A PROTECTED ANGIOTENSIN II
- 1 June 1962
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 40 (6) , 1098-1102
- https://doi.org/10.1139/v62-167
Abstract
The preparation of an octapeptide, carbobenzoxy-(β-benzylester)-L-aspartyl-nitro-L-arginyl-L-valyl-L-tyrosyl-L-isoleucyl-(im)benzyl-L-histidyl-L-prolyl-L-phenylalanine methyl ester, a derivative of angiotensin II, is described.Keywords
This publication has 9 references indexed in Scilit:
- Preparation of Benzyl and p-Nitrobenzyl Esters of Amino Acids1The Journal of Organic Chemistry, 1961
- Studies on Polypeptides. XX. Synthesis and Corticotropic Activity of a Peptide Amide Corresponding to the N-Terminal Tridecapeptide Sequence of the Corticotropins1-4Journal of the American Chemical Society, 1961
- Syntheses of an Optically Pure Tetrapeptide Contained in Angiotensin1,2Journal of the American Chemical Society, 1959
- Synthese einer geschützten Pentapeptid‐Sequenz des Tyrocidins A unter Verwendung farbiger Schutzgruppen und des p‐Nitrobenzyl‐RestesHelvetica Chimica Acta, 1959
- CONTRIBUTED ARTICLESAnalytical Chemistry, 1958
- Synthèse d'analogues structuraux de l'oxytocineHelvetica Chimica Acta, 1956
- A New Method of Forming Peptide BondsJournal of the American Chemical Society, 1955
- Über aktivierte Ester. II. Synthese aktivierter Ester von Aminosäure‐DerivatenHelvetica Chimica Acta, 1955
- The Synthesis and Spectrophotometric Study of Poly-L-tyrosine and Poly-3,5-diiodotyrosine1Journal of the American Chemical Society, 1953