A kind of peptoid and its preparation method and application
A kind of synthetic method technology, applied in the field of biomedicine, can solve the problems of lack of accuracy and specificity of the method, and achieve the effect of good specificity, low cost and simple synthesis
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Embodiment 1
[0044] The preparation of embodiment 1 class peptide
[0045] The peptoids of the present invention are synthesized by solid-phase subunit synthesis, and the method comprises the following steps:
[0046] (1) Add 2M bromoacetic acid and 3.2M N,N'-diisopropylcarbodiimide (DIC) to Rink amide AM resin (substitution level 0.3mmol / g), react at 37°C for 30min, and the resin terminal Amino acylation;
[0047] (2) Add 2M primary amine and react at 37°C for 90 minutes to replace the bromine atom through a nucleophilic substitution reaction to complete the synthesis of a subunit;
[0048] (3) Steps (1) and (2) are repeated until the synthesis of the remaining units is completed;
[0049] (4) After the synthesis is completed, the side chain protecting group is removed, and the peptoid is cleaved from the resin with 95% trifluoroacetic acid, 2.5% ultrapure water, and 2.5% triisopropylsilane for future use.
[0050] The molecular formula of the prepared peptoid is as follows:
[0051] ...
Embodiment 2
[0053] The preparation of embodiment 2 class peptides
[0054] The peptoids of the present invention are synthesized by solid-phase subunit synthesis, and the method comprises the following steps:
[0055] (1) Add 2M bromoacetic acid and 3.2M N,N'-diisopropylcarbodiimide (DIC) to Rink amide AM resin (substitution level 0.3mmol / g), react at 37°C for 30min, and the resin terminal Amino acylation;
[0056] (2) Add 2M primary amine and react at 37°C for 90 minutes to replace the bromine atom through a nucleophilic substitution reaction to complete the synthesis of a subunit;
[0057] (3) Steps (1) and (2) are repeated until the synthesis of the remaining units is completed;
[0058] (4) After the synthesis is completed, the side chain protecting group is removed, and the peptoid is cleaved from the resin with 95% trifluoroacetic acid, 2.5% ultrapure water, and 2.5% triisopropylsilane for future use.
[0059] The molecular formula of the prepared peptoid is as follows:
[0060]...
Embodiment 3
[0062] The preparation of embodiment 3 class peptides
[0063] The peptoids of the present invention are synthesized by solid-phase subunit synthesis, and the method comprises the following steps:
[0064] (1) Add 2M bromoacetic acid and 3.2M N,N'-diisopropylcarbodiimide (DIC) to Rink amide AM resin (substitution level 0.3mmol / g), react at 37°C for 30min, and the resin terminal Amino acylation;
[0065] (2) Add 2M primary amine and react at 37°C for 90 minutes to replace the bromine atom through a nucleophilic substitution reaction to complete the synthesis of a subunit;
[0066] (3) Steps (1) and (2) are repeated until the synthesis of the remaining units is completed;
[0067] (4) After the synthesis is completed, the side chain protecting group is removed, and the peptoid is cleaved from the resin with 95% trifluoroacetic acid, 2.5% ultrapure water, and 2.5% triisopropylsilane for future use.
[0068] The molecular formula of the prepared peptoid is as follows:
[0069]...
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