Synthesis of Cyclic Antifreeze Glycopeptide and Glycopeptoids and Their Ice Recrystallization Inhibition Activity

被引:5
作者
Ahn, Mija [2 ]
Murugan, Ravichandran N. [2 ]
Shin, Song Yub [3 ,4 ]
Kim, Eunjung [1 ]
Lee, Jun Hyuck [1 ,5 ]
Kim, Hak Jun [1 ,5 ]
Bang, Jeong Kyu [2 ]
机构
[1] Korea Polar Res Inst, Div Polar Life Sci, Inchon 406840, South Korea
[2] Korea Basic Sci Inst, Div Magnet Resonance, Chung Buk 363883, South Korea
[3] Chosun Univ, Grad Sch, Dept Biomat, Kwangju 501759, South Korea
[4] Chosun Univ, Sch Med, Dept Cellular & Mol Med, Kwangju 501759, South Korea
[5] Univ Sci & Technol, Dept Polar Sci, Inchon 406840, South Korea
来源
BULLETIN OF THE KOREAN CHEMICAL SOCIETY | 2012年 / 33卷 / 11期
关键词
Cyclic glycopeptide; Ice recrystallization inhibition; Solid phase synthesis; Cyclic glycopeptoid; GLYCOPROTEIN AFGP; DROSOCIN;
D O I
10.5012/bkcs.2012.33.11.3565
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Until now, few groups reported the antifreeze activity of cyclic glycopeptides; however, the tedious synthetic procedure is not amenable to study the intensive structure activity relationship. A series of N-linked cyclic glycopeptoids and glycopeptide have been prepared to evaluate antifreeze activity as a function of peptide backbone cyclization and methyl stereochemical effect on the rigid Thr position. This study has combined the cyclization protocol with solid phase peptide synthesis and obtained significant quantities of homogeneous cyclic glycopeptide and glycopeptoids. Analysis of antifreeze activity revealed that our cyclic peptide demonstrated RI activity while cyclic glycopeptoids showed no RI activity. These results suggest that the subtle changes in conformation and Thr orientation dramatically influence RI activity of N-linked glycopeptoids
引用
收藏
页码:3565 / 3570
页数:6
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