首页 | 本学科首页   官方微博 | 高级检索  
     


Di-oxanipecotic acids as more stable turn motifs than di-nipecotic acids
Authors:Bong-hyeon BaekMyung-ryul Lee  Kwang-Yon KimUng-In Cho  Doo Wan Boo  Injae Shin
Affiliation:Department of Chemistry, Yonsei University, Seoul 120-749, Republic of Korea
Abstract:The folded structures of peptidomimetics containing dimers of oxanipecotic acid (Oxa) in loop segments were characterized and compared with those of the corresponding nipecotic acid (Nip)-based ones. According to structural studies using FT-IR and NMR spectroscopies, di-oxanipecotic acid adopted more stable turn conformations than di-nipecotic acid, and for tetramers, L,(S)-Oxa,(S)-Oxa,L and L,(S)-Oxa,(R)-Oxa,L formed hairpin-like structures but only L,(R)-Nip,(S)-Nip,L promoted the stable folded conformations.
Keywords:amino acids and derivatives   coupling reactions   hydrogen bonding   peptide analogues/mimetics
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号