Search Results - "BELLEVERGUE, P" :: K.UTB vyhledávací portál

The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C

by TOULEC, D, PIANETTI, P, DUHAMEL, L, CHARON, D, KIRILOVSKY, J, COSTE, H, BELLEVERGUE, P, GRAND-PERRET, T, AJAKANE, M, BAUDET, V, BOISIN, P, BOURSIER, E, LORIOLLE, F
Published in The Journal of biological chemistry (25.08.1991)

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Alkyl Hydrogen Phosphonate Derivatives of the anti-HIV Agent AZT may be Less Toxic than the Parent Nucleoside Analogue

by McGuigan, C., Bellevergue, P., Jones, B. C. N. M., Mahmood, N., Hay, A. J., Petrik, J., Karpas, A.
Published in Antiviral chemistry & chemotherapy (01.08.1994)

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Alkyl hydrogen phosphonate derivatives of the anti-HIV agent AZT may be less toxic than the parent nucleoside analogue

by MCGUIGAN, C, BELLEVERGUE, P, JONES, B. C. N. M, MAHMOOD, N, HAY, A. J, PETRIK, J, KARPAS, A
Published in Antiviral chemistry & chemotherapy (1994)

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Certain phosphoramidate derivatives of dideoxy uridine (ddU) are active against HIV and successfully by-pass thymidine kinase

by McGuigan, Christopher, Bellevergue, Patrice, Sheeka, Hendrika, Mahmood, Naheed, Hay, Alan J.
Published in FEBS letters (29.08.1994)

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6[(aryl and heteroaryl)oxy] methyl] naphthalene-2-carboximidamide derivatives, preparation and therapeutic application thereof

by P. BELLEVERGUE, C. ALCOUFFE, G. DELLAC
Year of Publication 17.07.2002

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Patent

The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C

Alkyl Hydrogen Phosphonate Derivatives of the anti-HIV Agent AZT may be Less Toxic than the Parent Nucleoside Analogue

Alkyl hydrogen phosphonate derivatives of the anti-HIV agent AZT may be less toxic than the parent nucleoside analogue

Certain phosphoramidate derivatives of dideoxy uridine (ddU) are active against HIV and successfully by-pass thymidine kinase

6[(aryl and heteroaryl)oxy] methyl] naphthalene-2-carboximidamide derivatives, preparation and therapeutic application thereof

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