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Transport of the dipeptidyl peptidase-4 inhibitor sitagliptin by human organic anion transporter 3, organic anion transporting polypeptide 4C1, and multidrug resistance P-glycoprotein

The Journal of pharmacology and experimental therapeutics, 2007-05, Vol.321 (2), p.673

2007

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Evaluation of ubiquinone concentration and mitochondrial function relative to cerivastatin-induced skeletal myopathy in rats

Toxicology and applied pharmacology, 2004, Vol.194 (1), p.10-23

2004

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In vitro metabolic activation of lumiracoxib in rat and human liver preparations

Drug metabolism and disposition, 2008-02, Vol.36 (2), p.469

2008

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The Target of Ezetimibe Is Niemann-Pick C1-Like 1 (NPC1L1)

Proceedings of the National Academy of Sciences - PNAS, 2005-06, Vol.102 (23), p.8132-8137

2005

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Metabolites of caspofungin acetate, a potent antifungal agent, in human plasma and urine

Drug metabolism and disposition, 2000-11, Vol.28 (11), p.1274

2000

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Structural Requirements for the Activation of the Human Growth Hormone Secretagogue Receptor by Peptide and Nonpeptide Secretagogues

Molecular endocrinology (Baltimore, Md.), 1998-01, Vol.12 (1), p.137-145

1998

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Validation of (-)-N-3-benzyl-phenobarbital as a selective inhibitor of CYP2C19 in human liver microsomes

Drug metabolism and disposition, 2004-06, Vol.32 (6), p.584

2004

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Fluoroolefins as amide bond mimics in dipeptidyl peptidase IV inhibitors

Bioorganic & medicinal chemistry, 2008-04, Vol.18 (7), p.2409-2413

2008

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Comparative Assessment of the Ligand and Metal Ion Binding Properties of Integrins α9β1 and α4β1

Biochemistry (Easton), 2002-06, Vol.41 (22), p.7125-7141

2002

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Pharmacokinetics, metabolism, and excretion of anacetrapib, a novel inhibitor of the cholesteryl ester transfer protein, in rats and rhesus monkeys

Drug metabolism and disposition, 2010-03, Vol.38 (3), p.459

2010

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Metabolism and excretion of anacetrapib, a novel inhibitor of the cholesteryl ester transfer protein, in humans

Drug metabolism and disposition, 2010-03, Vol.38 (3), p.474

2010

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The changing environment of graduate and postdoctoral training in drug metabolism: viewpoints from academia, industry, and government

Drug metabolism and disposition, 2003-04, Vol.31 (4), p.360

2003

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Ivermectin and Nodulisporic Acid Receptors in Drosophila melanogaster Contain Both γ-Aminobutyric Acid-Gated Rdl and Glutamate-Gated GluClα Chloride Channel Subunits

Biochemistry (Easton), 2002-05, Vol.41 (20), p.6548-6560

2002

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Identification of metabolites of a substance P (neurokinin 1 receptor) antagonist in rat hepatocytes and rat plasma

Drug metabolism and disposition, 2002-08, Vol.30 (8), p.937

2002

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Studies on cytochrome P-450-mediated bioactivation of diclofenac in rats and in human hepatocytes: identification of glutathione conjugated metabolites

Drug metabolism and disposition, 1999-03, Vol.27 (3), p.365

1999

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Synthesis of Functionalized Azomethine Ylides via the Rh(II)-Catalyzed Cyclization of .alpha.-Diazo Carbonyls onto Imino .pi.-Bonds

Journal of organic chemistry, 1994-09, Vol.59 (18), p.5347-5357

1994

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Identification of potent agonists of photoreceptor-specific nuclear receptor (NR2E3) and preparation of a radioligand

Bioorganic & medicinal chemistry letters, 2006-10, Vol.16 (19), p.5001-5004

2006

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Multiple strategies for the preparation of a sulfur-35 labeled NPC1L1 radioligand

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (17), p.5033-5036

2009

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Synthesis of the first sulfur-35-labeled hERG radioligand

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (6), p.1692-1695

2006

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The absorption, distribution, metabolism and excretion of rofecoxib, a potent and selective cyclooxygenase-2 inhibitor, in rats and dogs

