Medical use of 2 alpha, 3 beta-dihydroxy-5, 11(13)- diallyl eudesmane-12 acid for inhibiting hepatitis B virus
A technology of diene eucalyptane and dihydroxy, which is applied in the field of natural product eucalyptane-type sesquiterpene acids, can solve the problems of reducing hepatitis B surface antigen, and there is no anti-hepatitis B virus drug for hepatitis B virus infectious diseases.
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[0019] The preparation method of the eucalyptane-type sesquiterpene acid shown in this formula (1) can be referred to the article published by researchers such as the inventor (Li Shunlin, Ding Jingkai, Yunnan Plant Research, 1996, 18 (3), 349; Zheng Qunxiong , Zhang Qijun, Zhao Yu, etc., Zhejiang University Journal (Medical Edition), 2002, 31(6): 406; (Zheng Qunxiong, Zhao Yu, etc., J Nat Prod, 2003, 66(8): 1078. According to the literature described Method prepares formula (1) compound, its spectral data of the formula (1) compound that purifies obtains and 2α in the above-mentioned literature, 3β-dihydroxy pterodontic acid, namely 2α, the reported value of 3β-dihydroxy malidontic acid is consistent. Here According to its scientific name, the compound of formula (1) is 2α, 3β-dihydroxy-5, 11(13)-diene eucalyptus-12-acid, and its English name is: 2α, 3β-dihydroxy-5, 11(13 )-dien-eudesman-12-oic acid.
[0020] Compound of formula (1): colorless block crystal (acetone), meltin...
Embodiment 1
[0022] Example 1 Inhibitory effect of formula (1) compound on the hepatitis B surface antigen (HBsAg) secreted by HepG2.2.15 cells
[0023] 1) Cell culture:
[0024] 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.
[0025] 2) The inhibitory effect of the compound of formula (1) on HepG2.2.15 cell growth was measured by MTT method:
[0026] 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 the compound of formula (1) diluted with medium, the concentration is respectively 1000 μg / ml, 200 μg / ml, 40 μg / ml and 8 μg / ml, 200 μl in each well, each Concentration Set up three replicate wells, placed...
Embodiment 2
[0034] Example 2 : formula (1) compound is to HepG2.2.15 cell secreted hepatitis B virus deoxyribonucleic acid (HBV-DNA) replication inhibitory effect
[0035] 1) Cell culture:
[0036] Method is with embodiment 1.
[0037] 2) The inhibitory effect of the compound of formula (1) on HepG2.2.15 cell growth was measured by MTT method:
[0038] Method is with embodiment 1.
[0039] 3) Determination of the inhibitory effect of the compound of formula (1) 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 the compound of formula (1) diluted with medium, the concentration is respectively 100 μg / ml, 20 μg / ml and 40 μg / ml, 200 μl per well, and three concentrations are set for each Duplicate wel...
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