Cholic acid modified amphiphilic pyrene derivative fluorescent probe as well as synthesis method and application thereof
A technology of fluorescent probes and pyrene derivatives, which is applied in the field of protein detection, can solve the problems of low sensitivity, strong hydrophobicity, limited application of biological detection object sensing, etc., and achieves the effects of low equipment requirements and simple operation.
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Embodiment 1
[0060] A fluorescent probe based on cholic acid-modified amphiphilic pyrene derivatives was synthesized with the following structural formula:
[0061]
[0062] Its synthetic method comprises the following steps:
[0063] 1) Synthesis of pyrenesulfonyl derivatives
[0064] Under the conditions of nitrogen protection and ice-bath stirring at a flow rate of 0.6-0.8mL / s, 1.47mL (9.97mmol) of 1,8-diamino-3,6-diox octane, and then 0.30 g (0.997 mmol) of pyrenesulfonyl chloride was dissolved in 40 mL of chloroform and added dropwise to the above solution. After the dropwise addition, stir at room temperature for 2 hours. After stopping the reaction, wash the reaction solution with saturated brine for 6 to 7 times, then dry it with anhydrous sodium sulfate overnight, distill off chloroform, and use dichloromethane and methanol at a volume ratio of The mixed solvent of 30:1 is used as eluent column chromatography purification product, obtains the pyrenesulfonyl derivative shown i...
Embodiment 2
[0074] A fluorescent probe based on cholic acid-modified amphiphilic pyrene derivatives was synthesized with the following structural formula:
[0075]
[0076] Its synthetic method step is as follows:
[0077] In step 1 of the synthesis of pyrenesulfonyl derivatives in Example 1, the 1,8-diamino-3,6-dioxoctane used was replaced with 3,6,9-trioxaundecane with an equimolar mass - 1,11-diamine replacement, other steps are the same as the corresponding Example 1.
Embodiment 3
[0079] A fluorescent probe based on cholic acid-modified amphiphilic pyrene derivatives was synthesized with the following structural formula:
[0080]
[0081] In step 1 of the synthesis of pyrenesulfonyl derivatives in Example 1, the 1,8-diamino-3,6-dioxoctane used was mixed with 3,6,9,12-tetraoxadecane of equimolar mass Hexane-1,16-diamine was replaced, and other steps were the same as the corresponding Example 1.
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