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The specificity of JAK3 kinase inhibitors

Blood, 2008-02, Vol.111 (4), p.2155-2157

2008

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Structure of the Catalytic Domain of Human Polo-like Kinase 1

Biochemistry (Easton), 2007-05, Vol.46 (20), p.5960-5971

2007

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Investigation of the binding pocket of human hematopoietic prostaglandin (PG) D2 synthase (hH-PGDS): A tale of two waters

Bioorganic & medicinal chemistry letters, 2012-06, Vol.22 (11), p.3795-3799

2012

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Bipiperidinyl Carboxylic Acid Amides as Potent, Selective, and Functionally Active CCR4 Antagonists

Chemical biology & drug design, 2007-09, Vol.70 (3), p.268-272

2007

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Research Article: Selectivity-determining Residues in Plk1

Chemical biology & drug design, 2007-12, Vol.70 (6), p.540-546

2007

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Selectivity-determining Residues in Plk1

Chemical biology & drug design, 2007-12, Vol.70 (6), p.540-546

2007

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Design, synthesis and biological evaluation of novel aminothiazoles as antiviral compounds acting against human rhinovirus

Bioorganic & medicinal chemistry letters, 2013-07, Vol.23 (13), p.3841-3847

2013

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Potent and selective thiophene urea-templated inhibitors of S6K

Bioorganic & medicinal chemistry letters, 2011-01, Vol.21 (2), p.849-852

2011

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Identification of benzofurano[3,2-d]pyrimidin-2-ones, a new series of HIV-1 nucleotide-competing reverse transcriptase inhibitors

Bioorganic & medicinal chemistry letters, 2013-05, Vol.23 (9), p.2775-2780

2013

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Discovery of Potent, Orally Bioavailable Inhibitors of Human Cytomegalovirus

ACS medicinal chemistry letters, 2016-05, Vol.7 (5), p.525-530

2016

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Selective cell adhesion inhibitors: Barbituric acid based α4β7—MAdCAM inhibitors

Bioorganic & medicinal chemistry letters, 2008-04, Vol.18 (7), p.2509-2512

2008

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Selective cell adhesion inhibitors: Barbituric acid based alpha 4 beta 7 - MAdCAM inhibitors

Bioorganic & medicinal chemistry, 2008-04, Vol.18 (7), p.2509-2512

2008

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Enhanced selectivity profile of pyrazole-urea based DFG-out p38α inhibitors

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (16), p.4885-4891

2010

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Enhanced selectivity profile of pyrazole-urea based DFG-out p38a inhibitors

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (16), p.4885-4891

2010

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Design, Synthesis and Potential Utility of Fluorescence Probes that Target DFG-out Conformation of p38α for High Throughput Screening Binding Assay

Chemical biology & drug design, 2009-12, Vol.74 (6), p.547-559

2009

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Domino Aza-Claisen/Mannich Cyclization Reaction from a Chiral α-Alkoxy Enamine or Sequential Alkylation of an α-Alkoxy Ester Enolate or Nitrile Anion, Followed by an Intramolecular Wittig Reaction: Two (3+2) Annulation Routes to Homochiral 4-Alkyl-4-hydroxy-2-cyclopentenone Synthesis

European journal of organic chemistry, 2003-07, Vol.2003 (14), p.2585-2595

2003

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Synthesis and biological evaluation of new cross-conjugated dienone marine prostanoid analogues

Organic & biomolecular chemistry, 2004-07, Vol.2 (14), p.2028-2039

2004

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Solid-Phase Enolate Chemistry Investigated Using HR-MAS NMR Spectroscopy

Journal of organic chemistry, 2002-01, Vol.67 (2), p.526-532

2002

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Efficient Use of the Iron Ortho-Nitrophenylporphyrin Chloride to Mimic Biological Oxidations of Dimethylaminoantipyrine

Chemical biology & drug design, 2007-10, Vol.70 (4), p.354-359

2007

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Synthesis and biological evaluation of new cross-conjugated dienone marine prostanoid analoguesElectronic supplementary information (ESI) available: 1H NMR, COSY and NOESY spectra. See http://www.rsc.org/suppdata/ob/b4/b404016c

