Application of sulfamonomethoxine derivative in preparation of antitumor drugs
The technology of sulfamonomethoxine and antitumor drug is applied in the application field of sulfamonomethoxine derivatives in the preparation of antitumor drugs, and achieves the effects of good inhibitory effect, good application prospect and obvious inhibitory effect.
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Embodiment 1
[0041] Compound Sulfamono-methoxine (Sulfamono-methoxine), cpd-1, cpd-2, cpd-3, cpd-4 and cpd-5 inhibition of ALDOA activity assay:
[0042] The expressed and purified ALDOA protein was added to the 96-well plate according to different concentration gradients, and the ALDOA activity was determined by the aldolase activity colorimetric assay method. In particular ALDOA activity is determined by a colorimetric product whose absorbance at 450 nm is proportional to ALDOA activity. One unit of ALDOA is defined as the amount of enzyme that produces 1.0uM NADH per minute at a pH of 7.2 at 37°C ( figure 1 ).
Embodiment 2
[0043] Example 2: Compound Sulfamono-methoxine and cpd-5 inhibit ALDOA protein expression assay
[0044] Liver cancer, lung cancer, and pancreatic cancer cells were inoculated into 96-well plates at 1,000 cells per well, and cultured in 100 μl 10% FBS RPMI1640 culture medium. After culturing in an incubator for 24 hours, the cells were divided into groups, with 3 replicates in each group. Add the compounds Sulfamono-methoxine and cpd-5 in a 2-fold gradient, continue culturing until a specific detection time, collect the purified protein from the cells, add it to a 96-well plate that has been pre-bound with ALDOA antibody, add HRP-bound avidin for incubation, and add TMB Color development after the substrate solution, after adding sulfuric acid solution to terminate the enzyme substrate reaction, measure the color change at a wavelength of 450nm, and calculate the protein concentration of ALDOA after compound treatment ( figure 2 and image 3 ).
Embodiment 3
[0045] Example 3: Compound Sulfamono-methoxine and cpd-5 inhibit tumor cell viability assay
[0046] Liver cancer, lung cancer, and pancreatic cancer cells were inoculated into 96-well plates at 1,000 cells per well, and cultured in 100 μl 10% FBS RPMI1640 culture medium. After culturing in an incubator for 24 hours, the cells were divided into groups, with 3 replicates in each group. Add compounds Sulfamono-methoxine and cpd-5 in a 2-fold gradient and continue culturing until a specific detection time, add 10 μl CCK8 to each well, and incubate for 0.5-4 hours depending on the cells, use a microplate reader to detect cell viability at a wavelength of 450 nm, and calculate IC50( Figure 4 and Figure 5 ).
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