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Farmaco ; 52(12): 751-3, 1997 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9648281

RESUMO

We synthetized pyridobenzoxazocynone that differs in the enlarged eight-membered heterocyclic system from the basic structure of pyridobenzoxazepinones a known class of non-nucleoside HIV-1 reverse transcriptase inhibitors. Pyridobenzoxazocynone hydrochloride was found to inhibit HIV-1 reverse transcriptase activity. At concentration 0.35 microM the enzyme activity decreased by 64 +/- 14%. Higher concentrations of pyridobenzoxazocynone hydrochloride completely abolished the enzyme activity expressed as radioactivity of acid insoluble products. These results suggest that pyridobenzoxazocynones may represent a new class of HIV-1 reverse transcriptase inhibitors.


Assuntos
Transcriptase Reversa do HIV/antagonistas & inibidores , Oxazocinas/síntese química , Piridinas/síntese química , Inibidores da Transcriptase Reversa/síntese química , Produtos do Gene pol/antagonistas & inibidores , Humanos , Estrutura Molecular , Oxazocinas/farmacologia , Piridinas/farmacologia , Inibidores da Transcriptase Reversa/farmacologia
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