F. G. de las Heras

发表

Nitric oxide-producing CD11b(+)Ly-6G(Gr-1)(+)CD31(ER-MP12)(+) cells in the spleen of cyclophosphamide-treated mice: implications for T-cell responses in immunosuppressed mice.

J. Garcia-Bustos, M. Fresno, M. Muñoz-Fernández, 2000, Blood.

Antiviral activity of uridine 5'-diphosphate glucose analogues against some enveloped viruses in cell culture.

F. G. de las Heras, G. Gil-Fernández, S. Pérez, 1987, Antiviral research.

Candida albicans infection enhances immunosuppression induced by cyclophosphamide by selective priming of suppressive myeloid progenitors for NO production.

M. Fresno, M. Muñoz-Fernández, M. Jiménez-Díaz, 2002, Cellular immunology.

Antifungal sordarins. part 3: synthesis and structure-activity relationships of 2',3'-fused oxirane derivatives.

J. Cuevas, J. Ruiz, Julia Castro, 2002, Bioorganic & medicinal chemistry letters.

Sordarins: In Vitro Activities of New Antifungal Derivatives against Pathogenic Yeasts, Pneumocystis carinii, and Filamentous Fungi

M. J. Almela, E. Herreros, D. Gargallo‐Viola, 1998, Antimicrobial Agents and Chemotherapy.

Synthesis of N-(2-acetamido-2,3-dideoxy-D-glucopyranos-3-yl)glycyl-L-alanyl-D -isoglutamine analogues of muramyl dipeptide.

F. G. de las Heras, A. Calvo-Mateo, 1986, Carbohydrate research.

Nucleosides. XCIV. Synthesis of some C nucleosides by 1,3-dipolar cycloadditions to 3-(ribofuranosyl) propiolates.

R. Klein, S. Tam, F. G. de las Heras, 1976, The Journal of organic chemistry.

Activities of Sordarins in Murine Histoplasmosis

J. Graybill, A. Fothergill, L. Najvar, 1999, Antimicrobial Agents and Chemotherapy.

Antifungal Activities of Two New Azasordarins, GW471552 and GW471558, in Experimental Models of Oral and Vulvovaginal Candidiasis in Immunosuppressed Rats

J. Regadera, S. Ferrer, Inmaculada Santos, 2001, Antimicrobial Agents and Chemotherapy.

Identification and Activity of a Series of Azole-based Compounds with Lactate Dehydrogenase-directed Anti-malarial Activity*

Araceli, V. J. Winter, S. Croft, 2004, Journal of Biological Chemistry.

Alkylating nucleosides 1. Synthesis and cytostatic activity of N-glycosyl(halomethyl)-1,2,3-triazoles. A new type of alkylating agent.

F. G. de las Heras, G. Alonso, R. Alonso, 1979, Journal of medicinal chemistry.

Synthesis and antiviral activity of 3'-C-cyano-3'-deoxynucleosides.

E. De Clercq, Á. Díaz‐Ortiz, J. Balzarini, 1989, Journal of Medicinal Chemistry.

Mode of action of a new type of UDP-glucose analog against herpesvirus replication

Luis Carrasco, M. García-López, F. G. de las Heras, 1988, Antimicrobial Agents and Chemotherapy.

Selective benzoylation of 2-deoxy-D-arabino-hexose: synthesis of 3,6-di-O-benzoyl-2,4-dideoxy-D-threo-hexopyranose.

F. G. de las Heras, J. Fiandor, 1986, Carbohydrate research.

Uridine 5'-diphosphate glucose analogues. Inhibitors of protein glycosylation that show antiviral activity.

Luis Carrasco, M. García-López, M. Camarasa, 1985, Journal of medicinal chemistry.

Plasmodium falciparum: stage specific effects of a selective inhibitor of lactate dehydrogenase.

S. Croft, J. Lavandera, David Barros, 2005, Experimental parasitology.

Synthesis and antiviral evaluation of nucleosides of 5-methylimidazole-4-carboxamide.

Luis Carrasco, M. García-López, J. Andrés, 1985, Journal of Medicinal Chemistry.