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SCH 503034, a Mechanism-Based Inhibitor of Hepatitis C Virus NS3 Protease, Suppresses Polyprotein Maturation and Enhances the Antiviral Activity of Alpha Interferon in Replicon Cells

Antimicrobial Agents and Chemotherapy, 2006-03, Vol.50 (3), p.1013-1020

2006

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Synthesis of 3 H, 13 C 2 , 2 H 4 14 C-SCH 430765 and 35 S-SCH 500946, potent and selective inhibitors of the NPY 5 receptor

Journal of labelled compounds & radiopharmaceuticals, 2018-06, Vol.61 (7), p.533-539

2018

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Synthesis of 3H, 13C2, 2H4 14C‐SCH 430765 and 35S‐SCH 500946, potent and selective inhibitors of the NPY5 receptor

Journal of labelled compounds & radiopharmaceuticals, 2018-06, Vol.61 (7), p.533-539

2018

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Synthesis of 3H, 2H4, and 14C‐MK 3814 (preladenant)

Journal of labelled compounds & radiopharmaceuticals, 2017-04, Vol.60 (4), p.194-199

2017

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Synthesis of 3 H, 2 H 4 , and 14 C-MK 3814 (preladenant)

Journal of labelled compounds & radiopharmaceuticals, 2017-04, Vol.60 (4), p.194-199

2017

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Synthesis of (3) H, (2) H4 and (14) C-SCH 417690 (Vicriviroc)

Journal of labelled compounds & radiopharmaceuticals, 2016-05, Vol.59 (5), p.190-196

2016

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Synthesis of 3H, 13C,2H3,15N and 14C-labelled SCH 466036, a histamine 3 receptor antagonist

Journal of labelled compounds & radiopharmaceuticals, 2015-02, Vol.58 (2), p.36-41

2015

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Synthesis of 3H, 2H4 and 14C-SCH 417690 (Vicriviroc)

Journal of labelled compounds & radiopharmaceuticals, 2016-05, Vol.59 (5), p.190-196

2016

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Synthesis of isotopically labelled compounds at Schering-Plough, an historical perspective

Journal of labelled compounds & radiopharmaceuticals, 2007-08, Vol.50 (9-10), p.875-887

2007

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Synthesis of 3H-, 13C3-, and 14C-labeled Sch 727965

Journal of labelled compounds & radiopharmaceuticals, 2011-04, Vol.54 (4), p.196-201

2011

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Deuteration of acetanilides and other substituted aromatics using [Ir(COD)(Cy3P)(Py)]PF6 as catalyst

Journal of labelled compounds & radiopharmaceuticals, 1995-05, Vol.36 (5), p.497-502

1995

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Tritium labelling of pharmaceuticals by metal-catalysed exchange methods

Journal of labelled compounds & radiopharmaceuticals, 2010-09, Vol.53 (11-12), p.722-730

2010

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A simple and efficient synthesis of [3α-3H]5α-androst-16-en-3β-ol

Journal of labelled compounds & radiopharmaceuticals, 2006-10, Vol.49 (11), p.959-963

2006

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Rhodium- and ruthenium-catalysed hydrogen isotope exchange

Journal of labelled compounds & radiopharmaceuticals, 2010-09, Vol.53 (11-12), p.704-715

2010

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Synthesis of [3H], [13C215N] and [14C]Sch 66336 (Sarasar™)

Journal of labelled compounds & radiopharmaceuticals, 2005-01, Vol.48 (1), p.11-23

2005

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Synthesis of 3 H, 13 C2 , 2 H414 C-SCH 430765 and 35 S-SCH 500946, potent and selective inhibitors of the NPY5 receptor

Journal of labelled compounds & radiopharmaceuticals, 2018-06, Vol.61 (7), p.533-539

2018

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Synthesis of 3H, 14C and 2H4 labelled SCH 211803

Journal of labelled compounds & radiopharmaceuticals, 2007-02, Vol.50 (2), p.131-137

2007

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Synthesis of 3 H, 2 H 4 and 14 C-SCH 417690 (Vicriviroc): 3 H, 2 H 4 and 14 C-SCH 417690

Journal of labelled compounds & radiopharmaceuticals, 2016-05, Vol.59 (5), p.190-196

2016

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Synthesis of 3 H, 13 C, 2 H 3 , 15 N and 14 C-labelled SCH 466036, a histamine 3 receptor antagonist: Synthesis of 3H, 13C,2H3,15N and 14C-labelled SCH 466036

