Antiviral activity and cross-resistance profile of P-1946, a novel human immunodeficiency virus type 1 protease inhibitor

The HIV protease inhibitor P-1946 is a member of a novel family of l-Lysine derivatives. The compound is a specific HIV-1 protease inhibitor that has potent and selective in vitro antiviral activity (EC 50 152 nM) against a range of isolates resistant to commercially available protease inhibitors. T...

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Veröffentlicht in:Antiviral research 2006-06, Vol.70 (2), p.17-20
Hauptverfasser: Sévigny, G., Stranix, B., Tian, B., Dubois, A., Sauvé, G., Petropoulos, C., Lie, Y., Hellmann, N., Conway, B., Yelle, J.
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Sprache:eng
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Zusammenfassung:The HIV protease inhibitor P-1946 is a member of a novel family of l-Lysine derivatives. The compound is a specific HIV-1 protease inhibitor that has potent and selective in vitro antiviral activity (EC 50 152 nM) against a range of isolates resistant to commercially available protease inhibitors. The presence of at least four primary and four secondary drug resistance mutations is required to achieve greater than four-fold resistance to P-1946. P-1946's favorable resistance profile makes it a good lead for the development of new agents active against existing PI-resistant virus in treatment-experienced patient.
ISSN:0166-3542
1872-9096
DOI:10.1016/j.antiviral.2005.12.006