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Disposition and metabolic fate of atomoxetine hydrochloride: the role of CYP2D6 in human disposition and metabolism

Drug metabolism and disposition, 2003-01, Vol.31 (1), p.98

2003

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Pharmacological characterization of the competitive GLUK5 receptor antagonist decahydroisoquinoline LY466195 in vitro and in vivo

The Journal of pharmacology and experimental therapeutics, 2006-08, Vol.318 (2), p.772

2006

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Selective reduction of N-oxides to amines: application to drug metabolism

Drug metabolism and disposition, 2004-09, Vol.32 (9), p.966

2004

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Disposition and metabolic fate of atomoxetine hydrochloride: pharmacokinetics, metabolism, and excretion in the Fischer 344 rat and beagle dog

Drug metabolism and disposition, 2003-01, Vol.31 (1), p.88

2003

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The disposition, metabolism, and pharmacokinetics of a selective metabotropic glutamate receptor agonist in rats and dogs

Drug metabolism and disposition, 2002-01, Vol.30 (1), p.27

2002

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GluK1 antagonists from 6-(tetrazolyl)phenyl decahydroisoquinoline derivatives: In vitro profile and in vivo analgesic efficacy

Bioorganic & medicinal chemistry letters, 2013-12, Vol.23 (23), p.6463-6466

2013

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GluK1 antagonists from 6-(carboxy)phenyl decahydroisoquinoline derivatives. SAR and evaluation of a prodrug strategy for oral efficacy in pain models

Bioorganic & medicinal chemistry letters, 2013-12, Vol.23 (23), p.6459-6462

2013

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Biosynthesis of drug glucuronides for use as authentic standards

Journal of pharmacological and toxicological methods, 2002-05, Vol.47 (3), p.161-168

2002

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Two Prodrugs of Potent and Selective GluR5 Kainate Receptor Antagonists Actives in Three Animal Models of Pain

Journal of medicinal chemistry, 2005-06, Vol.48 (13), p.4200-4203

2005

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Determination of olanzapine in human breast milk by high-performance liquid chromatography with electrochemical detection

Journal of chromatography. B, Biomedical sciences and applications, 1999-04, Vol.726 (1), p.203-209

1999

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High Resolution Separation of Urinary Organic Acids by High Performance Liquid Chromatography

Journal of liquid chromatography, 1982-01, Vol.5 (12), p.2343-2357

1982

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Disposition and biotransformation of the antipsychotic agent olanzapine in humans

Drug metabolism and disposition, 1997-01, Vol.25 (1), p.81

1997

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Disposition and metabolic fate of atomoxetine hydrochloride: the role of CYP2D6 in human disposition and metabolism

Pharmacological characterization of the competitive GLUK5 receptor antagonist decahydroisoquinoline LY466195 in vitro and in vivo

Selective reduction of N-oxides to amines: application to drug metabolism

Disposition and metabolic fate of atomoxetine hydrochloride: pharmacokinetics, metabolism, and excretion in the Fischer 344 rat and beagle dog

The disposition, metabolism, and pharmacokinetics of a selective metabotropic glutamate receptor agonist in rats and dogs

GluK1 antagonists from 6-(tetrazolyl)phenyl decahydroisoquinoline derivatives: In vitro profile and in vivo analgesic efficacy

GluK1 antagonists from 6-(carboxy)phenyl decahydroisoquinoline derivatives. SAR and evaluation of a prodrug strategy for oral efficacy in pain models

Biosynthesis of drug glucuronides for use as authentic standards

Two Prodrugs of Potent and Selective GluR5 Kainate Receptor Antagonists Actives in Three Animal Models of Pain

Ethyl (3S,4aR,6S,8aR)-6-(4-Ethoxycar- bonylimidazol-1-ylmethyl)decahydroiso- quinoline-3-carboxylic Ester: A Prodrug of a GluR5 Kainate Receptor Antagonist Active in Two Animal Models of Acute Migraine

Determination of olanzapine in human breast milk by high-performance liquid chromatography with electrochemical detection

Two prodrugs of potent and selective GluR5 kainate receptor antagonists actives in three animal models of pain : 2005 American Chemical Society Award for Computers in Chemical and Pharmaceutical Research

Ethyl (3S, 4aR, 6S, 8aR)-6-(4-ethoxycarbonylimidazol-1-ylmethyl)decahydroisoquinoline-3-c arboxylic ester: A prodrug of a GluR5 kainate receptor antagonist active in two animal models of acute migraine

High Resolution Separation of Urinary Organic Acids by High Performance Liquid Chromatography

Disposition and biotransformation of the antipsychotic agent olanzapine in humans

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