Nsc and Fmoc Nα-amino protection for solid-phase peptide synthesis:: a parallel study

被引:16
作者
Carreño, C
Méndez, ME
Kim, YD
Kim, HJ
Kates, SA
Andreu, D
Albericio, F
机构
[1] Univ Barcelona, Dept Organ Chem, Peptide Synth Facil, E-08028 Barcelona, Spain
[2] Univ Barcelona, Dept Organ Chem, E-08028 Barcelona, Spain
[3] Hyundai Pharm Ind Co Ltd, Res Inst, Buchon, South Korea
[4] PerSept Biosyst Inc, Framingham, MA 01701 USA
来源
JOURNAL OF PEPTIDE RESEARCH | 2000年 / 56卷 / 02期
关键词
difficult sequences; polyproline; protected peptides; racemization;
D O I
10.1034/j.1399-3011.2000.00711.x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The 2-(4-nitrophenylsulfonyl)ethoxycarbonyl (Nsc) group is an alternative to Fmoc for N-alpha-protection in solid-phase peptide synthesis. Nsc-amino acids may be particularly suitable for automatic synthesizers, in which the amino acids are stored in solution, and the incorporation of residues prone to racemization such as Cys and His. Owing to the hydrophilicity of the Nsc group, these derivatives are useful for the preparation of protected peptides in convergent solid-phase peptide synthesis strategies.
引用
收藏
页码:63 / 69
页数:7
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