Unusual Amino Acids Accessed Through Sugar?Amino Acid Hybrids and Incorporation into Biologically Active Peptides

ChemInform ◽  
2005 ◽  
Vol 36 (17) ◽  
Author(s):  
Frank Schweizer
1976 ◽  
Vol 29 (7) ◽  
pp. 1591 ◽  
Author(s):  
AP Hope ◽  
B Halpern

N-(2-Hydroxyarylmethy1ene)amino acids have been coupled with amino acid esters to form sterically pure N-protected dipeptide esters. The protecting group can be removed by means of 80% acetic acid under conditions which leaves the t-butyloxycarbonyl protecting group intact. Biologically active peptides which are C-terminal partial sequences of substance P were prepared and were shown to have the expected vasodilator, spasmogenic and venoconstrictor properties.


1960 ◽  
Vol 38 (4) ◽  
pp. 477-481 ◽  
Author(s):  
Saul B. Needleman ◽  
R. Quentin Blackwell ◽  
Leonard S. Fosdick

A group of biologically active peptides were examined for possible favored chain positions exhibited by some of the 21 constituent amino acids as well as for the unusual occurrence of specific peptide linkages. High levels of significance were revealed for certain amino acid couplets when they were subjected to chi-square analyses.


1998 ◽  
Vol 41 (14) ◽  
pp. 2481-2491 ◽  
Author(s):  
Maria Sandberg ◽  
Lennart Eriksson ◽  
Jörgen Jonsson ◽  
Michael Sjöström ◽  
Svante Wold

2016 ◽  
Vol 15 (5) ◽  
pp. 1487-1496 ◽  
Author(s):  
Johannes Koehbach ◽  
Christian W. Gruber ◽  
Christian Becker ◽  
David P. Kreil ◽  
Alexander Jilek

Peptides ◽  
2011 ◽  
Vol 32 (12) ◽  
pp. 2504-2510 ◽  
Author(s):  
Alberto Bryan ◽  
Leroy Joseph ◽  
James A. Bennett ◽  
Herbert I. Jacobson ◽  
Thomas T. Andersen

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