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Collect. Czech. Chem. Commun. 1967, 32, 843-853
https://doi.org/10.1135/cccc19670843

Amino acids and peptides. LXVIII. Preparation of three lysine-vasopressin analogs modified at position 9; D-Ala9-lysine-vasopressin, Ala9-lysine-vasopressin, and 9-ethylenediamine-lysine-vasopressin

M. Zaoral, J. Kolc, F. Korenczki, V. P. Černěckij and F. Šorm

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  • Kamphuis J., Boesten W. H. J., Schoemaker H. E., Aubry A., Bayeul D., Dautant A., Pantano M., Formaggio F., Crisma M., Bonora G. M., Toniolo C.: Peptides from chiral Cα,α-disubstituted glycines. Synthesis and conformational analysis of homochiral (αMe) Leu / Ala model peptides. Recl. Trav. Chim. Pays-Bas 2010, 113, 29. <https://doi.org/10.1002/recl.19941130104>
  • Buku Angeliki, Gazis Diana, Schwartz Irving L.: Antidiuretic and pressor activities of vasopressin analogs with L-alaninamide and D-alaninamide substitutions at position 9. International Journal of Peptide and Protein Research 2009, 23, 551. <https://doi.org/10.1111/j.1399-3011.1984.tb02757.x>
  • MaGee David I., Ramaseshan Mahesh, Leach James D.: Synthesis of cyclic and acyclic imides, sulfonimides, and N-carbobenzyloxyamides by ketene trapping. Can. J. Chem. 1995, 73, 2111. <https://doi.org/10.1139/v95-260>
  • Herdeis Claus, Gebhard Rolf: Aminosäuren. 8. Mitt. Peptidsynthesen mit (±) 5-Hydroxy-2-pyridylglycin ((±) Pyg (5-OH)), einer neuen heterocyclisch substituierten Aminosäure. Arch. Pharm. Pharm. Med. Chem. 1987, 320, 546. <https://doi.org/10.1002/ardp.19873200612>
  • Fastrez Jacques, Fersht Alan R.: Demonstration of the acyl-enzyme mechanism for the hydrolysis of peptides and anilides by chymotrypsin. Biochemistry 1973, 12, 2025. <https://doi.org/10.1021/bi00735a001>