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Structure-based design of substituted hexafluoroisopropanol-arylsulfonamides as modulators of RORc

Bioorganic & medicinal chemistry letters, 2013-12, Vol.23 (24), p.6604-6609

2013

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Discrimination of float glass by LA-ICP-MS: assessment of exclusion criteria using casework samples

Journal - Canadian Society of Forensic Science, 2015-04, Vol.48 (2), p.85-96

2015

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Unusual Variation of Thickness Within a Pane of Annealed Float Glass

Journal - Canadian Society of Forensic Science, 2013-01, Vol.46 (3), p.166-169

2013

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Discovery of LRRK2 inhibitors by using an ensemble of virtual screening methods

Bioorganic & medicinal chemistry letters, 2017-06, Vol.27 (11), p.2520-2527

2017

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Reduction in lipophilicity improved the solubility, plasma–protein binding, and permeability of tertiary sulfonamide RORc inverse agonists

Bioorganic & medicinal chemistry letters, 2014-08, Vol.24 (16), p.3891-3897

2014

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Minor Structural Change to Tertiary Sulfonamide RORc Ligands Led to Opposite Mechanisms of Action

ACS medicinal chemistry letters, 2015-03, Vol.6 (3), p.276-281

2015

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Identification of tertiary sulfonamides as RORc inverse agonists

Bioorganic & medicinal chemistry letters, 2014-05, Vol.24 (9), p.2182-2187

2014

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Discovery of Novel Allosteric Mitogen-Activated Protein Kinase Kinase (MEK) 1,2 Inhibitors Possessing Bidentate Ser212 Interactions

Journal of medicinal chemistry, 2012-05, Vol.55 (10), p.4594-4604

2012

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Structure based design of novel 6,5 heterobicyclic mitogen-activated protein kinase kinase (MEK) inhibitors leading to the discovery of imidazo[1,5-a] pyrazine G-479

Bioorganic & medicinal chemistry letters, 2014-10, Vol.24 (19), p.4714-4723

2014

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Identification of N-sulfonyl-tetrahydroquinolines as RORc inverse agonists

Bioorganic & medicinal chemistry letters, 2015-10, Vol.25 (19), p.4109-4113

2015

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Mitigation of Acetylcholine Esterase Activity in the 1,7-Diazacarbazole Series of Inhibitors of Checkpoint Kinase 1

Journal of medicinal chemistry, 2015-06, Vol.58 (12), p.5053-5074

2015

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Abstract 5137: Parallel approaches to the discovery of novel BRD4 inhibitors

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.5137-5137

2014

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Syntheses of [ 3 H 2 ]T0901317 and a labeled structural isomer, and characterization of the dispersed labeled compounds via 19 F NMR

Journal of labelled compounds & radiopharmaceuticals, 2014-01, Vol.57 (1), p.57-60

2014

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Syntheses of [3H2]T0901317 and a labeled structural isomer, and characterization of the dispersed labeled compounds via 19F NMR

Journal of labelled compounds & radiopharmaceuticals, 2014-01, Vol.57 (1), p.57-60

2014

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5-Aminopyrimidin-2-ylnitriles as Cathepsin K inhibitors

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (6), p.1658-1661

2009

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The discovery of RPR 200765A, a p38 MAP kinase inhibitor displaying a good oral anti-arthritic efficacy

Bioorganic & medicinal chemistry, 2001-02, Vol.9 (2), p.537-554

2001

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Multidimensional classrooms: Developing a comprehensive research base for holistic education

Grimes, Brenda Burton

2007

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ProQuest

Law Firm Librarianship

Encyclopedia of Library and Information Sciences, 2018, p.2705-2709

4, 2018

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Family members'perception of the quality of nursing home care

International journal of geriatric psychiatry, 1995-09, Vol.10 (9), p.787-796

1995

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Hypolipidaemic properties of a potent and bioavailable alkylsulphinyl-diphenylimidazole ACAT inhibitor (RP 73163) in animals fed diets low in cholesterol

Biochemical pharmacology, 1996-10, Vol.52 (8), p.1177-1186

1996

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Institutional Loyalty and Job Satisfaction among Nurse Aides in Nursing Homes

Journal of aging and health, 1991-02, Vol.3 (1), p.47-65

1991

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RP 64477: A potent inhibitor of acyl-coenzyme A: Cholesterol O-acyltransferase with low systemic bioavailability

Biochemical pharmacology, 1996-02, Vol.51 (4), p.413-421

1996

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RP 64477: A potent inhibitor of acyl-coenzyme A

Biochemical pharmacology, 1996-02, Vol.51 (4), p.413-421

1996

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Virtual Reality for Distraction in Adolescent Lumbar Punctures

Journal of pediatric oncology nursing, 1999-04, Vol.16 (2), p.98-98

1999

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Virtual reality for distraction in adolescent lumbar punctures

Journal of pediatric oncology nursing, 1999-04, Vol.16 (2), p.98-98

1999

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Structure-based design of substituted hexafluoroisopropanol-arylsulfonamides as modulators of RORc

Discrimination of float glass by LA-ICP-MS: assessment of exclusion criteria using casework samples

Unusual Variation of Thickness Within a Pane of Annealed Float Glass

Discovery of LRRK2 inhibitors by using an ensemble of virtual screening methods

Reduction in lipophilicity improved the solubility, plasma–protein binding, and permeability of tertiary sulfonamide RORc inverse agonists

Minor Structural Change to Tertiary Sulfonamide RORc Ligands Led to Opposite Mechanisms of Action

Identification of tertiary sulfonamides as RORc inverse agonists

Discovery of Novel Allosteric Mitogen-Activated Protein Kinase Kinase (MEK) 1,2 Inhibitors Possessing Bidentate Ser212 Interactions

Structure based design of novel 6,5 heterobicyclic mitogen-activated protein kinase kinase (MEK) inhibitors leading to the discovery of imidazo[1,5-a] pyrazine G-479

Identification of N-sulfonyl-tetrahydroquinolines as RORc inverse agonists

Mitigation of Acetylcholine Esterase Activity in the 1,7-Diazacarbazole Series of Inhibitors of Checkpoint Kinase 1

Abstract 5137: Parallel approaches to the discovery of novel BRD4 inhibitors

Syntheses of [ 3 H 2 ]T0901317 and a labeled structural isomer, and characterization of the dispersed labeled compounds via 19 F NMR

Syntheses of [3H2]T0901317 and a labeled structural isomer, and characterization of the dispersed labeled compounds via 19F NMR

5-Aminopyrimidin-2-ylnitriles as Cathepsin K inhibitors

The discovery of RPR 200765A, a p38 MAP kinase inhibitor displaying a good oral anti-arthritic efficacy

Multidimensional classrooms: Developing a comprehensive research base for holistic education

Law Firm Librarianship

Family members'perception of the quality of nursing home care

Hypolipidaemic properties of a potent and bioavailable alkylsulphinyl-diphenylimidazole ACAT inhibitor (RP 73163) in animals fed diets low in cholesterol

Institutional Loyalty and Job Satisfaction among Nurse Aides in Nursing Homes

RP 64477: A potent inhibitor of acyl-coenzyme A: Cholesterol O-acyltransferase with low systemic bioavailability

RP 64477: A potent inhibitor of acyl-coenzyme A

Virtual Reality for Distraction in Adolescent Lumbar Punctures

Virtual reality for distraction in adolescent lumbar punctures

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