N-acyl derivatives of organophosphorus analogs of amino acids, their esters, and amides

Author(s):  
N. B. Tarusova ◽  
I. A. Gandurina ◽  
Yu. N. Zhukov ◽  
G. M. Yakovleva ◽  
R. M. Khomutov
1980 ◽  
Vol 11 (15) ◽  
Author(s):  
N. B. TARUSOVA ◽  
I. A. GANDURINA ◽  
YU. N. ZHUKOV ◽  
G. M. YAKOVLEVA ◽  
R. M. KHOMUTOV

1980 ◽  
Vol 58 (7) ◽  
pp. 573-576 ◽  
Author(s):  
Alenka Paquet

Long-chain N-acyl derivatives of methionine, tryptophan, threonine, and lysine (N6) have been obtained by the reaction of succinimidyl esters of fatty acids with the unprotected amino acids. Their physical properties have been characterized.


Amino Acids ◽  
2004 ◽  
Vol 26 (2) ◽  
pp. 209-214 ◽  
Author(s):  
J. Wallach ◽  
F. Peypoux ◽  
O. Lapr�vote ◽  
M. Pagadoy

1987 ◽  
Vol 33 (7) ◽  
pp. 577-582 ◽  
Author(s):  
A. Paquet ◽  
K. Rayman

Several N-acyl derivatives of D-tryptophan, D-alanine, D-methionine, D-valine, and D-aspartic acid were synthesized in high yields using the succinimidyl ester method and examined for their antibotulinal properties. In conjunction with 60 ppm of sodium nitrite, sorbyl-D-tryptophan, sorbyl-D-alanine, myristoyl-D-aspartic acid, and glycyl-D-alanine were highly inhibitory. In the absence of sodium nitrite, the N-acyl derivatives of the D-amino acids were not inhibitory. On its own, 60 ppm of sodium nitrite was only slightly inhibitory. Sorbyl-L-tryptophan and sorbyl-L-alanine had no effect in the presence or absence of 60 ppm of sodium nitrite.


1984 ◽  
Vol 49 (11) ◽  
pp. 2557-2561 ◽  
Author(s):  
Václav Čeřovský ◽  
Karel Jošt

Phenylhydrazides of Nα-acyl derivatives of all coded amino acids, except proline, were prepared by papain (E.C. 3.4.22.2)-catalyzed synthesis. Comparison of yields affords information about the suitability of the amino acid in position P1 in papain-catalyzed syntheses of peptides.


FEBS Letters ◽  
1974 ◽  
Vol 40 (1) ◽  
pp. 207-209 ◽  
Author(s):  
A.A. Hochberg ◽  
D. Zevin-Sonkin ◽  
E. Ziv ◽  
N. de Groot ◽  
N. Lichtenstein

2003 ◽  
Vol 58 (5-6) ◽  
pp. 366-370 ◽  
Author(s):  
Nijole Dirvianskytė ◽  
Juozapas Straukas ◽  
Valdemaras Razumas ◽  
Eugenius Butkus

Abstract Synthesis of N- and O-acyl derivatives of ᴅʟ-serine and threo-ᴅʟ-phenylserine was accomplished by a regioselective acylation of the corresponding amino acid. The residues introduced into amino acid structure contain hydrophobic long chain or aromatic, namely lauroyl, myristoyl and phenylacetyl moieties. The fungicidal activity against six strains of fungi was studied. Several compounds were found to be effective against growth of fungi, and Omyristoyl- ᴅʟ-serine 2 and N-phenylacetyl-threo-ᴅʟ-phenylserine 8 completely inhibited the growth of the mycelium of the fungus Verticillium dahliae.


Sign in / Sign up

Export Citation Format

Share Document