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Inhibition of Fructose 1,6-Bisphosphatase Reduces Excessive Endogenous Glucose Production and Attenuates Hyperglycemia in Zucker Diabetic Fatty Rats

Diabetes (New York, N.Y.), 2006-06, Vol.55 (6), p.1747-1754

2006

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Antiviral Efficacy upon Administration of a HepDirect Prodrug of 2′-C-Methylcytidine to Hepatitis C Virus-Infected Chimpanzees

Antimicrobial Agents and Chemotherapy, 2011-08, Vol.55 (8), p.3854-3860

2011

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Reduction of hepatic steatosis in rats and mice after treatment with a liver‐targeted thyroid hormone receptor agonist

Hepatology (Baltimore, Md.), 2009-02, Vol.49 (2), p.407-417

2009

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Preclinical pharmacokinetics of a HepDirect prodrug of a novel phosphonate-containing thyroid hormone receptor agonist

Drug metabolism and disposition, 2008-11, Vol.36 (11), p.2393-2403

2008

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Pradefovir: A Prodrug That Targets Adefovir to the Liver for the Treatment of Hepatitis B

Journal of medicinal chemistry, 2008-02, Vol.51 (3), p.666-676

2008

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Adenosine Kinase Inhibitors. 6. Synthesis, Water Solubility, and Antinociceptive Activity of 5-Phenyl-7-(5-deoxy-β-d-ribofuranosyl)pyrrolo[2,3-d]pyrimidines Substituted at C4 with Glycinamides and Related Compounds

Journal of medicinal chemistry, 2005-12, Vol.48 (24), p.7808-7820

2005

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Synthesis and Characterization of a Novel Liver-Targeted Prodrug of Cytosine-1-β-d-arabinofuranoside Monophosphate for the Treatment of Hepatocellular Carcinoma

Journal of medicinal chemistry, 2006-12, Vol.49 (26), p.7711-7720

2006

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Adenosine Kinase Inhibitors. 1. Synthesis, Enzyme Inhibition, and Antiseizure Activity of 5-Iodotubercidin Analogues

Journal of medicinal chemistry, 2000-07, Vol.43 (15), p.2883-2893

2000

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Delivery of high levels of anti-proliferative nucleoside triphosphates to CYP3A-expressing cells as a potential treatment for hepatocellular carcinoma

Cancer chemotherapy and pharmacology, 2009-10, Vol.64 (5), p.981-991

2009

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Adenosine Kinase Inhibitors. 5. Synthesis, Enzyme Inhibition, and Analgesic Activity of Diaryl-erythro-furanosyltubercidin Analogues

Journal of medicinal chemistry, 2005-10, Vol.48 (20), p.6430-6441

2005

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Pharmacologic Profile of CGS 24128, a Potent, Long-Acting Inhibitor of Neutral Endopeptidase 24.11

Journal of cardiovascular pharmacology, 1994-03, Vol.23 (3), p.358-364

1994

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pH- and time-dependent inhibition of rat kidney neutral endoprotease 24.11 by thiorphan and phosphoramidon

Life sciences (1973), 1989, Vol.45 (22), p.2109-2114

1989

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A radioimmunoassay for measuring α-amidating enzyme activity

Analytical biochemistry, 1990-03, Vol.185 (2), p.213-219

1990

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[177Lu-DOTAOTyr3]octreotate: comparison with [111In-DTPAo]octreotide in patients

European Journal of Nuclear Medicine, 2001-09, Vol.28 (9), p.1319-1325

2001

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Inhibition of Fructose 1,6-Bisphosphatase Reduces Excessive Endogenous Glucose Production and Attenuates Hyperglycemia in Zucker Diabetic Fatty Rats

Antiviral Efficacy upon Administration of a HepDirect Prodrug of 2′-C-Methylcytidine to Hepatitis C Virus-Infected Chimpanzees

Reduction of hepatic steatosis in rats and mice after treatment with a liver‐targeted thyroid hormone receptor agonist

Preclinical pharmacokinetics of a HepDirect prodrug of a novel phosphonate-containing thyroid hormone receptor agonist

Pradefovir: A Prodrug That Targets Adefovir to the Liver for the Treatment of Hepatitis B

Adenosine Kinase Inhibitors. 6. Synthesis, Water Solubility, and Antinociceptive Activity of 5-Phenyl-7-(5-deoxy-β-d-ribofuranosyl)pyrrolo[2,3-d]pyrimidines Substituted at C4 with Glycinamides and Related Compounds

Synthesis and Characterization of a Novel Liver-Targeted Prodrug of Cytosine-1-β-d-arabinofuranoside Monophosphate for the Treatment of Hepatocellular Carcinoma

Adenosine Kinase Inhibitors. 1. Synthesis, Enzyme Inhibition, and Antiseizure Activity of 5-Iodotubercidin Analogues

Delivery of high levels of anti-proliferative nucleoside triphosphates to CYP3A-expressing cells as a potential treatment for hepatocellular carcinoma

Adenosine Kinase Inhibitors. 5. Synthesis, Enzyme Inhibition, and Analgesic Activity of Diaryl-erythro-furanosyltubercidin Analogues

Pharmacologic Profile of CGS 24128, a Potent, Long-Acting Inhibitor of Neutral Endopeptidase 24.11

pH- and time-dependent inhibition of rat kidney neutral endoprotease 24.11 by thiorphan and phosphoramidon

A radioimmunoassay for measuring α-amidating enzyme activity

[177Lu-DOTAOTyr3]octreotate: comparison with [111In-DTPAo]octreotide in patients

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