Ruthenium-containing complex for inhibiting protein tyrosine phosphatase 1B activity as well as preparation method of complex and protein tyrosine phosphatase 1B inhibitor
A technology of tyrosine phosphatase and ruthenium complexes, which can be applied to compounds containing elements of Group 8/9/10/18 of the periodic table, chemical instruments and methods, drug combinations, etc., can solve the problem of hindering lung metastasis and delaying tumors development process and other issues to achieve a good inhibitory effect
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Embodiment 1
[0043] This example is used to illustrate the preparation of the ruthenium-containing complex for inhibiting the activity of protein tyrosine phosphatase 1B of the present invention.
[0044]
[0045] (1) In the mixed solution of liquid ammonia and ethanol, at -78°C, mix the aromatic hydrocarbon with metal sodium for 1 hour (the molar ratio of liquid ammonia, ethanol, aromatic hydrocarbon and sodium is 250:10:1:5), to obtain Dihydrogenated aromatic hydrocarbons; the aromatic hydrocarbons are p-methylcymene; then the reaction product is subjected to vacuum distillation at 50-150°C to remove the solvent and some unreacted raw materials, and it is obtained by nuclear magnetic resonance analysis. In the reaction product mixture , the purity of dihydroaromatics is about 70% by weight;
[0046] (2) The reaction product mixture containing dihydroaromatics and ruthenium chloride are contacted in ethanol, wherein, the consumption of the reaction product mixture containing dihydroaro...
Embodiment 2
[0052] This example is used to illustrate the inhibitory activity of ruthenium-containing complexes on protein tyrosine phosphatase 1B (PTP1B).
[0053] In this example, dithiothreitol (DTT) was purchased from Pierce Company, MOPS was purchased from AMRESCO Company, pNPP was purchased from Alfa Company, and NaOH was purchased from Beijing Chemical Reagent Company, all of which were of analytical grade.
[0054] First, 10 μL of ruthenium compounds with different concentrations (200 μM, 100 μM, 10 μM, 1 μM, 0.1 μM and 0.01 μM, respectively, 6 samples for each concentration) were added to 70 μL of 20 mM MOPS buffer, and PTP1B was added, and the amount of PTP1B added was such that The final concentration of PTP1B in the mixture was 250nM. After the mixture was incubated at 25°C for 30min, 5 μL of DTT (DTT concentration was 2mM) was added, and incubated at the same temperature for another 30min to maintain the activity of the enzyme. Then 10 uL of pNPP (0.02M) substrate was added. ...
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