Conformational preferences and binding to neurophysins of oxytocin analogs with sarcosine or N-methylalanine in position 7
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1985.tb02188.x/fullpdf
Reference6 articles.
1. Synthesis and some pharmacological properties of oxytocin and vasopressin analogs with sarcosine or N-methyl-L-alanine in position 7
2. Interactions of oxytocin with bovine neurophysins I and II. Use of carbon-13 nuclear magnetic resonance and hormones specifically enriched with carbon-13 in the glycinamide-9 and half-cystine-1 positions
3. Torsion angles in the cystine bridge of oxytocin in aqueous solution. Measurements of circumjacent vicinal couplings between proton, carbon-13, and nitrogen-15
4. Utilisation de l'effet overhauser des mesures de relaxation en RMN 1H, et des deplacements chimiques en RMN 13C dans l'etude de la conformation des amides—I
5. Side chain conformations of oxytocin and vasopressin studied by NMR observation of isotopic isomers
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1. Revealing the Relationship between Electric Fields and the Conformation of Oxytocin Using Quasi-Static Amide-I Two-Dimensional Infrared Spectra;ACS Omega;2022-01-19
2. Design of Oxytocin Analogs;Methods in Molecular Biology;2019
3. New, Potent, and Selective Peptidic Oxytocin Receptor Agonists;Journal of Medicinal Chemistry;2014-06-12
4. In position 7 l- and d-Tic-substituted oxytocin and deamino oxytocin: NMR study and conformational insights;Amino Acids;2010-01-27
5. Conformational analysis of [Cpp1, Sar7, Arg8] vasopressin by 1H-NMR spectroscopy and molecular mechanics calculations;International Journal of Peptide and Protein Research;2009-01-12
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