Application of active ingredients of Trillium medicinal materials in preparation of liver-protecting or liver-protecting drugs
A technology of trillium and medicinal materials, which is applied in medical preparations containing active ingredients, organic active ingredients, drug combinations, etc.
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Embodiment 1
[0022]The present inventor through the intraperitoneal injection of 40% carbon tetrachloride olive oil solution while feeding and drinking 13 degrees of liquor-induced liver injury model, the research confirmed that Chinese Trillium or Pachyphylla medicinal materials pinanogenin-3-O-α -L-rhamnopyranosyl (1→2)-β-D-glucoside (i.e. saponin Ⅵ), pinanogenin-3-O-α-L-rhamnopyranosyl (1 →4)-[α-L-rhamnopyranosyl (1→2)]-β-D-glucoside and pinanogenin-3-O-α-L-rhamnopyranosyl (1 →4)-α-L-rhamnopyranosyl (1→4)-[α-L-rhamnopyranosyl (1→2)]-β-D-glucoside monomer compound has liver protection Or the pharmacological effect of protecting the liver, the above research has not been reported yet, we first found that the above three steroidal saponins in the medicinal materials of the genus Trillium or Pachyphylla have anti-inflammatory and anti-oxidative effects through the experimental research of whole animals. It has a protective effect on acute and chronic liver injury, and its active ingredient...
Embodiment 2
[0058] Pianogenin-3-O-α-L-rhamnopyranosyl (1→2)-β-D-glucoside (heavy Lou saponin Ⅵ), picanogenin-3-O-α-L-rhamnopyranosyl (1→4)-[α-L-rhamnopyranosyl (1→2)]-β- D-glucoside and pinanogenin-3-O-α-L-rhamnopyranosyl(1→4)-α-L-rhamnopyranosyl(1→4)-[α-L - Spectral data information and analysis of rhamnopyranosyl (1→2)]-β-D-glucoside.
[0059] 1. Pennogenin-3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucoside, that is, saponin VI (pennogenin-3-O-α-L- rhamnopyranosyl-(1→2)-β-D-glucopyranoside), colorless needles (methanol), molecular formula C 39 h 62 o 13 , ESI-MS[M+H] + Peak m / z: 739.4245. Both Liebermann-Burchard reaction and Molish reaction were positive for steroidal saponins. 1 H-NMR (DMSO-d 6 ,400MHz)δ:0.73(3H,s,CH 3 -18), 0.74 (3H, d, J = 6.0Hz, CH 3 -27), 0.78(3H,d,J=6.8Hz,CH 3 -21), 0.95 (3H,brs,CH 3 -19), 1.08 (3H, d, J=6.0Hz, Rha-CH 3 -6″), 5.34(1H,d,J=4.4Hz,H-6), 5.03(1H,d,J=0.8Hz,Rha-H-1″), 4.93(1H,d,J=6.0Hz ,Glc-H-1′); 13 C-NMR (DMSO-d 6 ,100MHz) δ: 36.9(C-1), 30.8(...
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