(R)-9-(2-phosphonylmethoxypropyl)-2,6-diaminopurine is a potent inhibitor of feline immunodeficiency virus infection — Thomas W. Vahlenkamp (1995) | RDL Network
(R)-9-(2-phosphonylmethoxypropyl)-2,6-diaminopurine is a potent inhibitor of feline immunodeficiency virus infection
Article 1995 en
Authors
TV
Thomas W. Vahlenkamp
AR
A. de Ronde
JB
Jan Balzarini
Abstract
1 min read
The antiviral efficacy of acyclic nucleoside phosphonates, including 9-(2-phosphonylmethoxyethyl)adenine (PMEA) and (R)-9-(2-phosphonylmethoxypropyl)-2,6-diaminopurine [(R)-PMPDAP] against feline immunodeficiency virus (FIV) infection was determined. (R)-PMPDAP showed the highest selectivity index (> 2,000) in vitro. Treatment of experimentally FIV-infected asymptomatic cats with PMEA or (R)-PMPDAP had no effect on the CD4+/CD8+ ratio. However, mean plasma viral RNA concentrations decreased significantly in the (R)-PMPDAP-treated cats. Our data show that, in comparison to PMEA, (R)-PMPDAP is a more potent and less toxic inhibitor of FIV replication both in vitro and in vivo.
Katrin Hartmann, M Kuffer, Jan Balzarini, Lieve Naesens, Michel Goldberg, Volker Erfle, Frank-Detlef Goebel, De Clercq Erik, Jindřich Jindřich, Antonı́n Holý, Norbert Bischofberger, W Kraft
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