Literature DB >> 4759570

Symmetrical disulfide bonds as S-protecting groups and their cleavage by dithiothreitol: synthesis of oxytocin with high biological activity.

S Hase, R Walter.   

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Year:  1973        PMID： 4759570     DOI： 10.1111/j.1399-3011.1973.tb03463.x

Source DB:  PubMed          Journal:  Int J Pept Protein Res        ISSN： 0367-8377


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  4 in total

1.  Contribution of the peptide backbone to the action of oxytocin analogs.

Authors:  O Hechter; T Kato; S H Nakagawa; F Yang; G Flouret
Journal:  Proc Natl Acad Sci U S A       Date:  1975-02       Impact factor: 11.205

2.  Long-range, pH-dependent effects on the carbon-13 nuclear magnetic resonance spectra of oxytocin.

Authors:  R Deslauriers; R Walter; I C Smith
Journal:  Proc Natl Acad Sci U S A       Date:  1974-02       Impact factor: 11.205

3.  Amide hydrogen exchange rates of peptides in H2O solution by 1H nuclear magnetic resonance transfer of solvent saturation method. Conformations of oxytocin and lysine vasopressin in aqueous solution.

Authors:  N R Krishna; D H Huang; J D Glickson; R Rowan; R Walter
Journal:  Biophys J       Date:  1979-06       Impact factor: 4.033

4.  Enzymes as reagents in peptide synthesis: enzymatic removal of amine protecting groups.

Authors:  C Meyers; J D Glass
Journal:  Proc Natl Acad Sci U S A       Date:  1975-06       Impact factor: 11.205
  4 in total

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