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Systemic and intestinal pharmacokinetics of methotrexate in patients with inflammatory bowel disease

Clinical pharmacology and therapeutics, 1999-01, Vol.65 (1), p.29-39

1999

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Synthesis of 1D-3-deoxy-, 1D-2,3-dideoxy-, and 1D-2,3,6-trideoxy-myo-inositol 1,4,5-trisphosphate from quebrachitol, their binding affinities, and calcium release activity

Journal of the American Chemical Society, 1993-06, Vol.115 (11), p.4429-4434

1993

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Inhibition of Recombinant Human Mitochondrial Aldehyde Dehydrogenase by Two Intermediate Metabolites of Disulfiram

Biochemical pharmacology, 1998-04, Vol.55 (7), p.1099-1103

1998

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S-Methyl-N,N-Diethylthiocarbamate Sulfoxide and S-Methyl-N,N-Diethylthiocarbamate Sulfone, Two Candidates for the Active Metabolite of Disulfiram

Alcoholism, clinical and experimental research, 1996-05, Vol.20 (3), p.595-600

1996

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Notch1 augments NF-κB activity by facilitating its nuclear retention

The EMBO journal, 2006-01, Vol.25 (1), p.129-138

2006

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Cellular pharmacology of D-3-azido-3-deoxy-myo-inositol, an inhibitor of phosphatidylinositol signaling having antiproliferative activity

Cancer chemotherapy and pharmacology, 1994-01, Vol.35 (1), p.71-79

1994

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Inhibitors of gamma-secretase block in vivo and in vitro T helper type 1 polarization by preventing Notch upregulation of Tbx21

Nature immunology, 2005-07, Vol.6 (7), p.680-688

2005

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S-Methyl N, N-diethylthiocarbamate sulfone, a potential metabolite of disulfiram and potent inhibitor of low Km mitochondrial aldehyde dehydrogenase

Biochemical pharmacology, 1995-03, Vol.49 (5), p.693-700

1995

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Cloning of a cDNA for Short/Branched Chain Acyl-Coenzyme A Dehydrogenase from Rat and Characterization of Its Tissue Expression and Substrate Specificity

Archives of biochemistry and biophysics, 1996-07, Vol.331 (1), p.127-133

1996

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Adapting a PET Imaging Agent for Correlative Microscopy of Meningiomas and Other Intracranial Tumors

Microscopy and microanalysis, 2012-07, Vol.18 (S2), p.178-179

2012

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D-3-deoxy-3-substituted myo-inositol analogues as inhibitors of cell growth

Cancer chemotherapy and pharmacology, 1991, Vol.29 (2), p.95-104

1991

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Synthesis of Acid-Cleavable Light Isotope-Coded Affinity Tags (ICAT-L) for Potential Use in Proteomic Expression Profiling Analysis

Bioconjugate chemistry, 2006-01, Vol.17 (1), p.248-254

2006

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Design and Chemical Synthesis of a Magnetic Resonance Contrast Agent with Enhanced in Vitro Binding, High Blood−Brain Barrier Permeability, and in Vivo Targeting to Alzheimer's Disease Amyloid Plaques

Biochemistry (Easton), 2004-05, Vol.43 (20), p.6064-6075

2004

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Synthesis and Biological Activity of the D-3-Deoxy-3-fluoro and D-3-Chloro-3-deoxy Analogs of Phosphatidylinositol

Journal of organic chemistry, 1994-03, Vol.59 (5), p.963-971

1994

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Total synthesis of (+)-desepoxyasperdiol

Journal of the American Chemical Society, 1986-03, Vol.108 (5), p.1035-1039

1986

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Deoxygenated inositol 1,4,5-trisphosphate analogs and their interaction with metabolic enzymes. (1R,2R,4R)-Cyclohexane-1,2,4-tris(methylenesulfonate): a potent selective 5-phosphatase inhibitor

Journal of medicinal chemistry, 1993-10, Vol.36 (20), p.3035-3038

1993

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Probing the topography of kainate recognition sites: Synthesis of a novel oxetane containing kainic acid analogue

Tetrahedron letters, 1990, Vol.31 (21), p.2967-2970

1990

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Copper(I)-catalyzed reactions of .beta.,.gamma.-epoxy alcohols with Grignard reagents

Journal of organic chemistry, 1983-11, Vol.48 (22), p.4131-4132

1983

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Molecular recognition at the myo-inositol 1,4,5-trisphosphate receptor. 3-position substituted myo-inositol 1,4,5-trisphosphate analogues reveal the binding and Ca2+ release requirements for high affinity interaction with the myo-inositol 1,4,5-trisphosphate receptor

