Application of substituted benzoyl silybin in preparing medicament for treating virus hepatitis B
A technology of silybin ester and nitrobenzoyl, which is applied in the field of medicine, can solve the problems of less literature and no effective development, and achieve the effect of convenient source, convenient source of raw materials, and less pollution
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Embodiment 1
[0022] Example 1: The compound of formula (1) (±)-3-amino-5-nitrobenzoic acid [3-(4-hydroxy-3-methoxyphenyl)-6-(2,3-dihydro-3,5, Preparation of 7-trihydroxy-4-oxo-benzopyran-2)-2,3-dihydro-1,4-benzodioxane-2]-methyl ester
[0023] 1.1 Instruments and reagents:
[0024] UV spectrum was measured with Shimadzu UV-240 UV spectrophotometer; proton nuclear magnetic resonance spectrum 1 H-NMR was measured by INOVA superconducting nuclear magnetic resonance spectrometer (VARIAN INOVA-400MHz) (tetramethylsilyl ether TMS as internal standard); ESI-MS was measured by BrukerEsquire 3000+ mass spectrometer, and silica gel was used for column chromatography (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; the reagents used are all analytical pure, of which the boiling range of petroleum ether is 60-90℃; Thin-layer preparative chromatography (PTLC) uses Merck's aluminum foil silica gel plate; Sephadex L...
Embodiment 2
[0028] Example 2: The inhibitory effect of the compound of formula (1) on the replication of hepatitis B virus deoxyribonucleic acid (HBV DNA) secreted by HepG2.2.15 cells
[0029] 2.1 Cell culture:
[0030] 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.
[0031] 2.2 Determine the inhibitory effect of compound (1) on the growth of HepG2.2.15 cells by MTT method:
[0032] 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 well...
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