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3-Substituted pyrazoles and 4-substituted triazoles as inhibitors of human 15-lipoxygenase-1

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (15), p.3024-3029

2015

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Efficient synthesis of differently protected methyl (ethyl 1-thio- β- d-glucopyranosid)uronates and their evaluation as glucuronic acid donors and acceptors

Carbohydrate research, 1998-04, Vol.308 (3), p.287-296

1998

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Emerging classes of protein–protein interaction inhibitors and new tools for their development

Current opinion in chemical biology, 2004-08, Vol.8 (4), p.442-449

2004

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High content screening for G protein-coupled receptors using cell-based protein translocation assays

Combinatorial chemistry & high throughput screening, 2005-06, Vol.8 (4), p.301

2005

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N-Substituted pyrazole-3-carboxamides as inhibitors of human 15-lipoxygenase

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (15), p.3017-3023

2015

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Nuclear export inhibitors and kinase inhibitors identified using a MAPK-activated protein kinase 2 redistribution screen

Assay and drug development technologies, 2004-02, Vol.2 (1), p.7-20

2004

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Phosphinic Peptide Matrix Metalloproteinase-9 Inhibitors by Solid-Phase Synthesis Using a Building Block Approach

Chemistry : a European journal, 1999-10, Vol.5 (10), p.2877-2884

1999

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Preparation of an unprotected phosphotyrosine building block and its application in solid-phase synthesis of phosphopeptides

Letters in Peptide Science, 1999-07, Vol.6 (4), p.193-197

1999

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Solid Phase Combinatorial Library of Phosphinic Peptides for Discovery of Matrix Metalloproteinase Inhibitors

Journal of combinatorial chemistry, 2000-11, Vol.2 (6), p.624-638

2000

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Solid phase synthesis of two phosphorylated peptides related to casein using allyl phosphate protection, and their CD spectra

Acta chemica Scandinavica (Copenhagen. 1989), 1996-11, Vol.50 (11), p.1009

1996

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Stereospecific Synthesis of β-d-Fructofuranosides Using the Internal Aglycon Delivery Approach

Journal of organic chemistry, 1996-07, Vol.61 (14), p.4512-4513

1996

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Stereospecific Synthesis of β-d-Fructofuranosides Using Thioglycoside Donors and Internal Aglycon Delivery

Journal of organic chemistry, 1998-03, Vol.63 (6), p.1780-1784

1998

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Syntheses and antiproliferative evaluation of oxyphenisatin derivatives

Bioorganic & medicinal chemistry letters, 2007-05, Vol.17 (10), p.2854-2857

2007

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Synthesis of d-Fructofuranosides Using Thioglycosides as Glycosyl Donors

Journal of organic chemistry, 1996-02, Vol.61 (4), p.1234-1238

1996

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Synthetic strategies to prepare 2-alkyl, 2-aryl and 2-acetylenyl substituted 4,6-diamino-1,3,5-triazines

Tetrahedron letters, 2006-08, Vol.47 (33), p.5973-5975

2006

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3-Substituted pyrazoles and 4-substituted triazoles as inhibitors of human 15-lipoxygenase-1

Efficient synthesis of differently protected methyl (ethyl 1-thio- β- d-glucopyranosid)uronates and their evaluation as glucuronic acid donors and acceptors

Emerging classes of protein–protein interaction inhibitors and new tools for their development

High content screening for G protein-coupled receptors using cell-based protein translocation assays

N-Substituted pyrazole-3-carboxamides as inhibitors of human 15-lipoxygenase

Nuclear export inhibitors and kinase inhibitors identified using a MAPK-activated protein kinase 2 redistribution screen

Phosphinic Peptide Matrix Metalloproteinase-9 Inhibitors by Solid-Phase Synthesis Using a Building Block Approach

Preparation of an unprotected phosphotyrosine building block and its application in solid-phase synthesis of phosphopeptides

Solid Phase Combinatorial Library of Phosphinic Peptides for Discovery of Matrix Metalloproteinase Inhibitors

Solid phase synthesis of two phosphorylated peptides related to casein using allyl phosphate protection, and their CD spectra

Stereospecific Synthesis of β-d-Fructofuranosides Using the Internal Aglycon Delivery Approach

Stereospecific Synthesis of β-d-Fructofuranosides Using Thioglycoside Donors and Internal Aglycon Delivery

Syntheses and antiproliferative evaluation of oxyphenisatin derivatives

Synthesis of d-Fructofuranosides Using Thioglycosides as Glycosyl Donors

Synthetic strategies to prepare 2-alkyl, 2-aryl and 2-acetylenyl substituted 4,6-diamino-1,3,5-triazines

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