Eudesmane type sesquiterpenes acid and application thereof
A technology of sesquiterpene and eucalyptane type, applied in eucalyptane type sesquiterpene acid and its application field, can solve the problems of reducing hepatitis B surface antigen, and there is no anti-hepatitis B virus drug for hepatitis B virus infectious disease
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Embodiment 1
[0020] The preparation method of embodiment 1 eucalyptane type sesquiterpene acid
[0021] The present invention prepares the target compound ( A)-Pectic acid, the spectral data after purification are consistent with the reported values in the literature,
[0022] The spectral data of the prepared compound is: mass spectrum EIMS: m / z 252[M] + (5), 234, 219, 206, 191, 149, 81; 1 H-NMR (deuterated chloroform, 400MHz) δ6.13 (1H, brs), 5.63 (1H, brs), 2.46 (1H, dddd, J=12.0, 12.0, 3.0, 3.0Hz), 2.04 (1H, ddd, J=13.5, 12.0, 3.0 Hz), 1.45-1.55 (5H, m), 1.20-1.35 (2H, m), 1.05 (1H, brs), 0.92 (3H, s).
[0023] The structure of compound (A):
[0024]
Embodiment 2
[0025] Example 2: Inhibitory effect of compound (A) on hepatitis B surface antigen (HBsAg) secreted by HepG2.2.15 cells.
[0026] 1) Cell culture:
[0027] HepG2.2.15 cells were cultured in DMEM medium containing 10% inactivated fetal bovine serum, 100 U / ml penicillin and 100 μg / ml streptomycin, 100 μg / ml G418 at 37°C, 5% CO 2 , cultured in an incubator with 100% relative humidity.
[0028] 2) The inhibitory effect of the compound of formula (A) on the growth of HepG2.2.15 cells was measured by MTT method:
[0029]Take the HepG2.2.15 cells in the logarithmic growth phase, and dilute the cells to 1×10 with medium 5 / ml, seeded in 96-well cell culture plate, 100 μl per well, at 37°C, 5% CO 2 After cultivating in an incubator with 100% relative humidity for 24 hours, add compound (A) diluted with medium, the concentrations are 1000 μg / ml, 200 μg / ml, 40 μg / ml and 8 μg / ml, 200 μl per hole, each concentration Set up three replicate wells, placed at 37°C, 5% CO 2 , cultivated in...
Embodiment 3
[0036] Embodiment 3: Compound (A) inhibits the replication of hepatitis B virus deoxyribonucleic acid (HBV-DNA) secreted by HepG2.2.15 cells.
[0037] 1) Cell culture: the method is the same as in Example 1.
[0038] 2) Determination of the inhibitory effect of compound (A) on the growth of HepG2.2.15 cells by MTT method: the method is the same as in Example 1.
[0039] 3) Determining the inhibitory effect of compound (A) on the replication of hepatitis B virus deoxyribonucleic acid (HBV-DNA).
[0040] Take the HepG2.2.15 cells in the logarithmic growth phase, and dilute the cells to 1×10 with medium 5 / ml, seeded in 96-well cell culture plate, 100 μl per well, at 37°C, 5% CO 2 After cultivating in an incubator with 100% relative humidity for 24 hours, add compound (A) diluted with culture medium, the concentrations are 100 μg / ml, 20 μg / ml and 40 μg / ml respectively, 200 μl per hole, and each concentration is set in triplicate. Wells, placed at 37°C, 5% CO 2 , cultivated in...
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