Journal of labelled compounds & radiopharmaceuticals, 2015-02, Vol.58 (2), p.36-41

2015

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Biochemical characterization of desloratadine, a potent antagonist of the human histamine H 1 receptor

European journal of pharmacology, 2002-08, Vol.449 (3), p.229-237

2002

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Synthesis of 3 H, 2 H4 , and 14 C-MK 3814 (preladenant)

Journal of labelled compounds & radiopharmaceuticals, 2017-04, Vol.60 (4), p.194-199

2017

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Rhodium- and ruthenium-catalysed hydrogen isotope exchange: Metal-catalysed Hydrogen Isotope Exchange

Journal of labelled compounds & radiopharmaceuticals, 2010, Vol.53 (11-12), p.704-715

2010

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Tritium labelling of pharmaceuticals by metal-catalysed exchange methods: Metal-catalysed Hydrogen Isotope Exchange

Journal of labelled compounds & radiopharmaceuticals, 2010, Vol.53 (11-12), p.722-730

2010

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A rapid method for isolating glandular trichomes

Plant physiology (Bethesda), 1992-05, Vol.99 (1), p.1-7

1992

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Synthesis of 3 H‐, 13 C 3 ‐, and 14 C‐labeled Sch 727965

Journal of labelled compounds & radiopharmaceuticals, 2011-04, Vol.54 (4), p.196-201

2011

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SCH 503034, a Mechanism-Based Inhibitor of Hepatitis C Virus NS3 Protease, Suppresses Polyprotein Maturation and Enhances the Antiviral Activity of Alpha Interferon in Replicon Cells

Synthesis of 3 H, 13 C 2 , 2 H 4 14 C-SCH 430765 and 35 S-SCH 500946, potent and selective inhibitors of the NPY 5 receptor

Synthesis of 3H, 13C2, 2H4 14C‐SCH 430765 and 35S‐SCH 500946, potent and selective inhibitors of the NPY5 receptor

Synthesis of 3H, 2H4, and 14C‐MK 3814 (preladenant)

Synthesis of 3 H, 2 H 4 , and 14 C-MK 3814 (preladenant)

Synthesis of (3) H, (2) H4 and (14) C-SCH 417690 (Vicriviroc)

Synthesis of 3H, 13C,2H3,15N and 14C-labelled SCH 466036, a histamine 3 receptor antagonist

Synthesis of 3H, 2H4 and 14C-SCH 417690 (Vicriviroc)

Synthesis of isotopically labelled compounds at Schering-Plough, an historical perspective

Synthesis of 3H-, 13C3-, and 14C-labeled Sch 727965

Deuteration of acetanilides and other substituted aromatics using [Ir(COD)(Cy3P)(Py)]PF6 as catalyst

Tritium labelling of pharmaceuticals by metal-catalysed exchange methods

A simple and efficient synthesis of [3α-3H]5α-androst-16-en-3β-ol

Rhodium- and ruthenium-catalysed hydrogen isotope exchange

Synthesis of [3H], [13C215N] and [14C]Sch 66336 (Sarasar™)

Synthesis of 3 H, 13 C2 , 2 H414 C-SCH 430765 and 35 S-SCH 500946, potent and selective inhibitors of the NPY5 receptor

Synthesis of 3H, 14C and 2H4 labelled SCH 211803

Synthesis of 3 H, 2 H 4 and 14 C-SCH 417690 (Vicriviroc): 3 H, 2 H 4 and 14 C-SCH 417690

Synthesis of 3 H, 13 C, 2 H 3 , 15 N and 14 C-labelled SCH 466036, a histamine 3 receptor antagonist: Synthesis of 3H, 13C,2H3,15N and 14C-labelled SCH 466036

Biochemical characterization of desloratadine, a potent antagonist of the human histamine H 1 receptor

Synthesis of 3 H, 2 H4 , and 14 C-MK 3814 (preladenant)

Rhodium- and ruthenium-catalysed hydrogen isotope exchange: Metal-catalysed Hydrogen Isotope Exchange

Tritium labelling of pharmaceuticals by metal-catalysed exchange methods: Metal-catalysed Hydrogen Isotope Exchange

A rapid method for isolating glandular trichomes

Synthesis of 3 H‐, 13 C 3 ‐, and 14 C‐labeled Sch 727965

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