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Non-nucleoside reverse transcriptase inhibitors (Part 18): synthesis and anti-HIV activity of 4-allylamino or 4-azido substituted diaryltriazines / 药学学报
Acta Pharmaceutica Sinica ; (12): 145-149, 2009.
Artículo en Inglés | WPRIM | ID: wpr-232582
ABSTRACT
Eight new diaryltriazine derivatives containing 4-allylamino and 4-azido substitutes guided by molecular docking have been designed and synthesized based on our previous work. The evaluation of HIV inhibitory activity demonstrated that all compounds were potent against HIV-1 replication. The most active compound 7c exhibited activity against HIV-1 (IC50 = 0.034 micromol x L(-1), SI = 6,475) and the double mutant strain (IC50 = 9.39 micromol x L(-1)) in the micromolar range, which was more potent than nevirapine.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Triazinas / Estructura Molecular / Química / VIH-1 / Inhibidores de la Transcriptasa Inversa / Fármacos Anti-VIH / Concentración 50 Inhibidora / Dominio Catalítico Idioma: Inglés Revista: Acta Pharmaceutica Sinica Año: 2009 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Triazinas / Estructura Molecular / Química / VIH-1 / Inhibidores de la Transcriptasa Inversa / Fármacos Anti-VIH / Concentración 50 Inhibidora / Dominio Catalítico Idioma: Inglés Revista: Acta Pharmaceutica Sinica Año: 2009 Tipo del documento: Artículo