Drug metabolism and disposition, 2000-10, Vol.28 (10), p.1244

2000

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Interaction of diclofenac and quinidine in monkeys: stimulation of diclofenac metabolism

The Journal of pharmacology and experimental therapeutics, 1999-12, Vol.291 (3), p.1068

1999

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Vinylogous carbinolamine tumor inhibitors. 24. Synthesis, chemistry, and antineoplastic activity of .alpha.-halopyridinium salts: potential pyridone prodrugs of acylated vinylogous carbinolamine tumor inhibitors

Journal of medicinal chemistry, 1990-06, Vol.33 (6), p.1667-1675

1990

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Azomethine ylide generation via the rhodium(II)-induced cyclization reaction of oximino .alpha.-diazo ketones

Journal of organic chemistry, 1990-01, Vol.55 (2), p.405-406

1990

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A Photoactivatable Prenylated Cysteine Designed to Study Isoprenoid Recognition

Journal of the American Chemical Society, 2001-05, Vol.123 (19), p.4373-4381

2001

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A nonpeptide oxytocin receptor antagonist radioligand highly selective for human receptors

European journal of pharmacology, 2002-08, Vol.450 (1), p.19-28

2002

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Transport of the dipeptidyl peptidase-4 inhibitor sitagliptin by human organic anion transporter 3, organic anion transporting polypeptide 4C1, and multidrug resistance P-glycoprotein

Evaluation of ubiquinone concentration and mitochondrial function relative to cerivastatin-induced skeletal myopathy in rats

In vitro metabolic activation of lumiracoxib in rat and human liver preparations

The Target of Ezetimibe Is Niemann-Pick C1-Like 1 (NPC1L1)

Metabolites of caspofungin acetate, a potent antifungal agent, in human plasma and urine

Structural Requirements for the Activation of the Human Growth Hormone Secretagogue Receptor by Peptide and Nonpeptide Secretagogues

Validation of (-)-N-3-benzyl-phenobarbital as a selective inhibitor of CYP2C19 in human liver microsomes

Fluoroolefins as amide bond mimics in dipeptidyl peptidase IV inhibitors

Comparative Assessment of the Ligand and Metal Ion Binding Properties of Integrins α9β1 and α4β1

Pharmacokinetics, metabolism, and excretion of anacetrapib, a novel inhibitor of the cholesteryl ester transfer protein, in rats and rhesus monkeys

Metabolism and excretion of anacetrapib, a novel inhibitor of the cholesteryl ester transfer protein, in humans

The changing environment of graduate and postdoctoral training in drug metabolism: viewpoints from academia, industry, and government

Ivermectin and Nodulisporic Acid Receptors in Drosophila melanogaster Contain Both γ-Aminobutyric Acid-Gated Rdl and Glutamate-Gated GluClα Chloride Channel Subunits

Identification of metabolites of a substance P (neurokinin 1 receptor) antagonist in rat hepatocytes and rat plasma

Studies on cytochrome P-450-mediated bioactivation of diclofenac in rats and in human hepatocytes: identification of glutathione conjugated metabolites

Synthesis of Functionalized Azomethine Ylides via the Rh(II)-Catalyzed Cyclization of .alpha.-Diazo Carbonyls onto Imino .pi.-Bonds

Identification of potent agonists of photoreceptor-specific nuclear receptor (NR2E3) and preparation of a radioligand

Multiple strategies for the preparation of a sulfur-35 labeled NPC1L1 radioligand

Synthesis of the first sulfur-35-labeled hERG radioligand

The absorption, distribution, metabolism and excretion of rofecoxib, a potent and selective cyclooxygenase-2 inhibitor, in rats and dogs

Interaction of diclofenac and quinidine in monkeys: stimulation of diclofenac metabolism

Vinylogous carbinolamine tumor inhibitors. 24. Synthesis, chemistry, and antineoplastic activity of .alpha.-halopyridinium salts: potential pyridone prodrugs of acylated vinylogous carbinolamine tumor inhibitors

Azomethine ylide generation via the rhodium(II)-induced cyclization reaction of oximino .alpha.-diazo ketones

A Photoactivatable Prenylated Cysteine Designed to Study Isoprenoid Recognition

A nonpeptide oxytocin receptor antagonist radioligand highly selective for human receptors

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