di-phospha-diboretane towards Boron Halides and Adduct Formation of a Bicyclo[1.1.0]diphosphadiboretane with Tris(pentafluorophenyl)borane K. Knabel, H. Nöth, and R. T. Paine Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . aglycone-II ÏàËÆ¶È:72.7% Yakugaku Zasshi 1983 103 43-48 The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A) EMI OKUYAMA, MIKIO YAMAZAKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . artemisterol B C44H72O4 ÏàËÆ¶È:70.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol ¦Â-D-glucopyranoside tetraacetate ÏàËÆ¶È:70.4% Planta Medica 1993 59 369-372 A New Oleanolic Acid Derivative from Securinega tinctoria LuisM. Carvalho and J. Seita Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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