Several 5-aminouracil derivatives that have previously been shown to inhibit Mycobacterium tuberculosis growth at concentrations of 5-40 μg/mL are demonstrated to act also as noncompetitive non-nucleoside inhibitors of HIV-1 reverse transcriptase without causing toxicity in vitro (McyrillicT-4 cells) and ex vivo (human tonsillar tissue).

5-arylaminouracil derivatives as potential dual-action agents

CORONA, ANGELA;TRAMONTANO, ENZO;
2015-01-01

Abstract

Several 5-aminouracil derivatives that have previously been shown to inhibit Mycobacterium tuberculosis growth at concentrations of 5-40 μg/mL are demonstrated to act also as noncompetitive non-nucleoside inhibitors of HIV-1 reverse transcriptase without causing toxicity in vitro (McyrillicT-4 cells) and ex vivo (human tonsillar tissue).
2015
5'-norcarbocyclic nucleoside analogs, 5-(phenylamino)uracil derivatives, Dual action, HIV and Mycobacterium tuberculosis co-infection, Biochemistry, Biotechnology, Molecular biology, Molecular medicine; Virology
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/175741
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