Synthesis of blood serum thymic factor and its analogs

1986 ◽  
Vol 51 (12) ◽  
pp. 2909-2918 ◽  
Author(s):  
Martin Černý ◽  
Evžen Kasafírek ◽  
Jozef Rovenský ◽  
Jiří Křepelka

The blood serum thymic factor (FTS) and its two analogs (desGlp1)-FTS and (Gln1)-FTS were synthesized by a novel procedure. The biological activity of these compounds was assayed by the E-rosette test. The activity of (desGlp1)-FTS is decreased and (Gln1)-FTS shows an inhibitory effect.

2009 ◽  
Vol 21 (2) ◽  
pp. 135-144 ◽  
Author(s):  
JUNICHIRO GYOTOKU ◽  
AKIRA IMAIZUMI ◽  
SHIGEYUKI TERADA ◽  
EIJI KIMOTO

FEBS Letters ◽  
1981 ◽  
Vol 128 (1) ◽  
pp. 108-110 ◽  
Author(s):  
Akira Imaizumi ◽  
Junichiro Gyotoku ◽  
Shigeyuki Terada ◽  
Eiji Kimoto

1982 ◽  
Vol 79 (17) ◽  
pp. 5370-5373 ◽  
Author(s):  
M. Dardenne ◽  
J. M. Pleau ◽  
B. Nabarra ◽  
P. Lefrancier ◽  
M. Derrien ◽  
...  

1982 ◽  
Vol 4 (4) ◽  
pp. 298
Author(s):  
M. Dardenne ◽  
J.M. Pléau ◽  
B. Nabarra ◽  
P. Lefrancier ◽  
M. Derrien ◽  
...  

ChemInform ◽  
1987 ◽  
Vol 18 (18) ◽  
Author(s):  
M. CERNY ◽  
E. KASAFIREK ◽  
J. ROVENSKY ◽  
J. KREPELKA

2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Amal Thebti ◽  
M. A. K. Sanhoury ◽  
H-I. Ouzari ◽  
T. Barhoumi-slimi

The synthesis of new substituted arylphosphoramidates is performed in two steps through phosphorylation of the corresponding alcohols followed by aminolysis. The formation of the desired phosphoramidates depends on the subsequent addition of the two alcohols with the amine being added at the last step. The products were obtained in 58–95% yields. They were characterized mainly by multinuclear (1H, 13C, 31P, and 19F) NMR and IR spectroscopy. In addition, the antimicrobial and antiacetylcholinesterase activities were evaluated. The results showed acetylcholinesterase activity by some compounds, whilst no significant inhibitory effect against the tested bacterial strains has been recorded.


Author(s):  
L.N. GASTINEL ◽  
M. DARDENNE ◽  
J.M. PLEAU ◽  
J.F. BACH

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