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Pharmacokinetics of BAY 59-7939 - an oral, direct Factor Xa inhibitor - in rats and dogs

Xenobiotica, 2005-09, Vol.35 (9), p.891-910

2005

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Biokinetic model for the calculation of dose coefficients for oral and intravenous administration of 14 C labeled drugs

Kerntechnik (1987), 2022-03, Vol.68 (5-6), p.205-213

2022

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Ribosomal RNA is the target for oxazolidinones, a novel class of translational inhibitors

RNA (Cambridge), 1999-07, Vol.5 (7), p.939-946, Article S1355838299990210

1999

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Inhibition of Hepatitis B Virus Replication by Drug-Induced Depletion of Nucleocapsids

Science (American Association for the Advancement of Science), 2003-02, Vol.299 (5608), p.893-896

2003

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NO-independent regulatory site on soluble guanylate cyclase

Nature (London), 2001-03, Vol.410 (6825), p.212-215

2001

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High Affinity Binding of a Potassium Channel Agonist to Intact Rat Insulinoma Cells

Biochemical and biophysical research communications, 1993-01, Vol.190 (2), p.551-558

1993

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Mode of action of the leukotriene synthesis (FLAP) inhibitor BAY X 1005: implications for biological regulation of 5-lipoxygenase

Agents and Actions, 1994-11, Vol.43 (1-2), p.64-68

1994

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NO-independent regulatory site of direct sGC stimulators like YC-1 and BAY 41-2272

BMC pharmacology, 2001-12, Vol.1 (1), p.13-13, Article 13

2001

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Mode of action of the leukotriene synthesis (FLAP) inhibitor BAY X1005. Implications for biological regulation of 5-lipoxygenase

Advances in prostaglandin, thromboxane, and leukotriene research, 1994, Vol.22, p.23

1994

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Tritium labeling of gonadotropin releasing hormone in its proline and histidine residues

Peptides (New York, N.Y. : 1980), 1981-01, Vol.2 (4), p.445-452

1981

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ChemInform Abstract: THE SYNTHESIS OF 4,4′‐BIS(PHENYLAZO)‐N,N′‐DIPHENYL‐SULFURDIIMIDE

Chemischer Informationsdienst, 1974-11, Vol.5 (47)

1974

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Direct tritium-labelling into histidine of luteinizing hormone-releasing hormone agonists and use of the tracers in studies on proteolytic breakdown

Biochimica et biophysica acta, 1983-12, Vol.761 (2), p.183-190

1983

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Autoradiographic localizatio of [125I]-C-ANP compared to [125I]-ANP in rat tissue

Histochemistry, 1991-08, Vol.96 (4), p.317-321

1991

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Autoradiographic localization of [125I]-C-ANP compared to [125I]-ANP in rat tissue

Histochemistry (Berlin), 1991, Vol.96 (4), p.317-321

1991

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Potent mechanism-based inhibition of human CYP2B6 by clopidogrel and ticlopidine

The Journal of pharmacology and experimental therapeutics, 2004-01, Vol.308 (1), p.189-197

2004

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Peptide–zinc oxide interaction: Finite element simulation using cohesive zone models based on molecular dynamics simulation

Computational materials science, 2014-12, Vol.95, p.320-327

2014

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Preparation and Optimization of a Series of 3-Carboxamido-5-phenacylaminopyrazole Bradykinin B1 Receptor Antagonists

Journal of medicinal chemistry, 2007-10, Vol.50 (21), p.5161-5167

2007

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Improving the permeability of the hydroxyethylamine BACE-1 inhibitors: Structure–activity relationship of P2′ substituents

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (16), p.4789-4794

2010

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Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: Structure–activity relationship of the aryl region

Bioorganic & medicinal chemistry letters, 2010-10, Vol.20 (20), p.6034-6039

2010

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Substrate specificity of lipase B from Candida antarctica in the synthesis of arylaliphatic glycolipids

Journal of molecular catalysis. B, Enzymatic, 2000-02, Vol.8 (4), p.201-211

2000

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Enzymes in lipid modification

Bornscheuer, U. T. (Uwe Theo)

1, 2000

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Multiscale Materials Modeling: Approaches to Full Multiscaling

1, 2016

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Synthesis, characterization and evaluation of pro-drugs of VLA-4 antagonists

Bioorganic & medicinal chemistry letters, 2004-04, Vol.14 (7), p.1651-1654

2004

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Rational evolution of a medium chain-specific cytochrome P-450 BM-3 variant

Biochimica et biophysica acta, 2001-02, Vol.1545 (1-2), p.114-121

2001

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Lipase-catalyzed esterification of unusual substrates : Synthesis of glucuronic acid and ascorbic acid (vitamin C) esters

Biotechnology letters, 1998, Vol.20 (11), p.1091-1094

1998

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Pharmacokinetics of BAY 59-7939 - an oral, direct Factor Xa inhibitor - in rats and dogs

Biokinetic model for the calculation of dose coefficients for oral and intravenous administration of 14 C labeled drugs

Ribosomal RNA is the target for oxazolidinones, a novel class of translational inhibitors

Inhibition of Hepatitis B Virus Replication by Drug-Induced Depletion of Nucleocapsids

NO-independent regulatory site on soluble guanylate cyclase

High Affinity Binding of a Potassium Channel Agonist to Intact Rat Insulinoma Cells

Mode of action of the leukotriene synthesis (FLAP) inhibitor BAY X 1005: implications for biological regulation of 5-lipoxygenase

NO-independent regulatory site of direct sGC stimulators like YC-1 and BAY 41-2272

Mode of action of the leukotriene synthesis (FLAP) inhibitor BAY X1005. Implications for biological regulation of 5-lipoxygenase

Tritium labeling of gonadotropin releasing hormone in its proline and histidine residues

ChemInform Abstract: THE SYNTHESIS OF 4,4′‐BIS(PHENYLAZO)‐N,N′‐DIPHENYL‐SULFURDIIMIDE

Direct tritium-labelling into histidine of luteinizing hormone-releasing hormone agonists and use of the tracers in studies on proteolytic breakdown

Autoradiographic localizatio of [125I]-C-ANP compared to [125I]-ANP in rat tissue

Autoradiographic localization of [125I]-C-ANP compared to [125I]-ANP in rat tissue

Potent mechanism-based inhibition of human CYP2B6 by clopidogrel and ticlopidine

Peptide–zinc oxide interaction: Finite element simulation using cohesive zone models based on molecular dynamics simulation

Preparation and Optimization of a Series of 3-Carboxamido-5-phenacylaminopyrazole Bradykinin B1 Receptor Antagonists

Improving the permeability of the hydroxyethylamine BACE-1 inhibitors: Structure–activity relationship of P2′ substituents

Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: Structure–activity relationship of the aryl region

Substrate specificity of lipase B from Candida antarctica in the synthesis of arylaliphatic glycolipids

Enzymes in lipid modification

Multiscale Materials Modeling: Approaches to Full Multiscaling

Synthesis, characterization and evaluation of pro-drugs of VLA-4 antagonists

Rational evolution of a medium chain-specific cytochrome P-450 BM-3 variant

Lipase-catalyzed esterification of unusual substrates : Synthesis of glucuronic acid and ascorbic acid (vitamin C) esters

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