Novel steroid saponin compound and application thereof
A technology of steroidal saponins and compounds, applied in the field of medicine, can solve the problems of incomplete research on the chemical components of Solanum solanum fruit, the chemical structure and anti-inflammatory and anti-tumor activities have not been reported, and achieve good anti-inflammatory activity in vitro, Effect of clear chemical structure
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Embodiment 1
[0031] The extraction of embodiment 1 steroidal saponins
[0032] Take 6 kg of dried Solanum solanum fruit, extract twice with cyclohexane under reflux, and discard the cyclohexane extract. The medicinal material after degreasing treatment is heated and refluxed with 10 times the amount of 70% methanol and extracted three times for 2 hours each time, and the combined extracts are concentrated under reduced pressure to obtain the extract. Suspend the extract in water, pass through a D101 macroporous resin column (1300×100mm), and elute with water, 10% methanol, 30% methanol, 50% methanol, 70% methanol and 100% methanol, among which 50% methanol Compound 1-9 was isolated by repeated silica gel column chromatography, reverse phase MPLC column chromatography, Sephadex LH-20 column chromatography and semi-preparative reverse phase HPLC column chromatography.
Embodiment 2
[0033] Identification of Example 2 Compound 1
[0034] By means of physical and chemical constants and spectroscopy (HRESIMS, 1 H-NMR, 13 C-NMR, HSQC, HMBC and 1 H- 1 H COZY spectrum) to identify compound 1, the results are as follows:
[0035] Compound 1 is a white amorphous powder, The reaction to Anisaldehyde (A reagent) showed yellow color, and Ehrlish (E reagent) showed no color, and acid hydrolysis detected D-glucose and D-galactose, suggesting that the compound was a spirosteroid saponin compound. HRESIMS (positive) gives the quasi-molecular ion peak [M+NH 4 ] + m / z 1128.5492 (calcd.forC 51 h 86 NO 26 1128.5438), suggesting that its molecular weight is 1110, combined with 1 H-NMR and 13 C-NMR (DEPT) can determine its molecular formula as C 51 h 82 o 26 .
[0036] exist 1 In the H-NMR spectrum, the high-field region gives four characteristic methyl signals on steroidal saponins, two of which are single-peaked and the other two are double-peaked, respect...
Embodiment 3
[0042] Identification of Example 3 Compound 2
[0043] By means of physical and chemical constants and spectroscopy (HRESIMS, 1 H-NMR, 13 C-NMR, HSQC, HMBC and 1 H- 1 H COZY spectrum) to identify compound 2, the results are as follows:
[0044] Compound 2 is a white amorphous powder, The reaction to Anisaldehyde (A reagent) showed yellow color, but to Ehrlish (E reagent) showed no color, and acid hydrolysis detected D-glucose and D-galactose, suggesting that the compound was a spirosteroid saponin compound. HRESIMS (positive) gives the quasi-molecular ion peak [M+NH 4 ] + m / z 1128.5497 (calcd.forC 51 h 86 NO 26 1128.5438), suggesting that its molecular weight is 1110, combined with 1 H-NMR and 13 C-NMR (DEPT) can determine its molecular formula as C 51 h 82 o 26 .
[0045] exist 1 In the H-NMR spectrum, the high-field region gives four characteristic methyl signals on steroidal saponins, two of which are single peaks and the other two are double peaks, respec...
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