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Structure-activity relationships in platelet-activating factor. 12. Synthesis and biological evaluation of platelet-activating factor antagonists with anti-HIV-1 activity.
Serradji, Nawal; Martin, Marc; Bensaid, Okkacha; Cisternino, Salvatore; Rousselle, Christophe; Dereuddre-Bosquet, Nathalie; Huet, Jack; Redeuilh, Catherine; Lamouri, Aazdine; Dong, Chang-Zhi; Clayette, Pascal; Scherrmann, Jean-Michel; Dormont, Dominique; Heymans, Françoise.
Afiliación
  • Serradji N; Unité de Recherche Pharmacochimie Moléculaire et Systèmes Membranaires, Laboratoire de Pharmacochimie Moléculaire, Université Paris 7-Denis Diderot, 2 Place Jussieu, 75251 Paris Cedex 05, France.
J Med Chem ; 47(25): 6410-9, 2004 Dec 02.
Article en En | MEDLINE | ID: mdl-15566310
The HIV-1 central nervous system infection leads to the onset of neurological impairments called AIDS dementia complex (ADC). PAF plays an important role in this pathology, as it is an HIV-1-induced neurotoxin produced by infected or activated macrophages and microglia, in the brain. We previously reported that PAF-antagonists bearing a trisubstituted piperazine presented in vitro anti-HIV-1 activity in human macrophages. To improve the pharmacological activities of our lead compound, 1a, we modified its carbamate function and evaluated both its antiretroviral and anti-PAF activities. One carbamate derivative (10c) demonstrated a similar antiviral activity but a higher anti-PAF potency, whereas 4a, with an ureide function, presents an increased antiviral activity and can be considered as a pure antiretroviral drug, as it does not present PAF-antagonism. Moreover, we measured the ability of 1a to cross the blood-brain barrier, using the in situ mouse brain perfusion method and its plasmatic concentrations after iv and po administration. The transport parameter measured (K(in)) proves that 1a is able to cross this biological barrier, but a pharmacokinetic study reveals its weak bioavailability in rats.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piperazinas / Factor de Activación Plaquetaria / VIH-1 / Fármacos Anti-VIH Límite: Animals / Humans / Male Idioma: En Revista: J Med Chem Asunto de la revista: QUIMICA Año: 2004 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piperazinas / Factor de Activación Plaquetaria / VIH-1 / Fármacos Anti-VIH Límite: Animals / Humans / Male Idioma: En Revista: J Med Chem Asunto de la revista: QUIMICA Año: 2004 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos