Evidence of a peptide backbone contribution toward selective receptor recognition for leucine enkephalin thioamide analogs-Reference-Cited by-同舟云学术

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Evidence of a peptide backbone contribution toward selective receptor recognition for leucine enkephalin thioamide analogs

Published:1984-04 Issue:1 Volume:120 Page:305-310
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Clausen Kim,Spatola Arno F.,Lemieux Carole,Schiller Peter W.,Lawesson Sven-Olov

Funder

Natur og Univers, Det Frie Forskningsråd

Heart And Stroke Foundation Of Quebec

National Institutes of Health

Medical Research Council Canada

North Atlantic Treaty Organization

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference20 articles.

1. Thioasparagine and derivatives for peptide synthesis. A trifluoroacetic acid catalyzed anisyl transfer to sulfur

2. Amino acids surrogates: an indirect method for the synthesis of peptides containing the thioasparaginyl residue

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1. Hydrogen Bond and Geometry Effects of Thioamide Backbone Modifications;The Journal of Organic Chemistry;2021-12-01

2. Recent Advances in Ynamide Coupling Reagent;Chinese Journal of Organic Chemistry;2021

3. Receptor selectivity from minimal backbone modification of a polypeptide agonist;Proceedings of the National Academy of Sciences;2018-11-15

4. Increasing the bioactive space of peptide macrocycles by thioamide substitution;Chemical Science;2018

5. Theoretical conformational analysis of opiate peptides Leu-Enkephalin (H-Tyr-Gly-Gly-Phe-Leu-OH) and its two thioamide analogs (H-Tyr-Glyψ[CSNH]Gly-Phe-Leu-OH) and (H-Tyr-Gly-Glyψ[CSNH]Phe-Leu-OH);Structural Chemistry;2017-11-04

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