Solid-phase synthesis of ATL peptides

A solid-phase synthesis and solid-phase carrier technology, which is applied in the preparation methods of peptides, chemical instruments and methods, peptides, etc., can solve the problems of long production cycle, human injury, unsuitable for large-scale preparation and industrial production, etc.

A solid-phase synthesis and solid-phase carrier technology, which is applied in the preparation methods of peptides, chemical instruments and methods, peptides, etc., can solve the problems of long production cycle, human injury, unsuitable for large-scale preparation and industrial production, etc.

CN101255187BInactive Publication Date: 2011-09-07济南环肽医药科技有限公司
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  • Solid-phase synthesis of ATL peptides
  • Solid-phase synthesis of ATL peptides
  • Solid-phase synthesis of ATL peptides

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] h 2 Preparation of N-Lys(2-Cl-Z)-MBHA

[0043] (1) Put 50g (40mmol) of MBHA resin in a polypeptide synthesis reactor, wash it twice with 5% triethylamine DCM solution 5-7ml / g, each time for 8 minutes; alternately wash with 300ml each of dichloromethane and ethanol 2 times, 2 minutes / time, drain.

[0044] (2) Mix Boc-Lys(2-Cl-Z)-OH 82.8g and HOBt 27.0g, N,N-cyclohexylcarbodiimide 41.2g with 500ml dichloromethane / DMF solution (dichloromethane:N, N-dimethylformamide (volume ratio: 1:0.8) was dissolved, added to the resin, stirred at room temperature for 5 hours, and drained.

[0045] (3) The product of (2) was alternately washed 3 times with 300 ml of dichloromethane and 300 ml of ethanol, each time for 2 minutes, and drained.

[0046] (4) Wash once with 50% trifluoroacetic acid / dichloromethane (DCM) 10ml / g for 20 minutes; wash twice with dichloromethane 5-7ml / g for 2 minutes each time; get: H 2 N-Lys(2-Cl-Z)-MBHA.

Embodiment 2

[0048] h 2 Preparation of N-Lys(2-Cl-Z)-Lys(2-Cl-Z)-MBHA

[0049] (1) to resin H 2 Add 5% triethylamine DCM solution 5-7ml / g to N-Lys(2-Cl-Z)-MBHA and wash twice, 8 minutes each time; alternately wash twice with 300ml dichloromethane and ethanol, 2 minutes / times, drained.

[0050] (2) Mix Boc-Lys(2-Cl-Z)-OH 82.8g and HOBt 27.0g, N,N-cyclohexylcarbodiimide 41.2g with 500ml dichloromethane / DMF solution (dichloromethane:N, N-dimethylformamide (volume ratio: 1:0.9) was dissolved, added to the resin, stirred at room temperature for 5 hours, and drained.

[0051] (3) The product of (2) was alternately washed 3 times with 300 ml of dichloromethane and 300 ml of ethanol, each time for 2 minutes, and drained.

[0052] (4) Wash once with 50% trifluoroacetic acid / dichloromethane (DCM) 10ml / g for 20 minutes;

[0053] Wash twice with dichloromethane 5-7ml / g, 2 minutes each time;

[0054] Got: H 2 N-Lys(2-Cl-Z)-Lys(2-Cl-Z)-MBHA.

Embodiment 3

[0056] h 2 Preparation of N-Lys(2-Cl-Z)-Lys(2-Cl-Z)-Lys(2-Cl-Z)-MBHA

[0057] Operation: (1) to resin H 2 Add 5% triethylamine DCM solution 5-7ml / g to N-Lys(2-Cl-Z)-Lys(2-Cl-Z)-MBHA and wash twice, each time for 8 minutes; Each 300ml was alternately washed twice, 2 minutes each time, and drained.

[0058] (2) Mix Boc-Lys(2-Cl-Z)-OH 82.8g and HOBt 27.0g, N,N-cyclohexylcarbodiimide 41.2g with 500ml dichloromethane / DMF (dichloromethane:N,N - dimethylformamide (volume ratio: 1:0.9) solution was dissolved, added to the resin, stirred at room temperature for 5 hours, and drained.

[0059] (3) The product of (2) was alternately washed 3 times with 300 ml of dichloromethane and 300 ml of ethanol, each time for 2 minutes, and drained.

[0060] (4) Wash once with 50% trifluoroacetic acid / dichloromethane (DCM) 10ml / g for 20 minutes;

[0061] Wash twice with dichloromethane 5-7ml / g, 2 minutes each time;

[0062] Got: H 2 N-Lys(2-Cl-Z)-Lys(2-Cl-Z)-Lys(2-Cl-Z)-MBHA.

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Abstract

The invention discloses a solid phase synthesis process for a ATL peptide. The process comprises using MBHA resin as a solid phase carrier, combines protective lysyl Boc-Lys(2-Cl-Z) on the resin, completing the synthesis of ATL by stepwise peptide combining method for protecting aminophenol with Boc, modifying N end with acetic anhydride by acetylizing to obtain all-protected peptide resin; depriving the side chain protecting group of the formacyl of Trp with piperidine, and at last, depriving side chain protection group with fluoroform sulfonic acids and incising the resin to obtain ATL coarse peptide; and then purifying the crude product with the highly effective liquid phase of reversed phase C18 filler, separating and purifying with methanol-water gradient eluting process to obtain ATLpeptide refining product. The process of the invention with single-step condensation reaction has high yield and low by-product, and the final crude product has high purity and small impurity content, the operation is simple, and the total yield is high.

Description

technical field [0001] The present invention relates to the preparation method of polypeptide medicine, relate in particular to a kind of ATL peptide (C 85 H 141 N 27 O 15 ) of the solid-phase synthesis method. It belongs to the field of biotechnology. Background technique [0002] ATL peptide chemical name: acetyl-arginyl-tyrosyl-tyrosyl-arginyl-tryptophanyl-lysyl-lysyl-lysyl-lysyl-lysyl-lysyl-lysyl -Lysinamide (Ac-Arg-Tyr-Tyr-Arg-Trp-Lys-Lys-Lys-Lys-Lys-Lys-Lys-NH 2 ), [0003] The chemical structural formula is: [0004] [0005] Molecular formula: C 85 H 141 N 27 O 15 [0006] Molecular weight: 1781.24. [0007] ATL peptide is in Ac-RYYRWK-NH 2 The hexapeptide was remodeled on the basis of the hexapeptide, which was selectively screened by NOP (Nociceptin / orphanin FQ peptide receptor) from the synthetic combinatorial chemical peptide library. Orphanin (nocieeptin or orphanin FQ) is an endogenous ligand for opioid receptor-like receptors (ORL1 or LC 132)...

Claims

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Application Information

Patent Timeline
07 Sep 2011
Publication
CN101255187B
IPC
C07K1/04; C07K1/06
CPC
Y02P20/55
Inventors
厉保秋