Collect. Czech. Chem. Commun.
1979, 44, 275-287
https://doi.org/10.1135/cccc19790275
Synthesis of oxytocin analogues modified in the tripeptide side-chain by condensation of aminoterminal linear hexapeptide with the carboxyterminal tripeptide
Jan Hlaváček, Tomislav Barth, Karel Bláha and Karel Jošt
Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6
Crossref Cited-by Linking
- ROY UMA, GAZIS DIANA, PAN G. DAL, SCHWARTZ I.L., ROY J.: Role of the carboxamide groups of the asparagine and glycinamide residues of oxytocin. Syntheses and biological properties of [5-β-cyanoalanine] oxytocin and [9-α-aminoacetonitrile] oxytocin. International Journal of Peptide and Protein Research 2009, 22, 525. <https://doi.org/10.1111/j.1399-3011.1983.tb02125.x>
- Budαěšínský M., Ragnarsson U., Lankiewicz L., Grehn L., Slaninová J., Hlaváček J.: Synthesis and utilization of 13C and 15N backbone-labeled proline: NMR study of synthesized oxytocin with backbone-labeled C-terminal tripeptide amide. Amino Acids 2005, 29, 151. <https://doi.org/10.1007/s00726-005-0183-z>
- Hlaváček Jan, Ragnarsson Ulf: Solid phase synthesis of partially protected tocinoic acid: Optimization with respect to resin and protecting groups. Journal of Peptide Science 2001, 7, 349. <https://doi.org/10.1002/psc.329>
- HLAVACEK J., BARTH T., BLAHA K., JOST K.: ChemInform Abstract: AMINO ACIDS AND PEPTIDES. CL. SYNTHESIS OF OXYTOCIN ANALOGS MODIFIED IN THE TRIPEPTIDE SIDE CHAIN BY CONDENSATION OF AMINOTERMINAL LINEAR HEXAPEPTIDE WITH THE CARBOXYTERMINAL TRIPEPTIDE. Chemischer Informationsdienst 1979, 10. <https://doi.org/10.1002/chin.197917381>
