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Solid-Phase Extraction and Quantitative Measurement of Omega and Omega-1 Metabolites of JWH-018 and JWH-073 in Human Urine

Analytical chemistry (Washington), 2011-08, Vol.83 (16), p.6381-6388

2011

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Akt activation improves oxidative phosphorylation in renal proximal tubular cells following nephrotoxicant injury

American journal of physiology. Renal physiology, 2008-02, Vol.294 (2), p.F423-F432

2008

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Protein kinase B/Akt modulates nephrotoxicant-induced necrosis in renal cells

American journal of physiology. Renal physiology, 2007-01, Vol.292 (1), p.F292-F303

2007

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Acetaminophen-induced hepatotoxicity in mice occurs with inhibition of activity and nitration of mitochondrial manganese superoxide dismutase

The Journal of pharmacology and experimental therapeutics, 2011-04, Vol.337 (1), p.110-118

2011

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Clinically Relevant Herb-Micronutrient Interactions: When Botanicals, Minerals, and Vitamins Collide

Advances in nutrition (Bethesda, Md.), 2018-07, Vol.9 (4), p.524S-532S

2018

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Hydrastine pharmacokinetics and metabolism after a single oral dose of goldenseal (Hydrastis canadensis) to humans

Drug metabolism and disposition, 2015-04, Vol.43 (4), p.534-552

2015

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Drug-Organic Electrolyte Complexes as Controlled Release Systems

Drug development and industrial pharmacy, 2009-01, Vol.35 (1), p.1-11

2009

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Cooperativity in CYP2E1 metabolism of acetaminophen and styrene mixtures

Biochemical pharmacology, 2015-10, Vol.97 (3), p.341-349

2015

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Multiple modes of α7 nAChR noncompetitive antagonism of control agonist-evoked and allosterically enhanced currents

Molecular pharmacology, 2013-09, Vol.84 (3), p.459-475

2013

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Crystal structure of 4,4'-bis-[3-(piperidin-1-yl)prop-1-yn-1-yl]-1,1'-biphen-yl

Acta crystallographica. Section E, Crystallographic communications, 2017-06, Vol.73 (Pt 6), p.864-866

2017

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Crystal structure of 4,4′-bis[3-(piperidin-1-yl)prop-1-yn-1-yl]-1,1′-biphenyl

Acta crystallographica. Section E, Crystallographic communications, 2017-06, Vol.73 (6), p.864-866

2017

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Comparison of the crystal structures of 4,4'-bis-[3-(4-methyl-piperidin-1-yl)prop-1-yn-1-yl]-1,1'-biphenyl and 4,4'-bis-[3-(2,2,6,6-tetra-methyl-piperidin-1-yl)prop-1-yn-1-yl]-1,1'-biphen-yl

Acta crystallographica. Section E, Crystallographic communications, 2015-10, Vol.71 (Pt 10), p.1132-1135

2015

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Comparison crystal structure conformations of two structurally related biphenyl analogues: 4,4'-bis-[3-(pyrrolidin-1-yl)prop-1-yn-1-yl]-1,1'-biphenyl and 4,4'-bis-{3-[(S)-2-methyl-pyrrolidin-1-yl]prop-1-yn-1-yl}-1,1'-biphen-yl

Acta crystallographica. Section E, Crystallographic communications, 2015-10, Vol.71 (Pt 10), p.1147-1150

2015

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Comparison of the crystal structures of 4,4′-bis[3-(4-methylpiperidin-1-yl)prop-1-yn-1-yl]-1,1′-biphenyl and 4,4′-bis[3-(2,2,6,6-tetramethylpiperidin-1-yl)prop-1-yn-1-yl]-1,1′-biphenyl

Acta crystallographica. Section E, Crystallographic communications, 2015-10, Vol.71 (10), p.1132-1135

2015

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Comparison crystal structure conformations of two structurally related biphenyl analogues: 4,4′-bis[3-(pyrrolidin-1-yl)prop-1-yn-1-yl]-1,1′-biphenyl and 4,4′-bis{3-[( S )-2-methylpyrrolidin-1-yl]prop-1-yn-1-yl}-1,1′-biphenyl

Acta crystallographica. Section E, Crystallographic communications, 2015-10, Vol.71 (10), p.1147-1150

2015

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Structure–activity relationship between carboxylic acids and T cell cycle blockade

Life sciences (1973), 2006-04, Vol.78 (19), p.2159-2165

2006

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Multiple Modes of α 7 nAChR Noncompetitive Antagonism of Control Agonist-Evoked and Allosterically Enhanced Currents

