scholarly journals Synthesis of Cyclic and Acyclic Pyrimidine Nucleosides Analogues with Anticipated Antiviral Activity

2018 ◽  
pp. 401-406
Author(s):  
Mohamed F. El-Shehry ◽  
Emad M. El Telbani ◽  
Mohamed I. Hegab
1969 ◽  
Vol 25 (1) ◽  
pp. 98-100 ◽  
Author(s):  
A. R. Diwan ◽  
R. K. Robins ◽  
W. H. Prusoff

ChemInform ◽  
1989 ◽  
Vol 20 (49) ◽  
Author(s):  
P. K. GUPTA ◽  
M. R. NASSIRI ◽  
L. A. COLEMAN ◽  
L. L. WOTRING ◽  
J. C. DRACH ◽  
...  

1989 ◽  
Vol 322 (1) ◽  
pp. 11-15 ◽  
Author(s):  
Julia Castro-Pichel ◽  
M. Teresa García-López ◽  
Federico G. de Las Heras ◽  
Rosario Herranz ◽  
Concepción Pérez ◽  
...  

2005 ◽  
Vol 24 (2) ◽  
pp. 153-160 ◽  
Author(s):  
Chang-Hyun Oh ◽  
Tae-Rim Baek ◽  
Joon Hee Hong

2018 ◽  
Vol 3 (8) ◽  
pp. 2321-2325 ◽  
Author(s):  
Liubov I. Kozlovskaya ◽  
Anastasia D. Golinets ◽  
Anastasia A. Eletskaya ◽  
Alexey A. Orlov ◽  
Vladimir A. Palyulin ◽  
...  

1995 ◽  
Vol 6 (6) ◽  
pp. 371-378 ◽  
Author(s):  
D. Loakes ◽  
D. M. Brown ◽  
N. Mahmood ◽  
J. Balzarini ◽  
E. De Clercq

A number of pyrimidine nucleosides, which may show two hydrogen bonding modes, have been prepared and tested for antiviral activity against a series of viruses. Whilst none of the compounds described showed significant activity against human immunodeficiency virus (HIV), the bicyclic 2′-deoxynucleoside, [2], derived from the base 6H,8H-3,4-dihydropyrimido[4,5-c][1,2]oxazin-7-one, was shown to inhibit herpes simplex virus type 1 (HSV-1) at similar concentrations as BVDU1 and ACV. Compounds 13, 6-(2-deoxyribofuranosyl)-6H,8H-2-methyl-3,4-dihydropyrimido[4,5-c][1,2]oxazin-7-one, and 14, N4-hydroxy-5-(2-chloroethyl)-2′-deoxyuridine, were as active as ACV against varicella-zoster virus (VZV).


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