Enzymatic Synthesis of a CCK-8 Tripeptide Derivative

Li GUO Zi Min LU Heiner ECKSTEIN

引用本文: Li GUO,  Zi Min LU,  Heiner ECKSTEIN. Enzymatic Synthesis of a CCK-8 Tripeptide Derivative[J]. Chinese Chemical Letters, 2003, 14(2): 167-168. shu
Citation:  Li GUO,  Zi Min LU,  Heiner ECKSTEIN. Enzymatic Synthesis of a CCK-8 Tripeptide Derivative[J]. Chinese Chemical Letters, 2003, 14(2): 167-168. shu

Enzymatic Synthesis of a CCK-8 Tripeptide Derivative

摘要: The enzymatic synthesis of CCK-8 tripeptide derivative Phac-Met-Asp(OMe)-Phe-NH2 is reported.Starting with Phac-Met-OCam, we have successfully synthesized the target tripeptide with three free or immobilized enzymes, α-chymotrypsin, papain and thermolysin in reasonable yields.The key steps in this synthesis were the coupling of Phac-Met-OCam and H-Asp(OMe)2 to form Met-Asp peptide bond catalyzed by α-chymotrypsin and the selective hydrolysis of α-ester of Phac-Met-Asp(OMe)2 catalyzed by papain.

English

  • 加载中
计量
  • PDF下载量:  0
  • 文章访问数:  1012
  • HTML全文浏览量:  18
文章相关
  • 收稿日期:  2002-05-20
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章