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A Solid-phase Synthesis of [lysine]-vasopressin Through a Crystalline Protected Nonapeptide Intermediate

Overview
Journal J Am Chem Soc
Publisher American Chemical Society
Specialty Chemistry
Date 1968 May 22
PMID 5648114
Citations 8
Authors
J Meienhofer
Y Sano
Affiliations
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Citing Articles

Arginine-vasopressin, lysine-vasopressin, and oxytocin, C14-labeled in the glycine residue.

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Regulation of formation and proposed structure of the factor inhibiting the release of melanocyte-stimulating hormone.

Celis M, Taleisnik S, Walter R Proc Natl Acad Sci U S A. 1971; 68(7):1428-33.

PMID: 5283931 PMC: 389210. DOI: 10.1073/pnas.68.7.1428.

Solid-phase synthesis with attachment of peptide to resin through an amino acid side chain: (8-lysine)-vasopressin.

Meienhofer J, Trzeciak A Proc Natl Acad Sci U S A. 1971; 68(5):1006-9.

PMID: 5280519 PMC: 389101. DOI: 10.1073/pnas.68.5.1006.

Solid-phase synthesis of lysine vasopressin analogs: (1-beta-mercaptopropionic acid, 8-lysine)-vasopression and (1-beta-mercaptopropionic acid, 8-(epsilon-N-p-toluenesulfonyl)-lysine)-vasopressin.

Havran R Experientia. 1973; 29(5):520-1.

PMID: 4730272 DOI: 10.1007/BF01926638.

Conformation of lysine vasopressin: a comparison with oxytocin.

Walter R, Glickson J, SCHWARTZ I, Havran R, Meienhofer J, Urry D Proc Natl Acad Sci U S A. 1972; 69(7):1920-4.

PMID: 4505670 PMC: 426832. DOI: 10.1073/pnas.69.7.1920.