Monoiodobenzoic acid compound and application thereof in resisting ADV7 virus
A technology of iodobenzoic acid and iodobenzoic acid, which is applied in the direction of antiviral agents, medical preparations containing active ingredients, and pharmaceutical formulas, can solve the problems of unreported inhibitory activity, and achieve easy large-scale production promotion and synthesis Simple process, economical and fast effect
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Embodiment 1
[0030] [Example 1] Research experiment on anti-ADV7 activity of monoiodobenzoic acid compounds L1-L3
[0031] In the present embodiment, the anti-ADV7 activity research experiment was carried out to the above-mentioned compound, and the experimental situation is as follows:
[0032] 1. Test content:
[0033] Anti-ADV7 activity analysis of compounds: In the present invention, the anti-ADV7 activity of monoiodobenzoic acid will be evaluated by combining cytopathic effect analysis and MTT assay cell survival rate detection method.
[0034] 2. Test method:
[0035] 2.1.1 Toxicity of compounds to host Hela cells
[0036] Hela cells were plated in 96-well plates at 37°C, 5% CO 2 After the monolayer was grown in the incubator, the cell culture solution was discarded, and the cell maintenance solution containing different concentrations of the test compound was added to continue the culture. After 48 hours, the cytotoxicity was visually observed under the microscope and recorded re...
Embodiment 2
[0048] [Example 2] Inhibition test of monoiodobenzoic acid compounds L1, L3 on ADV7 progeny virus output
[0049] In this embodiment, monoiodobenzoic acid has been carried out in-depth research on the anti-ADV7 activity, and the inhibitory effect test of compounds L1 and L3 on the production of ADV7 progeny virus has been carried out. The test conditions are as follows:
[0050] 1. Test content
[0051] After ADV7 infected Hela cells, the inhibitory effect of compounds L1 and L3 on the production of ADV7 progeny virus was detected.
[0052] 2. Test method
[0053] Hela cells in the logarithmic growth phase were plated in 24-well plates, and 100TCID after the monolayer was overgrown 50 ADV7 infected cells, incubated at 37°C for 1.5h, removed the virus solution, washed three times with PBS, and added cell maintenance solution containing 25 μg / mL L1 and 50 μg / mL L3. After 48 hours, the cells and supernatant were collected and lysed by freezing and thawing three times at -20°C ...
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