Conformations of psi [CH2NH] pseudopeptides. Cyclo[Gly-Pro psi [CH2NH]Gly-D-Phe-Pro]-TFA and cyclo[Gly-Pro psi [CH2NH]Gly-D-Phe-Pro].

S Ma, A F Spatola
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Abstract

The cyclic pseudopentapeptide cyclo[Gly-Pro psi [CH2NH]Gly-D-Phe-Pro] and its TFA salt were synthesized by solution methods, and their conformations were studied by NMR spectroscopy in both DMSO-d6 and CDCl3. While intramolecular hydrogen bonding is observed with some conformers, the nature of the solvent and the presence of TFA affects the relative structural rigidities of the compounds. No evidence was found for the psi [CH2NH] or psi [CH2NH2+] units acting as H donors in this series.

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psi [CH2NH]伪多肽的构象。Cyclo[Gly-Pro psi [CH2NH]Gly-D-Phe-Pro]-TFA和Cyclo[Gly-Pro psi [CH2NH]Gly-D-Phe-Pro]。
采用溶液法合成了环状伪五肽环环[Gly-Pro psi [CH2NH]Gly-D-Phe-Pro]及其TFA盐,并利用核磁共振波谱在DMSO-d6和CDCl3中研究了它们的构象。虽然在某些构象中观察到分子内氢键,但溶剂的性质和TFA的存在影响了化合物的相对结构刚度。在这个系列中没有发现psi [ch2nhh]或psi [CH2NH2+]单位作为H供体的证据。
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