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²éѯ½á¹û£º¹²²éµ½2284¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . pulsatilloside C C48H78O18 ÏàËÆ¶È:81.6% Journal of Natural Products 1998 61 658-659 Pulsatilloside C from the Roots of Pulsatilla chinensis Wencai Ye, Aimin He, Shouxun Zhao, and Chun-Tao Che Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . HN saponin H C48H78O18 ÏàËÆ¶È:81.6% China Journal of Chinese Materia Medica 2008 33 1377-1382 Studies Chemical Constituents of Clematis puberula Hook. f. & Thoms. var. Ganpinian (Lvl & Van.)W. T. Wang SUN Feng, HE Qing, XIAO Peigen, CHENG Yiyu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . HN saponin H C48H79O18 ÏàËÆ¶È:81.6% Chinese Pharmaceutical Journal 2008 43 1377-1382 Studies on Chemical Constituents of Clematis puberula Hook.f.& Thoms.var.ganpiniana(L vl.& Van.) W.T.Wang SUN Feng, HE Qing, XIAO Pei-gen, CHENG Yi-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . calendasaponin A C54H86O24 ÏàËÆ¶È:79.6% Chemical & Pharmaceutical Bulletin 2001 49(7) 863-870 Medicinal Flowers. III.1) Marigold. (1): Hypoglycemic, Gastric Emptying Inhibitory, and Gastroprotective Principles and New Oleanane-Type Triterpene Oligoglycosides, Calendasaponins A, B, C, and D, from Egyptian Calendula officinalis Masayuki YOSHIKAWA, Toshiyuki MURAKAMI, Akinobu KISHI, Tadashi KAGEURA, and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Glycoside G C48H78O18 ÏàËÆ¶È:79.5% Chemical Research in Chinese Universities 1994 10 285-290 Isolation and Structure Elucidation of New Glycosides from the Leaves of Oplopanax Elatus Nakai(II) WANG Guang-shu,ZHAO Chun-fang and XU Jing-da Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . oplopanaxoside E C48H78O18 ÏàËÆ¶È:79.5% Natural Medicines 1995 49 462-467 Three New Lupane Type Glycosyl Esters from Oplopanax japonicus Leaves HIRAI YASUAKI,MURAYAMA TETSUYA, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 1b ÏàËÆ¶È:78% Chemistry of Natural Compounds 2005 41 436-441 TRITERPENE GLYCOSIDES FROM Cussonia paniculata.II. ACETYLATED GLYCOSIDES FROM LEAVES V. I. Grishkovets, I. I. Dovgii, V. V. Kachala,and A. S. Shashkov Structure 13C NMR ̼Æ×Ä£Äâͼ |
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