Synthesis and antiviral evaluation of some carbonucleoside analogues

1,2-O-Isopropylidene-α-L-threofuranosyl heterocyclic derivatives were synthesized from 1,2-O-isopropylidene-α-D-xilopentadialdo-1,4-furanose and tested for antiviral activity against herpes simplex virus type 1, dengue virus type 2 and Junín virus. For comparative propose, the antiviral activity of...

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Publicado: 2005
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v42_n5_p979_MartinsAlho
http://hdl.handle.net/20.500.12110/paper_0022152X_v42_n5_p979_MartinsAlho
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id paper:paper_0022152X_v42_n5_p979_MartinsAlho
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spelling paper:paper_0022152X_v42_n5_p979_MartinsAlho2023-06-08T14:46:50Z Synthesis and antiviral evaluation of some carbonucleoside analogues 1,2 o isopropylidene alpha dextro xylopentadialdo 1,4 furanose 1,2 o isopropylidene alpha levo furanosyl derivative antivirus agent carbonucleoside derivative heterocyclic compound nucleoside derivative pyranosyl derivative unclassified drug antiviral activity article Dengue virus drug synthesis Herpes simplex virus 1 Junin virus nonhuman 1,2-O-Isopropylidene-α-L-threofuranosyl heterocyclic derivatives were synthesized from 1,2-O-isopropylidene-α-D-xilopentadialdo-1,4-furanose and tested for antiviral activity against herpes simplex virus type 1, dengue virus type 2 and Junín virus. For comparative propose, the antiviral activity of some of their pyranosyl analogues were also tested. The furanosyl derivatives showed to be moderate inhibitors of Junin virus and, in general, proved to be more effective than the pyranosyl analogues. 2005 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v42_n5_p979_MartinsAlho http://hdl.handle.net/20.500.12110/paper_0022152X_v42_n5_p979_MartinsAlho
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 1,2 o isopropylidene alpha dextro xylopentadialdo 1,4 furanose
1,2 o isopropylidene alpha levo furanosyl derivative
antivirus agent
carbonucleoside derivative
heterocyclic compound
nucleoside derivative
pyranosyl derivative
unclassified drug
antiviral activity
article
Dengue virus
drug synthesis
Herpes simplex virus 1
Junin virus
nonhuman
spellingShingle 1,2 o isopropylidene alpha dextro xylopentadialdo 1,4 furanose
1,2 o isopropylidene alpha levo furanosyl derivative
antivirus agent
carbonucleoside derivative
heterocyclic compound
nucleoside derivative
pyranosyl derivative
unclassified drug
antiviral activity
article
Dengue virus
drug synthesis
Herpes simplex virus 1
Junin virus
nonhuman
Synthesis and antiviral evaluation of some carbonucleoside analogues
topic_facet 1,2 o isopropylidene alpha dextro xylopentadialdo 1,4 furanose
1,2 o isopropylidene alpha levo furanosyl derivative
antivirus agent
carbonucleoside derivative
heterocyclic compound
nucleoside derivative
pyranosyl derivative
unclassified drug
antiviral activity
article
Dengue virus
drug synthesis
Herpes simplex virus 1
Junin virus
nonhuman
description 1,2-O-Isopropylidene-α-L-threofuranosyl heterocyclic derivatives were synthesized from 1,2-O-isopropylidene-α-D-xilopentadialdo-1,4-furanose and tested for antiviral activity against herpes simplex virus type 1, dengue virus type 2 and Junín virus. For comparative propose, the antiviral activity of some of their pyranosyl analogues were also tested. The furanosyl derivatives showed to be moderate inhibitors of Junin virus and, in general, proved to be more effective than the pyranosyl analogues.
title Synthesis and antiviral evaluation of some carbonucleoside analogues
title_short Synthesis and antiviral evaluation of some carbonucleoside analogues
title_full Synthesis and antiviral evaluation of some carbonucleoside analogues
title_fullStr Synthesis and antiviral evaluation of some carbonucleoside analogues
title_full_unstemmed Synthesis and antiviral evaluation of some carbonucleoside analogues
title_sort synthesis and antiviral evaluation of some carbonucleoside analogues
publishDate 2005
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v42_n5_p979_MartinsAlho
http://hdl.handle.net/20.500.12110/paper_0022152X_v42_n5_p979_MartinsAlho
_version_ 1768543787202641920