The Journal of biological chemistry, 1994-10, Vol.269 (43), p.26815-26821

1994

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Cationic cyclopentaannelation: an efficient methylenomycin synthesis

Journal of the American Chemical Society, 1986-06, Vol.108 (12), p.3438-3442

1986

Volltextzugriff (PDF)

[ 125I]Thienylphencyclidine, a novel ligand for the NMDA receptor

European journal of pharmacology, 1992-05, Vol.226 (1), p.53-58

1992

Volltextzugriff (PDF)

Allene ethers for the cationic cyclopentannelation

Tetrahedron letters, 1989, Vol.30 (8), p.923-924

1989

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A Concise, High Yield Synthesis of the Selective ECE-Inhibitor, CGS 35066

Synthetic communications, 2004-12, Vol.34 (5), p.775-782

2004

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Efficacy of Glycoconjugated Dinitroanilines against Cryptosporidium parvum

The Journal of eukaryotic microbiology, 2003-07, Vol.50 (s1), p.550-552

2003

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Efficacy of Glycoconjugated Dinitroanilines against Cryptosporidium Parvum

The Journal of eukaryotic microbiology, 2003-11, Vol.50 (6), p.550-552

2003

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Systemic and intestinal pharmacokinetics of methotrexate in patients with inflammatory bowel disease

Synthesis of 1D-3-deoxy-, 1D-2,3-dideoxy-, and 1D-2,3,6-trideoxy-myo-inositol 1,4,5-trisphosphate from quebrachitol, their binding affinities, and calcium release activity

Inhibition of Recombinant Human Mitochondrial Aldehyde Dehydrogenase by Two Intermediate Metabolites of Disulfiram

S-Methyl-N,N-Diethylthiocarbamate Sulfoxide and S-Methyl-N,N-Diethylthiocarbamate Sulfone, Two Candidates for the Active Metabolite of Disulfiram

Notch1 augments NF-κB activity by facilitating its nuclear retention

Cellular pharmacology of D-3-azido-3-deoxy-myo-inositol, an inhibitor of phosphatidylinositol signaling having antiproliferative activity

Inhibitors of gamma-secretase block in vivo and in vitro T helper type 1 polarization by preventing Notch upregulation of Tbx21

S-Methyl N, N-diethylthiocarbamate sulfone, a potential metabolite of disulfiram and potent inhibitor of low Km mitochondrial aldehyde dehydrogenase

Cloning of a cDNA for Short/Branched Chain Acyl-Coenzyme A Dehydrogenase from Rat and Characterization of Its Tissue Expression and Substrate Specificity

Adapting a PET Imaging Agent for Correlative Microscopy of Meningiomas and Other Intracranial Tumors

D-3-deoxy-3-substituted myo-inositol analogues as inhibitors of cell growth

Synthesis of Acid-Cleavable Light Isotope-Coded Affinity Tags (ICAT-L) for Potential Use in Proteomic Expression Profiling Analysis

Design and Chemical Synthesis of a Magnetic Resonance Contrast Agent with Enhanced in Vitro Binding, High Blood−Brain Barrier Permeability, and in Vivo Targeting to Alzheimer's Disease Amyloid Plaques

Synthesis and Biological Activity of the D-3-Deoxy-3-fluoro and D-3-Chloro-3-deoxy Analogs of Phosphatidylinositol

Total synthesis of (+)-desepoxyasperdiol

Deoxygenated inositol 1,4,5-trisphosphate analogs and their interaction with metabolic enzymes. (1R,2R,4R)-Cyclohexane-1,2,4-tris(methylenesulfonate): a potent selective 5-phosphatase inhibitor

Probing the topography of kainate recognition sites: Synthesis of a novel oxetane containing kainic acid analogue

Copper(I)-catalyzed reactions of .beta.,.gamma.-epoxy alcohols with Grignard reagents

Molecular recognition at the myo-inositol 1,4,5-trisphosphate receptor. 3-position substituted myo-inositol 1,4,5-trisphosphate analogues reveal the binding and Ca2+ release requirements for high affinity interaction with the myo-inositol 1,4,5-trisphosphate receptor

Cationic cyclopentaannelation: an efficient methylenomycin synthesis

[ 125I]Thienylphencyclidine, a novel ligand for the NMDA receptor

Allene ethers for the cationic cyclopentannelation

A Concise, High Yield Synthesis of the Selective ECE-Inhibitor, CGS 35066

Efficacy of Glycoconjugated Dinitroanilines against Cryptosporidium parvum

Efficacy of Glycoconjugated Dinitroanilines against Cryptosporidium Parvum

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