Chemically modified thymosin α1 and its synthesis method

A technology of chemical modification and synthesis method, which is applied in the direction of chemical instruments and methods, thymosin, and peptide preparation methods. It can solve the problems of large molecular weight of PEG, difficulty in obtaining modified site products, and decreased biological activity of drugs, so as to achieve bioavailability. High, increased duration, extended half-life effects

Active Publication Date: 2019-01-15
SHENZHEN INST OF ADVANCED TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The disadvantage of PEG modification in the chemical modification method is that since PEG itself is a polymer, it is difficult to obtain a product with a precise modification site and a unique chemical structure of the product
In addition, the molecular weight of PEG is large, and the biological activity of the modified drug is greatly reduced.

Method used

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  • Chemically modified thymosin α1 and its synthesis method
  • Chemically modified thymosin α1 and its synthesis method
  • Chemically modified thymosin α1 and its synthesis method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] The synthetic method of the thymosin α1 of embodiment 1 chemical modification

[0039] Include the following steps:

[0040] (1) Weigh 200 mg of Fmoc-protected asparagine king resin (Fmoc-Asn(Trt)-WangResin 0.12 mmol / g) into a manual solid-phase peptide synthesizer, add DCM (dichloromethane) to swell for 30 minutes. Using Fmoc-protected amino acid raw materials, benzotriazole-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU) and diisopropylethylamine (DIEA) as peptide condensation Mixture, the equivalent ratio of resin and each protected amino acid and polypeptide condensing agent is tyrosine king resin: amino acid: HBTU: DIEA=1: 3: 3: 6, according to the standard Fmoc strategy synthesis Fmoc protects the king loaded with thymosin α1 Resin (Compound 1).

[0041] (2) After removing the terminal amino Fmoc protecting group with 2 ml of piperidine deprotecting agent (piperidine: DMF = 20:80 (v / v), dissolve 46 mg of myristic acid (0.2 mmol) in 2 ml Dimethylformamid...

Embodiment 2

[0046] The synthetic method of the thymosin α1 of embodiment 2 chemical modifications

[0047] Include the following steps:

[0048] (1) Weigh 200 mg of Fmoc-protected asparagine king resin (Fmoc-Asn(Trt)-WangResin 0.12 mmol / g) into a manual solid-phase peptide synthesizer, add DCM (dichloromethane) to swell for 30 minutes. Sequentially use Fmoc-protected amino acid raw materials (where the fourteenth position uses Fmoc-Lys(Dde)-OH), and use benzotriazole-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU) and diisopropylethylamine (DIEA) are polypeptide condensing agents, and the equivalent ratio of resin and each protected amino acid and polypeptide condensing agent is tyrosine king resin: amino acid: HBTU: DIEA=1: 3: 3: 6. Synthesize Fmoc-protected Wang resin loaded with thymosin α1 according to the standard Fmoc strategy. Subsequently, 2 ml of piperidine deprotecting agent (piperidine: DMF = 20: 80) was used to remove the Fmoc protecting group of the terminal amino g...

Embodiment 3

[0053] The synthetic method of the thymosin α1 of embodiment 3 chemical modifications

[0054] Include the following steps:

[0055] (1) Dissolve myristic acid (460 mg, 2 mmol) in 100 ml of dichloromethane (DCM), activate with equivalent HBTU (759 mg, 2 mmol) and DIEA (260 mg, 2 mmol) for 2 minutes, add Fmoc-Lys-OH (736 mg, 2 mmol), after reacting at room temperature for 1 hour, the DCM was evaporated under reduced pressure, and the crude product was purified by HPLC to obtain the lysine (Fmoc-Lys(Myristic acid) of the myristic acid modified side chain of Fmoc protection. )-OH) 872 mg, the yield was 76%. The reaction equation is as follows:

[0056]

[0057] (2) Weigh 200 mg of Fmoc-protected asparagine king resin (Fmoc-Asn(Trt)-WangResin 0.12 mmol / g) into a manual solid-phase peptide synthesizer, add DCM (dichloromethane) to swell for 30 minutes. Sequentially use Fmoc-protected amino acid raw materials (where the fourteenth position uses Fmoc-Lys(Myr)-OH), and use benzo...

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Abstract

The invention discloses a chemically modified thymulin alpha 1 and a synthetic method thereof. The structure of the chemically modified thymulin alpha 1 is shown as follows: A-Ser-Asp-Ala-Ala-Val-Asp-Thr-Ser-Ser-Glu-IIe-Thr-Thr-Lys-Asp-Leu-Lys-Glu-Lys-Lys-Glu-Val-Val-Glu-Glu-Ala-Glu-Asn-OH or Ac-Ser-Asp-Ala-Ala-Val-Asp-Thr-Ser-Ser-Glu-IIe-Thr-Thr-Lys(A)-Asp-Leu-Lys-Glu-Lys-Lys-Glu-Val-Val-Glu-Glu-Ala-Glu-Asn-OH. The A is an aliphatic acid bonding in affinity with human serum albumin, or is a maleimide derivative coupled with free sulfydryl of human serum albumin. The chemically modified thymulin alpha 1 has characteristics of precision modification sites, a definite chemical structure and a simple and concise synthetic process. The chemically modified thymulin alpha 1 after being injected intravenously bonds immediately with the serum albumin of the human body and adopts the serum albumin of the human body as a controlled-release vector, thus prolonging the half-life period largely, and significantly prolonging the time of duration of the effective medicine concentration. The bioavailability is high.

Description

technical field [0001] The invention belongs to the field of synthesis of biochemical materials, and more specifically, the invention relates to a chemically modified thymosin α1 and a synthesis method thereof. Background technique [0002] Thymosin α1 is a chemically synthesized polypeptide drug with higher biological activity than animal-derived thymosin. Thymosin α1 is widely used as an immune enhancer in the immunotherapy of severe infection, hepatitis and tumor. [0003] Pharmacokinetic studies show that thymosin α1 is quickly degraded by protease and aminopeptidase in human plasma, with a half-life of about 1.65 hours. The current clinical preparation is thymosin α1 freeze-dried powder for injection, so the half-life is very short, it is easily degraded by enzymes in plasma and loses biological activity, and the bioavailability is very low. Repeated and long-term injections are required for clinical use. And other defects are the main problem of thymosin α1 products ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07K14/575C07K1/107C07K1/06C07K1/04
CPCC07K14/57581C07K19/00
Inventor 粟武
Owner SHENZHEN INST OF ADVANCED TECH
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