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1.
J Med Chem ; 52(1): 151-69, 2009 Jan 08.
Artículo en Inglés | MEDLINE | ID: mdl-19072656

RESUMEN

Dopamine D(3) antagonism combined with serotonin 5-HT(1A) and 5-HT(2A) receptor occupancy may represent a novel paradigm for developing innovative antipsychotics. The unique pharmacological features of 5i are a high affinity for dopamine D(3), serotonin 5-HT(1A) and 5-HT(2A) receptors, together with a low affinity for dopamine D(2) receptors (to minimize extrapyramidal side effects), serotonin 5-HT(2C) receptors (to reduce the risk of obesity under chronic treatment), and for hERG channels (to reduce incidence of torsade des pointes). Pharmacological and biochemical data, including specific c-fos expression in mesocorticolimbic areas, confirmed an atypical antipsychotic profile of 5i in vivo, characterized by the absence of catalepsy at antipsychotic dose.


Asunto(s)
Antipsicóticos/síntesis química , Antipsicóticos/farmacología , Conducta Animal/efectos de los fármacos , Diseño de Fármacos , Receptor de Serotonina 5-HT1A/metabolismo , Receptor de Serotonina 5-HT2A/metabolismo , Receptores de Dopamina D3/metabolismo , Animales , Antipsicóticos/química , Antipsicóticos/clasificación , Sitios de Unión , Evaluación Preclínica de Medicamentos , Humanos , Ligandos , Ratones , Modelos Moleculares , Estructura Molecular , Unión Proteica , Relación Estructura-Actividad
2.
Curr Pharm Des ; 8(8): 615-57, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-11945162

RESUMEN

Along with nucleoside reverse transcriptase inhibitors (NRTIs) and protease inhibitors (PIs), non-nucleoside reverse transcriptase inhibitors (NNRTIs) have gained a definitive and important place in the treatment of HIV-1 infections, and are in rapid development. These compounds can be grouped into two classes: the first generation NNRTIs, mainly discovered by random screening, and the second generation NNRTIs, developed as a result of comprehensive strategies involving molecular modelling, rationale-based drug synthesis, biological and pharmacokinetic evaluations. The recent boom of NNRTIs is mainly due to their antiviral potency, high specificity and low toxicity. The rapid emergence of drug-resistant HIV-1 strains induced by the first generation drugs is a disadvantage bypassed, in part, by the broad spectrum second generation NNRTIs. Starting from the first generation, this review will focus on the second generation NNRTIs dealing with the recent and most interesting published results, highlighting the guidelines for the development of a third generation of NNRTIs.


Asunto(s)
Fármacos Anti-VIH/química , Diseño de Fármacos , Transcriptasa Inversa del VIH/antagonistas & inhibidores , Inhibidores de la Transcriptasa Inversa/química , Timidina/análogos & derivados , Síndrome de Inmunodeficiencia Adquirida/tratamiento farmacológico , Alquinos , Fármacos Anti-VIH/uso terapéutico , Benzodiazepinonas/química , Benzodiazepinonas/uso terapéutico , Benzoxazinas , Ciclopropanos , Delavirdina/química , Delavirdina/uso terapéutico , Evaluación Preclínica de Medicamentos/tendencias , Farmacorresistencia Viral , Quimioterapia Combinada , VIH-1/efectos de los fármacos , Humanos , Estructura Molecular , Nevirapina/química , Nevirapina/uso terapéutico , Nucleósidos/química , Nucleósidos/uso terapéutico , Oxazinas/química , Oxazinas/uso terapéutico , Inhibidores de la Transcriptasa Inversa/uso terapéutico , Compuestos de Espiro/química , Compuestos de Espiro/uso terapéutico , Timidina/química , Timidina/uso terapéutico , Uridina/análogos & derivados
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