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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| Formato: | Capítulo de libro |
| Lenguaje: | Inglés |
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2005
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| Acceso en línea: | Registro en Scopus Handle Registro en la Biblioteca Digital |
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| LEADER | 04478caa a22007217a 4500 | ||
|---|---|---|---|
| 001 | PAPER-22079 | ||
| 003 | AR-BaUEN | ||
| 005 | 20230518205336.0 | ||
| 008 | 190411s2005 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-22244435904 | |
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 030 | |a JHTCA | ||
| 100 | 1 | |a Martins Alho, M.A. | |
| 245 | 1 | 0 | |a Synthesis and antiviral evaluation of some carbonucleoside analogues |
| 260 | |c 2005 | ||
| 270 | 1 | 0 | |m CIHIDECAR (CONICET), Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales ArgentinaArgentina; email: norma@qo.fcen.uba.ar |
| 506 | |2 openaire |e Política editorial | ||
| 504 | |a Zhang, H.Y., Yu, H.W., Ma, L.T., Min, J.M., Zhang, L.H., (1998) Tetrahedron Asymmetry, 9, p. 141 | ||
| 504 | |a Yu, H.W., Zhang, H.Y., Yang, Z.J., Min, J.M., Ma, L.T., Zhang, L.H., (1998) Pure Appl. Chem., 70, p. 435 | ||
| 504 | |a Yang, Z.J., Yu, H.W., Min, J.M., Ma, L.T., Zhang, L.H., (1997) Tetrahedron Asymmetry, 8, p. 2739 | ||
| 504 | |a Zhang, M., Zhang, H., Yang, Z., Ma, L., Min, J., Zhang, L., (1999) Carbohydr. Res., 318, p. 157 | ||
| 504 | |a Lehman, J., Steck, J., Weiser, W., (1998) Carbohydr. Res., 184, p. 113 | ||
| 504 | |a Lehman, J., Sandhoff, K., (1990) Justus Liebigs Ann. Chem., p. 1261 | ||
| 504 | |a Casiraghi, G., Cornia, M., Rassu, G., Sante, C.D., Spanu, P., (1992) Tetrahedron, 48, p. 5619 | ||
| 504 | |a Damonte, E.B., Junin virus (2002) Wiley Encyclopedia of Molecular Medicine, pp. 1844-1846. , Creighton, T. E., Eds.; John Wiley & Sons, New York | ||
| 504 | |a Martins Alho, M.A., D'Accorso, N.B., (2000) J. Heterocyclic Chem., 37, p. 811 | ||
| 504 | |a Seldes, A.M., D'Accorso, N.B., Souto, M.F., Martins Alho, M., Arabehety, C., (2001) J. Mass Spectrom., 36, p. 1069 | ||
| 504 | |a Martins Alho, M.A., D'Accorso, N.B., (1999) J. Heterocyclic Chem., 36, p. 177 | ||
| 504 | |a McKee, K.T., Huggins, J.W., Trahan, C.J., Mahlandi, B.G., (1988) Antimicrob. Agents Chemother., 32, p. 1304 | ||
| 504 | |a Enria, D.A., Maiztegui, J.I., (1994) Antiviral Res., 23, p. 23 | ||
| 504 | |a Fascio, M.L., Montesano, V.J., D'Accorso, N.B., (1998) J. Heterocyclic Chem., 35, p. 103. , and references therein | ||
| 520 | 3 | |a 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. |l eng | |
| 593 | |a CIHIDECAR (CONICET), Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales Argentina, Argentina | ||
| 593 | |a Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales Argentina, Argentina | ||
| 690 | 1 | 0 | |a 1,2 O ISOPROPYLIDENE ALPHA DEXTRO XYLOPENTADIALDO 1,4 FURANOSE |
| 690 | 1 | 0 | |a 1,2 O ISOPROPYLIDENE ALPHA LEVO FURANOSYL DERIVATIVE |
| 690 | 1 | 0 | |a ANTIVIRUS AGENT |
| 690 | 1 | 0 | |a CARBONUCLEOSIDE DERIVATIVE |
| 690 | 1 | 0 | |a HETEROCYCLIC COMPOUND |
| 690 | 1 | 0 | |a NUCLEOSIDE DERIVATIVE |
| 690 | 1 | 0 | |a PYRANOSYL DERIVATIVE |
| 690 | 1 | 0 | |a UNCLASSIFIED DRUG |
| 690 | 1 | 0 | |a ANTIVIRAL ACTIVITY |
| 690 | 1 | 0 | |a ARTICLE |
| 690 | 1 | 0 | |a DENGUE VIRUS |
| 690 | 1 | 0 | |a DRUG SYNTHESIS |
| 690 | 1 | 0 | |a HERPES SIMPLEX VIRUS 1 |
| 690 | 1 | 0 | |a JUNIN VIRUS |
| 690 | 1 | 0 | |a NONHUMAN |
| 700 | 1 | |a Errea, M.I. | |
| 700 | 1 | |a Sguerra, V.L. | |
| 700 | 1 | |a D'Accorso, N.B. | |
| 700 | 1 | |a Talarico, L.B. | |
| 700 | 1 | |a García, C.C. | |
| 700 | 1 | |a Damonte, E.B. | |
| 773 | 0 | |d 2005 |g v. 42 |h pp. 979-983 |k n. 5 |p J. Heterocycl. Chem. |x 0022152X |w (AR-BaUEN)CENRE-780 |t Journal of Heterocyclic Chemistry | |
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| 856 | 4 | 0 | |u https://hdl.handle.net/20.500.12110/paper_0022152X_v42_n5_p979_MartinsAlho |y Handle |
| 856 | 4 | 0 | |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v42_n5_p979_MartinsAlho |y Registro en la Biblioteca Digital |
| 961 | |a paper_0022152X_v42_n5_p979_MartinsAlho |b paper |c PE | ||
| 962 | |a info:eu-repo/semantics/article |a info:ar-repo/semantics/artículo |b info:eu-repo/semantics/publishedVersion | ||
| 963 | |a VARI | ||
| 999 | |c 83032 | ||