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1,4-Dihydropyridines (DHPs) - a class of very potent drugs: syntheses of isotopically labeled DHP derivatives during the last four decades

Journal of labelled compounds & radiopharmaceuticals, 2007-08, Vol.50 (9-10), p.818-830

Pleiss, U.

2007

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Labelling of the guanylate cyclase activator cinaciguat (BAY 58-2667) with carbon-14, tritium and stable isotopes

Journal of labelled compounds & radiopharmaceuticals, 2010-03, Vol.53 (3), p.130-139

2010

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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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Synthesis of [3H] vardenafil, Levitra®, using a new labeling technique

Journal of labelled compounds & radiopharmaceuticals, 2003-11, Vol.46 (13), p.1241-1247

Pleiss, U.

2003

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Syntheses of [2H3, 15N], [14C]Nexavar™ and its labeled metabolites

Journal of labelled compounds & radiopharmaceuticals, 2006-06, Vol.49 (7), p.603-613

2006

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Syntheses of [14C]BAY 59-7939 and its radiolabeled metabolite M-4

Journal of labelled compounds & radiopharmaceuticals, 2006-10, Vol.49 (11), p.929-934

2006

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NO‐ and haem‐independent activation of soluble guanylyl cyclase: molecular basis and cardiovascular implications of a new pharmacological principle

British journal of pharmacology, 2002-07, Vol.136 (5), p.773-783

2002

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Synthesis of a radiolabeled enniatin cyclodepsipeptide [3H-methyl]JES 1798

Journal of labelled compounds & radiopharmaceuticals, 1996-07, Vol.38 (7), p.651-659

1996

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Synthesis of a radiolabeled cyclodepsipeptide [3H-methyl]PF1022A

Journal of labelled compounds & radiopharmaceuticals, 1996-01, Vol.38 (1), p.61-69

1996

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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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Syntheses of [4-14c] and [6-14c]nisoldipine

Journal of labelled compounds & radiopharmaceuticals, 1988-12, Vol.25 (12), p.1393-1400

1988

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Synthesis of (+)-N-(6-Ethoxy[2,4-3H]phenyl)-N-(1,2,2-trimethylpropyl)-2-nitroethene-1,1-diamine ([3H]BAY x 9228)

Journal of labelled compounds & radiopharmaceuticals, 1993-08, Vol.33 (8), p.681-686

1993

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Partial synthesis of [6α-3H]gibberellin-A3 of high specific activity

Journal of labelled compounds & radiopharmaceuticals, 1983-12, Vol.20 (12), p.1413-1414

1983

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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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Partial synthesis of tritium-labelled gibberellin-A3

Journal of labelled compounds & radiopharmaceuticals, 1982-06, Vol.19 (6), p.725-733

1982

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Preparation of tritium-labelled jasmonic acid, ethyl dihydrojasmonate and itaconic acid

Journal of labelled compounds & radiopharmaceuticals, 1983-02, Vol.20 (2), p.205-211

1983

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Synthesis of (+)-(3R)-3-(4-fluorophenylsulfonamido)-1,2,3,4-tetrahydro-9-[5,6,7,8,12,13-U-14C]carbazolepropanoic acid, [14C]BAY u 3405

Journal of labelled compounds & radiopharmaceuticals, 1994-12, Vol.34 (12), p.1207-1215

1994

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Synthesis of N-[4-[2-(2,4-dimethylphenoxy)phenyl]-2-thiazolyl]-hexahydro-2-pyrimidinimine, [14C]BAY w 6341

Journal of labelled compounds & radiopharmaceuticals, 1995-03, Vol.36 (3), p.275-279

1995

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Tritium labelling of nitroaryldihydropyridines

Journal of labelled compounds & radiopharmaceuticals, 1991-09, Vol.29 (9), p.1091-1094

1991

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Synthesis of [3H]cyfluthrin

Journal of labelled compounds & radiopharmaceuticals, 1993-10, Vol.33 (10), p.949-955

1993

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Synthesis of (3R)-3-(4-fluorophenylsulfonamido)-1, 2, 3, 4-tetrahydro-9-[4-3H]carbazolepropanoic acid

Journal of labelled compounds & radiopharmaceuticals, 1990-09, Vol.28 (9), p.1081-1086

1990

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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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Molecular Mechanism of Enantiorecognition of Tertiary Alcohols by Carboxylesterases

Chembiochem : a European journal of chemical biology, 2003-06, Vol.4 (6), p.485-493

2003

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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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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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1,4-Dihydropyridines (DHPs) - a class of very potent drugs: syntheses of isotopically labeled DHP derivatives during the last four decades

Labelling of the guanylate cyclase activator cinaciguat (BAY 58-2667) with carbon-14, tritium and stable isotopes

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

Synthesis of [3H] vardenafil, Levitra®, using a new labeling technique

Syntheses of [2H3, 15N], [14C]Nexavar™ and its labeled metabolites

Syntheses of [14C]BAY 59-7939 and its radiolabeled metabolite M-4

NO‐ and haem‐independent activation of soluble guanylyl cyclase: molecular basis and cardiovascular implications of a new pharmacological principle

Synthesis of a radiolabeled enniatin cyclodepsipeptide [3H-methyl]JES 1798

Synthesis of a radiolabeled cyclodepsipeptide [3H-methyl]PF1022A

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

Syntheses of [4-14c] and [6-14c]nisoldipine

Synthesis of (+)-N-(6-Ethoxy[2,4-3H]phenyl)-N-(1,2,2-trimethylpropyl)-2-nitroethene-1,1-diamine ([3H]BAY x 9228)

Partial synthesis of [6α-3H]gibberellin-A3 of high specific activity

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

Partial synthesis of tritium-labelled gibberellin-A3

Preparation of tritium-labelled jasmonic acid, ethyl dihydrojasmonate and itaconic acid

Synthesis of (+)-(3R)-3-(4-fluorophenylsulfonamido)-1,2,3,4-tetrahydro-9-[5,6,7,8,12,13-U-14C]carbazolepropanoic acid, [14C]BAY u 3405

Synthesis of N-[4-[2-(2,4-dimethylphenoxy)phenyl]-2-thiazolyl]-hexahydro-2-pyrimidinimine, [14C]BAY w 6341

Tritium labelling of nitroaryldihydropyridines

Synthesis of [3H]cyfluthrin

Synthesis of (3R)-3-(4-fluorophenylsulfonamido)-1, 2, 3, 4-tetrahydro-9-[4-3H]carbazolepropanoic acid

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

Molecular Mechanism of Enantiorecognition of Tertiary Alcohols by Carboxylesterases

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

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

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