McGuigan C.
40
Coauthors
6
Documentos
Volumen de publicaciones por año
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| Año de publicación | Num. Publicaciones |
|---|---|
| 1996 | 2 |
| 1997 | 1 |
| 1998 | 2 |
| 1999 | 1 |
Publicaciones por áreas de conocimiento
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| Área de conocimiento | Num. Publicaciones |
|---|---|
| Farmacología | 12 |
| Bioquímica | 2 |
| Descubrimiento de fármacos | 1 |
| Infección | 1 |
Publicaciones por áreas temáticas
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| Área temática | Num. Publicaciones |
|---|---|
| Farmacología y terapéutica | 5 |
| Enfermedades | 4 |
| Bioquímica | 3 |
| Fisiología humana | 1 |
| Cristalografía | 1 |
| Química orgánica | 1 |
Principales fuentes de datos
| Origen | Num. Publicaciones |
|---|---|
| Scopus | 6 |
| Google Scholar | 0 |
| RRAAE | 0 |
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Coautores destacados por número de publicaciones
| Coautor | Num. Publicaciones |
|---|---|
| De Clercq E. | 6 |
| Antonio Salgado | 6 |
| Cahard D. | 5 |
| Balzarini J. | 4 |
| Naesens L. | 3 |
| Velázquez S. | 3 |
| Yarnold C.J. | 2 |
| Bidois L. | 2 |
| Pathirana R. | 1 |
| Saboulard D. | 1 |
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Top Keywords
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Publicaciones del autor
Phosphoramidates as potent prodrugs of anti-HIV nucleotides: Studies in the amino region
ArticleAbstract: Novel phosphoramidate derivatives of the anti-HIV nucleoside analogues AZT and d4T have been preparePalabras claves:AZT, d4T, hiv, Nucleotide, ProdrugAutores:Antonio Salgado, Baizarinl J., Cahard D., De Clercq E., McGuigan C.Fuentes:scopusNovel nucleoside phosphoramidates as inhibitors of HIV: Studies on the stereochemical requirements of the phosphoramidate amino acid
ArticleAbstract: Novel phosphoramidate derivatives of the anti-HIV nucleoside analogue d4T were designed to act as laPalabras claves:d4T, hiv, Nucleotide, Phosphoramidate, Prodrug, Reverse transcriptaseAutores:Antonio Salgado, Balzarini J., De Clercq E., Harries T.Y., McGuigan C., Yarnold C.J.Fuentes:scopusMetabolism and anti-HIV activity of phosphoramidate derivatives of D4T-MP with variations in the amino acid moiety
ArticleAbstract: The metabolism of different phosphoramidate prodrugs of d4T-MP, in which the phosphate group is linkPalabras claves:Autores:Antonio Salgado, Baizarini J., Bidois L., Cahard D., De Clercq E., McGuigan C., Naesens L.Fuentes:scopusCharacterization of the activation pathway of phosphoramidate triester prodrugs of stavudine and zidovudine
ArticleAbstract: The phosphoramidate triester prodrugs of anti-human HIV 2',3'- dideoxynucleoside analogs (ddN) reprePalabras claves:Autores:Antonio Salgado, Balzarini J., Cahard D., De Clercq E., McGuigan C., Naesens L., Pathirana R., Saboulard D., Velázquez S.Fuentes:scopusMarked inhibitory activity of masked aryloxy aminoacyl phosphoramidate derivatives of dideoxynucleoside analogues against visna virus infection
ArticleAbstract: Lipophilic masked aryloxyaminoacylphosphoramidate derivatives of 2',3'- dideoxynucleoside (ddN) analPalabras claves:(Dideoxy)nucleoside analogues, AIDs, hiv, Masked aryloxyaminoacylphosphoramidate (dideoxy)nucleoside analogues, Reverse transcriptase, Visna virusAutores:Antonio Salgado, Balzarini J., Cahard D., De Clercq E., McGuigan C., Thormar H., Velázquez S., Wedgwood O., Yarnold C.J.Fuentes:scopus