Preparation method and antineoplastic activity of novel ruthenium complex containing 4,4'-dibromo-2,2'-dipyridyl
A technology of complexes and anti-cancer activity, applied in containing 4, can solve the problems of low water solubility, large toxic and side effects, drug resistance of cancer cells, etc., and achieve the effect of enhancing binding ability and high affinity
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Embodiment 1
[0020] A compound containing 2,3-bis(4-nitrophenyl)pyrazine[2,3-f][1,10]phenanthroline and 4,4'-dibromo-2,2'-bipyridine The synthesis of novel Ru (II) complex comprises the following process steps:
[0021] (1) Synthesis of 4-nitrobenzoin
[0022] Put 20mL of 4-nitrobenzaldehyde and 30mL of absolute ethanol into a 250mL three-necked flask, stir, add 7mL of an aqueous solution containing 3.5g of vitamin B1 (8.75mmol), and adjust the pH of the reaction system to 8-9 with 3mol / L NaOH solution , After stirring for 1 h, let it stand at room temperature for more than 24 h. When a large amount of white solids are precipitated, filter with suction, and rinse the filter cake with deionized water three times (20 mL×3). After the solid was dried, it was recrystallized with absolute ethanol to obtain 15.4 g of white needle-like crystals with a yield of 76.9%. The reaction formula was:
[0023]
[0024] (2) Synthesis of 4-nitrobenzil
[0025] Add 2.10 g of 4-nitrobenzoin (10 mmol), ...
Embodiment example 2
[0036] Implementation Case 2: Anti-tumor activity experiment of Ru(II) complexes
[0037]The invention adopts the MTT method to measure the toxicity of Ru(II) complexes to tumor cells in vitro, and takes liver cancer cell line Hep G2 and human melanoma cell line F10-B16 as detection objects. The cultured cancer cell suspension was inoculated into a clean 96-well culture plate, 200 μL / well, and the obtained Ru(II) complex was added to the cell culture plate in a concentration gradient (6.25 μM-100 μM), and each Well 100 μL, the concentration of each Ru(II) complex is 2 parallel plates, the blank control group does not add Ru(II) complex, only culture solution is added. Place in a 37°C incubator at a constant temperature for 48 hours, add 20 μL of 5 g / L MTT to each well, continue to incubate for 5 hours, then add 100 μL of SDS to each well, and measure the absorbance value of each well at a wavelength of 570 nm on a microplate reader after 10 hours. The inhibition rate was calc...
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