Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1972, 37, 1539-1545
https://doi.org/10.1135/cccc19721539

Amino acids and peptides. CVI. Cyclic part of vasopressin and oxytocin molecule; Synthesis and biological properties

M. Zaoral and M. Flegel

Crossref Cited-by Linking

  • Barth Tomislav, Le Bars Noelle-Claire, Roy Christian, Jard Serge: Hydro-osmotic activity of ‘carba’ analogues of oxytocin and [8-Arginine] vasopressin on frog (Rana esculenta) bladder. European Journal of Pharmacology 1975, 32, 214. <https://doi.org/10.1016/0014-2999(75)90285-X>
  • Roy C, Barth T, Jard S: Vasopressin-sensitive kidney adenylate cyclase. Structural requirements for attachment to the receptor and enzyme activation: studies with vasopressin analogues. Journal of Biological Chemistry 1975, 250, 3149. <https://doi.org/10.1016/S0021-9258(19)41605-0>
  • FRIC Ivo, FLEGEL Martin, ZAORAL Milan, KODICEK Milan: Circular-Dichroic Spectra of Vasopressin Analogues and Their Cyclic Fragments. Eur J Biochem 1975, 56, 493. <https://doi.org/10.1111/j.1432-1033.1975.tb02255.x>
  • Krejčí Ivan, Barth Tomislav, Kupková Běla, Fruhaufová Linda, Flegel Martin, Zaoral Milan: Pharmacology of oxytocin-(1 -6)-hexapeptide amide, vasopressin-(1 -6)-hexapeptide amide and their deamino analogues. European Journal of Pharmacology 1973, 24, 179. <https://doi.org/10.1016/0014-2999(73)90069-1>
  • Brewster A. I. Richard, Hruby V. J., Glasel J. A., Tonelli A. E.: Proposed conformations of oxytocin and selected analogs in dimethyl sulfoxide as deduced from proton magnetic resonance studies. Biochemistry 1973, 12, 5294. <https://doi.org/10.1021/bi00750a012>
  • ZAORAL M., FLEGEL M.: ChemInform Abstract: AMINOSAEUREN UND PEPTIDE 106. MITT. SYNTH. UND BIOLOGISCHE EIGENSCHAFTEN DES CYCLISCHEN TEILS DES VASOPRESSIN‐ UND OXYTOCIN‐MOLEKUELS. Chemischer Informationsdienst 1972, 3. <https://doi.org/10.1002/chin.197234432>