Application of E-ring demethoxy-silibinin for preparing medicament for treating viral hepatitis B
A technology for viral hepatitis and milk thistle, applied in the field of medicine, can solve the problems that new uses have not been effectively developed, and achieve the effects of convenient source of raw materials, large-scale production of energy saving and emission reduction, and convenient synthesis
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Embodiment 1
[0029] Example 1: The compound of formula (1) (±)-2-[2,3-dihydro-3-(4-hydroxyphenyl)-2-hydroxymethyl-1,4-benzodioxane-6-]- Preparation of 2,3-dihydro-3,5,7-trihydroxy-4H-1-benzopyran-4-one
[0030] 1.1 Instruments and reagents:
[0031] UV spectrum was measured with Shimadzu UV-240 UV spectrophotometer; proton nuclear magnetic resonance spectrum 1 H-NMR is measured by INOVA superconducting nuclear magnetic resonance spectrometer (VARIAN INOVA-400MHz) (tetramethylsilyl ether TMS is the internal standard); ESI-MS is measured by BrukerEsquire 3000+ mass spectrometer, column chromatography uses silica gel (100-200, 200-300 and 300-400 mesh) and thin layer chromatography silica gel GF254 (10-40 mesh) are produced by Qingdao Ocean Chemical Plant; all reagents used are analytical pure, thin layer preparative chromatography (PTLC) ) Use Merck's aluminum foil silica gel plate; Sephadex LH-20 for column chromatography uses the product of Amersham Pharmacia Biotech AB in Sweden; reverse-pha...
Embodiment 2
[0038] Example 2: Inhibitory effect of compound (1) on hepatitis B surface antigen (HBsAg) secreted by HepG2.2.15 cells
[0039] 2.1 Cell culture:
[0040] HepG2.2.15 cells were cultured in DMEM medium containing 10% inactivated fetal bovine serum, 100U / ml penicillin and 100U / ml streptomycin, 100μg / ml G418, and placed at 37°C, 5% CO 2 , Cultivate in an incubator with 100% relative humidity.
[0041] 2.2 Determine the inhibitory effect of the compound of formula (1) on the growth of HepG2.2.15 cells by MTT method:
[0042] Take HepG2.2.15 cells in logarithmic growth phase and dilute the cells to 1×10 with medium 5 Pcs / ml, seeded on 96-well cell culture plate, 100 microliters per well, at 37℃, 5% CO 2 After culturing in a 100% relative humidity incubator for 24 hours, add the compound (1) diluted with the medium at the concentration of 1000 μg / ml, 200 μg / ml, 40 μg / ml and 8 μg / ml, 200 per well Microliters, each concentration has three replicate wells, placed at 37℃, 5% CO 2 Cultivate in...
Embodiment 3
[0051] Example 3: Inhibitory effect of compound (1) on hepatitis B e antigen (HBeAg) secreted by HepG2.2.15 cells
[0052] 3.1 Cell culture: The method is the same as in Example 2.
[0053] 3.2 The MTT method was used to determine the inhibitory effect of the compound of formula (1) on the growth of HepG2.2.15 cells: the method was the same as in Example 2.
[0054] 3.3 Determine the inhibitory effect of the compound on hepatitis B e antigen (HBeAg): Take HepG2.2.15 cells in the logarithmic growth phase and dilute the cells to 1×10 with culture medium 5 / Ml, seeded in 96-well cell culture plate, 100ml per well, at 37℃, 5% CO 2 After culturing in a 100% relative humidity incubator for 24 hours, add samples diluted with culture medium at concentrations of 20 micrograms / ml, 4 micrograms / ml and 0.8 micrograms / ml, 200 microliters per well, and three for each concentration. Multiple holes, placed at 37℃, 5% CO 2 , Cultivate in a 100% relative humidity incubator, change the medium containi...
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