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精氨酰甘氨酰天门冬氨酸三肽的合成
引用本文:刘洪英,徐红岩,周乐.精氨酰甘氨酰天门冬氨酸三肽的合成[J].西北农业学报,2007,16(2):203-205.
作者姓名:刘洪英  徐红岩  周乐
作者单位:1. 西北农林科技大学生命科学学院,陕西杨凌,712100
2. 中国科学院上海有机化学研究所,上海,200032
摘    要:以L-精氨酸、L-甘氨酸、L-天门氨酸为原料,采用二环己基碳二亚胺(DCC)法合成了Arg-Gly-Asp(RGD)。Z-Arg(NO2)-OH经偶联剂活化与H-Gly-OMe.HCl缩合,水解后得到Z-Arg(NO2)-Gly-OH;产物与H-Asp(OBzl)-OBzl.TosOH偶联得到全保护多肽,经Pd-C/H2还原为Arg-Gly-Asp。

关 键 词:精氨酰甘氨酰天冬氨酸  三肽  偶联  二环己基碳二亚胺
文章编号:1004-1389(2007)02-0203-03
收稿时间:2006-09-21
修稿时间:2006-10-25

Synthesis of Tripeptide-RGD
LIU Hong-ying,XU Hong-yan and ZHOU Le.Synthesis of Tripeptide-RGD[J].Acta Agriculturae Boreali-occidentalis Sinica,2007,16(2):203-205.
Authors:LIU Hong-ying  XU Hong-yan and ZHOU Le
Institution:College of Life Sciences, Northwest A & F University, Yangling Shaanxi 712100 China;Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China;College of Life Sciences, Northwest A & F University, Yangling Shaanxi 712100 China
Abstract:Takintg L-Arginine,L-Glycine and L-Aspartate as a raw material,used DCC coupling method to synthesize Arg-Gly-Asp(R GD).Activating by coupling reagent,Z-Arg (NO2)-OH was coupled with H-GIy-OMe·HCl,after the hydrolysis Z-Arg(NO2)-Gly-OH was obtained;and then it was reacted with H-Asp (OBzl)-OBzl·TosOH to get complete protected tripeptide,at last using Pd C/H2 as reducing reagent,the final product Arg-Gly-Asp was obtained.
Keywords:Arg-Gly-Asp(RGD)  Tripeptide  Couple  DCC
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