𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective disposition of hydroxychloroquine and its metabolites in rats

✍ Scribed by Yimin Wei; Gloria A. Nygard; Shari L. Ellertson; Shoukry K.W. Khalil


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
576 KB
Volume
7
Category
Article
ISSN
0899-0042

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Stereoselective disposition of ibuprofen
✍ Romualda D. Knihinicki; Richard O. Day; Garry G. Graham; Kenneth M. Williams πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 655 KB

R)-2-Arylpropionates are often inverted to the pharmacologically active S-enantiomers in vivo, although there is significant interspecies variability in inversion. In order to provide a basis for determining the biochemical consequences of this unique process using rats as a model, it was important

Stereoselective determination of hydroxy
✍ Anderson Rodrigo Moraes de Oliveira; Carmen Dickow Cardoso; Pierina Sueli Bonato πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 473 KB

## Abstract Liquid‐phase microextraction based on polypropylene hollow fibers and CE were applied for the chiral determination of hydroxychloroquine (HCQ) and its metabolites (desethylchloroquine, DCQ; desethylhydroxychloroquine, DHCQ; bisdesethylchloroquine, BDCQ) in human urine. The analytes were

Stereoselective disposition of tiaprofen
✍ K. Erb; R. Brugger; K. Williams; G. Geisslinger πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 100 KB πŸ‘ 2 views

The pharmacokinetics and metabolic chiral inversion of the S(+)-and R(-)-enantiomers of tiaprofenic acid (S -TIA, R-TIA) were assessed in vivo in rats, and in addition the biochemistry of inversion was investigated in vitro in rat liver homogenates. Drug enantiomer concentrations in plasma were inve