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Collect. Czech. Chem. Commun. 1990, 55, 1099-1105
https://doi.org/10.1135/cccc19901099

Synthesis and biological properties of vasopressin analogues containing 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Zdenko Procházkaa, Juris E. Ancansa, Jiřina Slaninováa, Alena Machováb, Tomislav Bartha and Michal Lebla

a Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6
b Research Institute for Pharmacy and Biochemistry, 130 00 Prague 3

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  • Jastrzȩbska B., Derdowska I., Kowalczyk W., Machova A., Slaninová J., Lammek B.: Influence of 1‐aminocyclohexane‐1‐carboxylic acid in position 2 or 3 of AVP and its analogues on their pharmacological properties. The Journal of Peptide Research 2003, 62, 70. <https://doi.org/10.1034/j.1399-3011.2003.00069.x>
  • Ślusarz R., Kaźmierkiewicz R., Lammek B.: Theoretical conformational analysis of six arginine vasopressin analogs with the l‐naphthylalanine in position 3. The Journal of Peptide Research 2000, 56, 352. <https://doi.org/10.1034/j.1399-3011.2000.00743.x>
  • Stoev S., Cheng L.L., Olma A., Klis W.A., Manning M., Sawyer W.H., Wo N.C., Chan W.Y.: An investigation of position 3 in arginine vasopressin with aliphatic, aromatic, conformationally-restricted, polar and charged amino acids. J Peptide Sci 1999, 5, 141. <https://doi.org/10.1002/(SICI)1099-1387(199903)5:3<141::AID-PSC180>3.0.CO;2-6>
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  • Manning Maurice, Cheng Ling Ling, Stoev Stoytcho, Klis Wieslaw A., Nawrocka Eleonora, Olma Aleksandra, Sawyer Wilbur H., Wo Nga Ching, Chan W. Y.: Position Three in Vasopressin Antagonist Tolerates Conformationally Restricted and Aromatic Amino Acid Substitutions: A Striking Contrast with Vasopressin Agonists. J Peptide Sci 1997, 3, 31. <https://doi.org/10.1002/(SICI)1099-1387(199701)3:1<31::AID-PSC82>3.0.CO;2-Y>
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