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3Â¥2010-10-08 18:52:52
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White powder Compound 1 , mp246 ~ 248 ¡æ, Libermann-Burchard-positive, Ehrlish reaction was red, presumably furostanol saponins, acid hydrolysis detected D-glucose and D-galactose, D-amygdalin enzymatic detection of glucose, D-galactose showed that even on the aglycone. ESI-MS gives the molecular ion peak 920.

1H-NMR (C5D5N, ¦Ä, ppm) in, 5.28 (1H, d, J = 7Hz), 4.91 (1H, d, J = 8Hz), 4.80 (1H, d, J = 8Hz), for the sugar on the side matrix sub-signals, the coupling constant values that were ¦Â-side configuration of carbon, 1.32 (3H, d), 1.03 (3H, d), 0.98 (3H, s), 0.88 (3H, s) for the four methyl H signal.

13C-NMR (C5D5N, ¦Ä, ppm) in, ¦Ä105.7, 104.8,102.2 end groups for the sugar carbon signals, 110.4 for the season, carbon, high-field region of the carbon on the removal of sugar, 4 CH3, 12 ¸ö CH2, 7 CH, 3 quarters of carbon, with 27 of its aglycone carbon, according to the chemical shift and chemical types of carbon, suggesting that aglycone structure of 25 (S) -22 - hydroxy-5¦Â furostanol-3¦Â, 26 - II alcohol. The foregoing analysis, aglycone 3 connections sugar ¦Â-D-glucopyranosyl (1 ¡ú 2)-¦Â-D-pyran-galactose, 26 connecting ¦Â-D-glucopyranose.

Light yellow needle crystal of compound 2, mp260 ~ 261 ¡æ. FeCl3 reagent was dirty and green, on the HCl-Mg reaction was orange red. ESI-MS shows ions m/z445 [M + Na] +, 423 [M +1] +, showed that the molecular weight of compounds 6, 422.
1H-NMR (DMSO-d6, ¦Ä) in, 4.61 (1H, d, J = 9.8Hz) glucose as a substrate sub-terminal, and for the ¦Â-glucoside bond form. Another 6.39 (1H, s), 6.88 (1H, s) and 7.40 (1H, s) 3 ¸ö aromatic proton signals.


13C-NMR and DEPT (DMSO-d6, ¦Ä), in the low field region, 179.1 for the carbonyl signal, 163.6,161.4,156.3,153.8,150.8,143.6,111.8,108.1,107.5,102.6,101.3,93.4 12 a signal suggestive of two benzene rings exist. In the high field region have a six-carbon sugar signal, namely: 81.5,78.8,73.1,70.5,70.2,61.4.
2Â¥2010-10-07 20:04:18
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happykeren2008(½ð±Ò+1000, ·­ÒëEPI+1):лл 2010-10-10 20:46:36
Compound 1   
Compound 1, white powered, melting point 246~248¡æ, which exhibits positive in Libermann-Burchard reaction and red in Ehrlish reaction was supposed to be furostanol saponins. Detection of D-glucose and D-galactose with acid hydrolysis and D-glucose with emulsin enzymolysis indicates that D-galactose was connected to the aglycone. ESI-MS manifests molecularion peak at 920.

For 1H-NMR test (C5D5N, ¦Ä, ppm), anomeric proton signal of carbohydrate are 5.28(1H, d, J=7Hz), 4.91(1H, d, J=8Hz) and 4.80(1H, d, J=8Hz), while coupling constant values of compound 1 indicates the ¦Â-configuration of all anomeric carbons. 1.32(3H, d), 1.03(3H, d), 0.98(3H, s) and 0.88(3H, s) are four methyl hydrogen signals.

For 13C-NMR test (C5D5N, ¦Ä, ppm), ¦Ä105.7, 104.8, 102.2 and 110.4 are anomeric carbons signals of carbohydrate and 110.4 represents C-1. Excluding carbon from carbohydrate in upfield region, there are four CH3£¬twelve CH2£¬seven CH and three quaternary carbons. Aglycone of compound 1 contains twenty-seven carbons.  
In accordance with chemical shift and type of carbons in the aglycone, it is suspected that the structure of aglycone is 25(s)-22-hydroxy-5¦Â furostanol-3¦Â, 26-glycol. Based upon the analysis listed above, carbohydrate connected to C3 of aglycone is ¦Â-D-glucopyranosyl(1¡ú2)-¦Â-D-galactopyranose and C26 of aglycone is ¦Â-D-glucopyranose.


Compound 2   
Compound 2, which is buff acicular crystal, exhibits dirty green in reaction with FeCl3 and almon pink in HCL-Mg reaction. ESI-MS manifests molecularion peak at m/z445 [M+Na]+, 423[M+1]+ indicates molecular mass of compound 6 is 422.

For 1H-NMR test (DMSO-d6, ¦Ä), 4.61(1H, d, J=9.8Hz) represents one glucose anomeric proton which exists as ¦Â-glucoside bond. In addition, 6.39(1H, s), 6.88(1H, s) and 7.40(1H, s) are three aromatic protons.

For 13C-NMR and DEPT (DMSO-d6, ¦Ä) test, 179.1 is carbonyl signal in downfield region and twelve signals of 163.6, 161.4, 156.3, 153.8, 150.8, 143.6, 111.8, 108.1, 107.5, 102.6, 101.3, and 93.4 indicate the compound includes two benzene rings. 81.5, 78.8, 73.1, 70.5, 70.2 and 61.4 represents a hexose signal in upfield region.
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