Organic & biomolecular chemistry, 2004, Vol.2 (14), p.2028

2004

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Enhanced selectivity profile of pyrazole-urea based DFG-out p38alpha inhibitors

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (16), p.4885-4891

2010

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A carbohydrate approach to 4-hydroxy-2-cyclopentenone moiety of antitumor prostanoid Punaglandin IV via alkylation of ester uronate

Tetrahedron letters, 1998-06, Vol.39 (24), p.4247-4250

1998

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Chameleon catches in combinatorial chemistry: Tebbe olefination of polymer supported esters and the synthesis of amines, cyclohexanones, enones, methyl ketones and thiazoles

Chemical communications (Cambridge, England), 1998-09 (18), p.2019-2020

1998

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The design, synthesis and potential utility of fluorescence probes that target DFG-out conformation of p38alpha for high throughput screening binding assay

Chemical biology & drug design, 2009-12, Vol.74 (6), p.547-559

2009

Volltextzugriff (PDF)

Selective cell adhesion inhibitors: Barbituric acid based alpha4beta7--MAdCAM inhibitors

Bioorganic & medicinal chemistry letters, 2008-04, Vol.18 (7), p.2509-2512

2008

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The specificity of JAK3 kinase inhibitors

Structure of the Catalytic Domain of Human Polo-like Kinase 1

Investigation of the binding pocket of human hematopoietic prostaglandin (PG) D2 synthase (hH-PGDS): A tale of two waters

Bipiperidinyl Carboxylic Acid Amides as Potent, Selective, and Functionally Active CCR4 Antagonists

Research Article: Selectivity-determining Residues in Plk1

Selectivity-determining Residues in Plk1

Design, synthesis and biological evaluation of novel aminothiazoles as antiviral compounds acting against human rhinovirus

Potent and selective thiophene urea-templated inhibitors of S6K

Identification of benzofurano[3,2-d]pyrimidin-2-ones, a new series of HIV-1 nucleotide-competing reverse transcriptase inhibitors

Discovery of Potent, Orally Bioavailable Inhibitors of Human Cytomegalovirus

Selective cell adhesion inhibitors: Barbituric acid based α4β7—MAdCAM inhibitors

Selective cell adhesion inhibitors: Barbituric acid based alpha 4 beta 7 - MAdCAM inhibitors

Enhanced selectivity profile of pyrazole-urea based DFG-out p38α inhibitors

Enhanced selectivity profile of pyrazole-urea based DFG-out p38a inhibitors

Design, Synthesis and Potential Utility of Fluorescence Probes that Target DFG-out Conformation of p38α for High Throughput Screening Binding Assay

Domino Aza-Claisen/Mannich Cyclization Reaction from a Chiral α-Alkoxy Enamine or Sequential Alkylation of an α-Alkoxy Ester Enolate or Nitrile Anion, Followed by an Intramolecular Wittig Reaction: Two (3+2) Annulation Routes to Homochiral 4-Alkyl-4-hydroxy-2-cyclopentenone Synthesis

Synthesis and biological evaluation of new cross-conjugated dienone marine prostanoid analogues

Solid-Phase Enolate Chemistry Investigated Using HR-MAS NMR Spectroscopy

Efficient Use of the Iron Ortho-Nitrophenylporphyrin Chloride to Mimic Biological Oxidations of Dimethylaminoantipyrine

Synthesis and biological evaluation of new cross-conjugated dienone marine prostanoid analoguesElectronic supplementary information (ESI) available: 1H NMR, COSY and NOESY spectra. See http://www.rsc.org/suppdata/ob/b4/b404016c

Enhanced selectivity profile of pyrazole-urea based DFG-out p38alpha inhibitors

A carbohydrate approach to 4-hydroxy-2-cyclopentenone moiety of antitumor prostanoid Punaglandin IV via alkylation of ester uronate

Chameleon catches in combinatorial chemistry: Tebbe olefination of polymer supported esters and the synthesis of amines, cyclohexanones, enones, methyl ketones and thiazoles

The design, synthesis and potential utility of fluorescence probes that target DFG-out conformation of p38alpha for high throughput screening binding assay

Selective cell adhesion inhibitors: Barbituric acid based alpha4beta7--MAdCAM inhibitors

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