Carboxamide compound and application thereof
A compound and carboxylamine technology, applied in the field of drug preparation for preventing and treating animal viral diseases, can solve problems such as failure to effectively control the growth or proliferation of vesicular stomatitis virus, and achieve the advantages of overcoming high cost, preventing proliferation and low biological toxicity. Effect
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Embodiment 1
[0039] Baby hamster kidney cells (BHK21) were cultured in DMEM medium containing 10% fetal calf serum at 37°C and 5% CO 2 When cultured to 90% confluence under ambient conditions, the compound 2-imino-2H-chromene-3-carboxamide was added to the 6-well plate at a dose of 100 μl / well, and the effect of the compound on the growth of BHK21 cells was observed after 24 hours. Figure 4 is the effect of 2-imino-2H-chromene-3-carboxamide on the growth of BHK21 cells, wherein Figure 4 -A is the carboxylamine compound group, Figure 4 -B is a blank control group. From Figure 4 It can be seen that the state of the cells after adding the carboxylamine compound is not significantly different from that of the complete blank group, indicating that the compound has no biological toxicity.
Embodiment 2
[0041] Baby hamster kidney cells (BHK21) were cultured in DMEM medium containing 10% fetal calf serum at 37°C and 5% CO 2 When cultured in the environment until 90% confluence, 20 μl of vesicular stomatitis virus was added to the 6-well plate, and the culture was continued for 2 hours, and then the compound 2-imino-2H-chromene-3- Carboxamide was continued to be cultured in the coexistence environment of poison and drug, and the cytopathic state of BHK21 cells and the proliferation state of virus were observed after 24 hours.
[0042] Figure 5 To intervene the cytopathic effect 24 hours after VSV infects BHK21 with the dose of 5 μ l / well compound, wherein, Figure 5 -A: cell state after coexistence of poison and drug (5 μl / well) for 24 hours, Figure 5 -B: Infected and untreated control, Figure 5 -C: uninfected control group: from Figure 5 It can be seen that after the intervention of low-dose 2-imino-2H-chromene-3-carboxamide, compared with the non-drug-treated control ...
Embodiment 3
[0044] Baby hamster kidney cells (BHK21) were cultured in DMEM medium containing 10% fetal calf serum at 37°C and 5% CO 2 When cultured in the environment until 90% confluence, 20 μl of vesicular stomatitis virus was added to the 6-well plate, and the culture was continued for 2 hours, and then the compound 2-imino-2H-chromene-3- Carboxamide was continued to be cultured in the coexistence environment of poison and drug, and the cytopathic state of BHK21 cells and the proliferation state of virus were observed after 24 hours.
[0045] Figure 7 In order to intervene the cytopathic effect 24 hours after VSV infects BHK21 with the dose of 20 μ l / well compound, wherein, Figure 7 -A: cell state after coexistence of poison and drug (5 μl / well) for 24 hours, Figure 7 -B: Infected and untreated control, Figure 7 -C: uninfected control group: from Figure 7 It can be seen that after the intervention of a medium dose of 2-imino-2H-chromene-3-carboxamide, compared with the non-dru...
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