Piperidinylethyl-, phenoxyethyl-, and .beta.-fluorophenethyl-substituted thiourea compounds with potent anti-HIV activity

   
   

The present invention is directed to derivatives of piperidinylethyl, phenoxyethyl, and fluorophenethyl bromopyridyl thioureas, which have been found to be effective non-nucleoside inhibitors (NNRTI) of NNI-resistant and multi-drug resistant human immunodeficiency virus (HIV)-1 reverse transcriptase (RT). The present invention is further directed to methods of using the above derivatives to treat patients with NNI-resistant or multi-drug resistant human immunodeficiency virus (HIV)-1.

Присытствыющий вымысел направлен к производным piperidinylethyl, phenoxyethyl, и thioureas bromopyridyl fluorophenethyl, которые были найдены, что будут эффективными иами АБС битор нон-nukleozida (NNRTI) вируса ННИ-upornyx и мулти-snadob64 упорного людского иммунодефицита (обратного transcriptase HIV)-1 (rt). Присытствыющий вымысел более добавочно направлен к методам использования вышеуказанных производных обработать пациентов с вирусом ННИ-upornyx или мулти-snadob64 упорным людским иммунодефицита (HIV)-1.

 
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