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Sequences with Low‐Discrepancy Blue‐Noise 2‐D Projections

Computer graphics forum, 2018-05, Vol.37 (2), p.339-353

2018

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Low-discrepancy blue noise sampling

ACM transactions on graphics, 2016-11, Vol.35 (6), p.1-13

2016

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Blue-noise sampling for human retinal cone spatial distribution modeling

Journal of physics communications, 2020-03, Vol.4 (3), p.35013

2020

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5-lipoxygenase-activating protein is an arachidonate binding protein

FEBS letters, 1993-03, Vol.318 (3), p.277-281

1993

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NMR structural studies of the tight complex between a trifluoromethyl ketone inhibitor and the 85-kDa human phospholipase A2

Biochemistry (Easton), 1993-11, Vol.32 (47), p.12560-12565

1993

Volltextzugriff (PDF)

Substituted 2,2-bisaryl-bicycloheptanes as novel and potent inhibitors of 5-lipoxygenase activating protein

Bioorganic & medicinal chemistry, 2008-03, Vol.18 (6), p.2023-2027

2008

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Slow- and tight-binding inhibitors of the 85-kDa human phospholipase A2

Biochemistry (Easton), 1993-06, Vol.32 (23), p.5935-5940

1993

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Design, synthesis, and biological evaluation of 8-biarylquinolines: A novel class of PDE4 inhibitors

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (4), p.1407-1412

2008

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Interspecies in vitro metabolism of the phosphodiesterase-4 (PDE4) inhibitor L-454,560

Journal of mass spectrometry., 2006-06, Vol.41 (6), p.771-780

2006

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Arachidonyl trifluoromethyl ketone, a potent inhibitor of 85-kDa phospholipase A2, blocks production of arachidonate and 12-hydroxyeicosatetraenoic acid by calcium ionophore-challenged platelets

The Journal of biological chemistry, 1994-06, Vol.269 (22), p.15619-15624

1994

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Liquid-Phase Synthesis with Solid-Phase Workup: Application to Multistep and Combinatorial Syntheses

Journal of organic chemistry, 1999-03, Vol.64 (6), p.2110-2113

1999

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Nitrogen-bridged substituted 8-arylquinolines as potent PDE IV inhibitors

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (10), p.2608-2612

2006

Volltextzugriff (PDF)

Interactive Curvature Tensor Visualization on Digital Surfaces

Discrete Geometry for Computer Imagery, p.282-294

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Synthesis of Rofecoxib, (MK 0966, Vioxx ® 4-(4′-Methylsulfonylphenyl)-3-Phenyl-2(5H)-Furanone), a Selective and Orally Active Inhibitor of Cyclooxygenase-2

Synthesis (Stuttgart), 2001, Vol.2001 (12), p.1778-1779

2001

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Investigation of the in vitro metabolism profile of a phosphodiesterase-IV inhibitor, CDP-840: leading to structural optimization

Drug metabolism and disposition, 2001-03, Vol.29 (3), p.232

2001

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Analyse des non-conformités d’une préparation radiopharmaceutique : le 99MTC-mertiatide

Le pharmacien hospitalier & clinicien, 2017-12, Vol.52 (4), p.397-397

2017

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Hunting the Emesis and Efficacy Targets of PDE4 Inhibitors: Identification of the Photoaffinity Probe 8-(3-Azidophenyl)-6- [(4-iodo-1H-1-imidazolyl)methyl]quinoline (APIIMQ)

Journal of medicinal chemistry, 2000-10, Vol.43 (21), p.3820-3823

2000

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Solid phase parallel synthesis of highly substituted thiophene derivatives and identification of novel phosphodiesterase-4 (PDE-4) inhibitors

Tetrahedron, 1999-09, Vol.55 (39), p.11669-11685

1999

Volltextzugriff (PDF)

[1,3] and [3,3] rearrangements of 3-amino-1,5-hexadienes: Solvent effect on the regioselectivity

Tetrahedron letters, 1999-04, Vol.40 (16), p.3119-3122

1999

Volltextzugriff (PDF)

Synthesis and preparation of an affinity chromatography column for the purification of cytosolic phospholipase A2

Bioorganic & medicinal chemistry letters, 1995-03, Vol.5 (5), p.519-522

1995

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Continuous, Vesicle-Based Fluorimetric Assays of 14- and 85-kDa Phospholipases A2

Analytical biochemistry, 1995-11, Vol.232 (1), p.7-23

1995

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Substituted furans as inhibitors of the PDE4 enzyme

Bioorganic & medicinal chemistry letters, 1999-02, Vol.9 (3), p.323-326

1999

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Synthesis and preparation of an affinity chromatography column for the purification of cytosolic phospholipase A 2

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (5), p.519-522

1995

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Sequences with Low‐Discrepancy Blue‐Noise 2‐D Projections

Low-discrepancy blue noise sampling

Blue-noise sampling for human retinal cone spatial distribution modeling

5-lipoxygenase-activating protein is an arachidonate binding protein

NMR structural studies of the tight complex between a trifluoromethyl ketone inhibitor and the 85-kDa human phospholipase A2

Substituted 2,2-bisaryl-bicycloheptanes as novel and potent inhibitors of 5-lipoxygenase activating protein

Slow- and tight-binding inhibitors of the 85-kDa human phospholipase A2

Design, synthesis, and biological evaluation of 8-biarylquinolines: A novel class of PDE4 inhibitors

Interspecies in vitro metabolism of the phosphodiesterase-4 (PDE4) inhibitor L-454,560

Arachidonyl trifluoromethyl ketone, a potent inhibitor of 85-kDa phospholipase A2, blocks production of arachidonate and 12-hydroxyeicosatetraenoic acid by calcium ionophore-challenged platelets

Liquid-Phase Synthesis with Solid-Phase Workup: Application to Multistep and Combinatorial Syntheses

Nitrogen-bridged substituted 8-arylquinolines as potent PDE IV inhibitors

Discovery of a substituted 8-arylquinoline series of PDE4 inhibitors: Structure–activity relationship, optimization, and identification of a highly potent, well tolerated, PDE4 inhibitor

Interactive Curvature Tensor Visualization on Digital Surfaces

Synthesis of Rofecoxib, (MK 0966, Vioxx ® 4-(4′-Methylsulfonylphenyl)-3-Phenyl-2(5H)-Furanone), a Selective and Orally Active Inhibitor of Cyclooxygenase-2

Investigation of the in vitro metabolism profile of a phosphodiesterase-IV inhibitor, CDP-840: leading to structural optimization

Analyse des non-conformités d’une préparation radiopharmaceutique : le 99MTC-mertiatide

Hunting the Emesis and Efficacy Targets of PDE4 Inhibitors: Identification of the Photoaffinity Probe 8-(3-Azidophenyl)-6- [(4-iodo-1H-1-imidazolyl)methyl]quinoline (APIIMQ)

Solid phase parallel synthesis of highly substituted thiophene derivatives and identification of novel phosphodiesterase-4 (PDE-4) inhibitors

Discovery of a substituted 8-arylquinoline series of PED4 inhibitors : Structure-activity relationship, optimization, and identification of a highly potent, well tolerated, PDE4 inhibitor

[1,3] and [3,3] rearrangements of 3-amino-1,5-hexadienes: Solvent effect on the regioselectivity

Synthesis and preparation of an affinity chromatography column for the purification of cytosolic phospholipase A2

Continuous, Vesicle-Based Fluorimetric Assays of 14- and 85-kDa Phospholipases A2

Substituted furans as inhibitors of the PDE4 enzyme

Synthesis and preparation of an affinity chromatography column for the purification of cytosolic phospholipase A 2

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