ENZYMIC-SYNTHESIS OF OPIOID PEPTIDES

被引：30

作者：

WONG, CH ^{[1
]}

CHEN, ST ^{[1
]}

WANG, KT ^{[1
]}

机构：

[1] ACAD SINICA,INST BIOL CHEM,TAIPEI,TAIWAN

来源：

BIOCHIMICA ET BIOPHYSICA ACTA | 1979年 / 576卷 / 01期

关键词：

Enzymic synthesis; Opioid peptide; Papain catalyst;

D O I：

10.1016/0005-2795(79)90500-2

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Protected opioid pentapeptides were synthesized by the papain-catalyzed condensation of small synthetic fragments. These peptides, free as well as protected, were identical with those prepared by the dicyclohexylcarbodiimide-1-hydroxybenzotriazole method. © 1979.

引用

页码：247 / 249

页数：3

共 12 条

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[6] ENZYMATIC-SYNTHESIS OF PROTECTED VALINE-5 ANGIOTENSIN 2 AMIDE-1
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[7] SYNTHESIS OF PEPTIDES BY MEANS OF PROTEOLYTIC-ENZYMES
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[8] A NEW METHOD FOR SYNTHESIS OF PEPTIDES - ACTIVATION OF CARBOXYL GROUP WITH DICYCLOHEXYLCARBODIIMIDE USING 1-HYDROXYBENZOTRIAZOLES AS ADDITIVES
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GEIGER, R
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[9] ALPHA-CHYMOTRYPSIN AS CATALYST FOR PEPTIDE-SYNTHESIS
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OKA, T
[J]. BIOCHEMICAL JOURNAL, 1977, 163 (03) : 531 - 542
[10] TRYPSIN AS A CATALYST FOR PEPTIDE-SYNTHESIS
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[J]. JOURNAL OF BIOCHEMISTRY, 1977, 82 (04) : 1055 - 1062

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