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13C NMR (dmso) 65.17,70.32,79.36,83.68,85.92,86.94,103.44,108.70,110.51,112.73,122.92,124.58,130.39,140.28,142.55,156.37,165.23,166.02,169.29,170.60,186.60
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1 .     chrysophanol 8-O-¦Â-D-glucopyranoside
C21H20O9     ÏàËÆ¶È:52.3%
Chinese Traditional and Herbal Drugs          2009          40          1352-1355
Chemical components of Rumex gmelini (¢ô)
WANG Zhen-yue; CHEN Jin-ming; WANG Qian-bo; KANG Yi-hua; LIU Ying-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (2R)-2-(acetyloxy)-4-({[(2Z,3E)-2-(1,2-dihydro-2-oxo-3H-indol-3-ylidene)-1,2-dihydro-3H-indol-3-ylidene]amino}oxy)-N,N,N-trimethyl-4-oxobutan-1-aminium chloride
C25H27ClN4O5     ÏàËÆ¶È:52.1%
Chemistry & Biodiversity          2012          9          2175-2185
Water-Soluble Cationic Derivatives of Indirubin, the Active Anticancer Component from Indigo naturalis
Werner Ginzinger, Alexander Egger, Gerhard M¨¹hlgassner, Vladimir B. Arion, Michael A. Jakupec, Markus Galanski, Walter Berger and Bernhard K. Keppler
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     11dM-PN II
C24H16O11     ÏàËÆ¶È:50%
The Journal of Antibiotics          1993          46          420-429
BIOSYNTHESIS OF THE PRADIMICIN FAMILY OF ANTIBIOTICS II. FERMENTATION, ISOLATION AND STRUCTURE DETERMINATION OF METABOLITES ASSOCIATED WITH THE PRADIMICINS BIOSYNTHESIS
TAKASHI TSUNO, HARUAKI YAMAMOTO, YUKIO NARITA, KIYOSHI SUZUKI, TOSHIFUMI HASEGAWA, SHIZUKO KAKINUMA, KYOICHIRO SAITOH, TAMOTSU FURUMAI, TOSHIKAZU OKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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