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Species-dependent enantioselective pharmacokinetics of PNU-103017, a Pyrone HIV protease inhibitor

โœ Scribed by Wei-Zhu Zhong; Marta G. Williams; Marie T. Borin; Guy E. Padbury


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
107 KB
Volume
10
Category
Article
ISSN
0899-0042

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โœฆ Synopsis


PNU-103017, 4-Cyano-N-(3-(cyclopropyl(5,6,7,8,9

,10-hexahydro-4hydroxy-2-oxo-2H-cycloocta(b) pyran-3-yl)methyl)phenyl)-benzenesulfonamide, is a selective HIV aspartyl protease inhibitor under evaluation as a potential oral treatment of Acquired Immunodeficiency Diseases. PNU-103017 is a racemic mixture of two enantiomers, designated PNU-103264 (R-) and PNU-103265 (S-). Stereoselective pharmacokinetics of the two enantiomers of PNU-103017 were observed in the dog, rat, and human after single and multiple dose administration of the racemate and were apparently species-dependent. Mean enantiomeric ratios of plasma concentrations (R-/S-) at each time point were greater than 1 in the dog, ranging from 1.22 to 3.06, but less than 1 in the rat and in the human, ranging from 0.44 to 0.80 and 0.23 to 0.73, respectively. A trend towards increased or decreased (farther from 1:1, R-/S-) enantiomeric ratio of plasma concentrations with time after each administration was also observed. The enantiomeric ratio remained unchanged after multiple dose administration in the rat, dog, and human although enzyme induction and increased plasma clearance were observed for both enantiomers.


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