Application of physalin A in preparation of JAK2-STAT3 signal channel inhibitor and antitumor drug
A JAK2-STAT3, anti-tumor drug technology, applied in the field of anti-tumor drugs, can solve the problem of less research on anti-tumor mechanism, and achieve good anti-tumor activity
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Embodiment 1
[0074] Dry the persistent calyx (10.0kg) of the Physalis plant hanging golden lamp, and use 8 times the amount of 95% ethanol aqueous solution (80kg) to reflux extract 3 times, each time for 2 hours, and recover the obtained ethanol extract The extract can be obtained after there is no alcohol smell. The medicinal extract was dissolved in 3L of hot water, extracted 4 times with 1L of petroleum ether, 1L of dichloromethane and 1L of ethyl acetate successively to obtain the total sample of each extraction layer (30.5g of petroleum ether layer, Dichloromethane layer 160.0g, ethyl acetate layer 46.7g).
[0075] The dichloromethane layer (160.0g) was separated by silica gel column chromatography, and eluted sequentially with the dichloromethane / methanol elution system, and the elution gradients were 5, respectively 100:1, 50:1, 30:1, 20 :1 and 10:1 (dichloromethane to methanol volume ratio), Fr.1-55 fractions were obtained.
[0076] The Fr.2 fraction was separated by preparative ...
Embodiment 2
[0077] Example 2: Physalis A inhibits the JAK2 kinase 1007 / 1008 tyrosine (Tyr1007 / 1008) of human non-small cell lung cancer cell NCI-H292, and the phosphorylation level of JAK2 and its inhibitory effect are concentration- and time-dependent decline.
[0078] Such as figure 1 Shown: 5-15 μM Physalis A can inhibit the phosphorylation level of JAK2 in NCI-H292 cells in 4 hours, and 15 μM Physalis A can obviously inhibit the phosphorylation level of JAK2 in NCI-H292 cells in 2-4 hours. Phosphorylation level, its inhibition degree was time- and concentration-dependent, but physalicin A had no change on the expression of JAK2 total protein.
[0079] The experimental method is as follows:
[0080] NCI-H292 cells were cultured according to standard methods, and the medium used was RPMI1640 containing 10% FBS (GIBCO). When the cells grow to 70%-80%, add different concentrations of Physalis A to the culture medium, 37℃5%CO 2 Incubate in an incubator (Thermo), and after 4 hours of dr...
Embodiment 3
[0081] Example 3: The effect of physidin A on the phosphorylation level of Src kinase and the expression level of phosphatase SHP1 in human non-small cell lung cancer cell NCI-H292.
[0082] Such as figure 2 Shown: 15 μM Physalis A acts on NCI-H292 cells, and it has no significant effect on the phosphorylation level of the kinase Src upstream of STAT3 and the expression level of the phosphatase SHP1.
[0083] Experimental method is the same as embodiment 2.
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