Molecular pharmacology, 2013-09, Vol.84 (3), p.459-475

2013

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Macrophage production of inflammatory mediators is potently inhibited by a butyric acid derivative demonstrated to inactivate antigen-stimulated T cells

International immunopharmacology, 2004-09, Vol.4 (9), p.1231-1239

2004

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Potential clinical use of butyric acid derivatives to induce antigen-specific T cell inactivation

The Journal of pharmacology and experimental therapeutics, 2000-09, Vol.294 (3), p.1146

2000

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Crystal structure of 4,4'-bis-3-(piperidin-1-yl)prop-1-yn-1-yl-1,1'-biphen-yl

Acta crystallographica. Section E, Crystallographic communications, 2017-06, Vol.73 (Pt 6), p.864

2017

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T Cell Tolerance Induced by Histone Deacetylase Inhibitor is Mediated by P21cip1

Immunopharmacology and immunotoxicology, 2005, Vol.27 (4), p.545-564

2005

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Quaternary ammonium compounds inhibit and reduce the attachment of viable Salmonella typhimurium to poultry tissues

Journal of food science, 1995-11, Vol.60 (6), p.1191-1196

1995

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Butyric Acid Derivative Induces Allospecific T Cell Anergy and Prevents Graft-Versus-Host Disease

Immunopharmacology and immunotoxicology, 2003-01, Vol.25 (1), p.13-27

2003

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Akt activation improves oxidative phosphorylation in renal proximal tubular cells following nephrotoxicant injury

American journal of physiology. Renal physiology, 2008, Vol.63 (2)

2008

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Protein kinase B/Akt modulates ncphrotoxicant -induced necrosis in renal cells

American journal of physiology. Renal physiology, 2007, Vol.61 (1)

2007

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Solid-Phase Extraction and Quantitative Measurement of Omega and Omega-1 Metabolites of JWH-018 and JWH-073 in Human Urine

Akt activation improves oxidative phosphorylation in renal proximal tubular cells following nephrotoxicant injury

Protein kinase B/Akt modulates nephrotoxicant-induced necrosis in renal cells

Acetaminophen-induced hepatotoxicity in mice occurs with inhibition of activity and nitration of mitochondrial manganese superoxide dismutase

Clinically Relevant Herb-Micronutrient Interactions: When Botanicals, Minerals, and Vitamins Collide

Hydrastine pharmacokinetics and metabolism after a single oral dose of goldenseal (Hydrastis canadensis) to humans

Drug-Organic Electrolyte Complexes as Controlled Release Systems

Cooperativity in CYP2E1 metabolism of acetaminophen and styrene mixtures

Multiple modes of α7 nAChR noncompetitive antagonism of control agonist-evoked and allosterically enhanced currents

Crystal structure of 4,4'-bis-[3-(piperidin-1-yl)prop-1-yn-1-yl]-1,1'-biphen-yl

Crystal structure of 4,4′-bis[3-(piperidin-1-yl)prop-1-yn-1-yl]-1,1′-biphenyl

Comparison of the crystal structures of 4,4'-bis-[3-(4-methyl-piperidin-1-yl)prop-1-yn-1-yl]-1,1'-biphenyl and 4,4'-bis-[3-(2,2,6,6-tetra-methyl-piperidin-1-yl)prop-1-yn-1-yl]-1,1'-biphen-yl

Comparison crystal structure conformations of two structurally related biphenyl analogues: 4,4'-bis-[3-(pyrrolidin-1-yl)prop-1-yn-1-yl]-1,1'-biphenyl and 4,4'-bis-{3-[(S)-2-methyl-pyrrolidin-1-yl]prop-1-yn-1-yl}-1,1'-biphen-yl

Comparison of the crystal structures of 4,4′-bis[3-(4-methylpiperidin-1-yl)prop-1-yn-1-yl]-1,1′-biphenyl and 4,4′-bis[3-(2,2,6,6-tetramethylpiperidin-1-yl)prop-1-yn-1-yl]-1,1′-biphenyl

Comparison crystal structure conformations of two structurally related biphenyl analogues: 4,4′-bis[3-(pyrrolidin-1-yl)prop-1-yn-1-yl]-1,1′-biphenyl and 4,4′-bis{3-[( S )-2-methylpyrrolidin-1-yl]prop-1-yn-1-yl}-1,1′-biphenyl

Structure–activity relationship between carboxylic acids and T cell cycle blockade

Multiple Modes of α 7 nAChR Noncompetitive Antagonism of Control Agonist-Evoked and Allosterically Enhanced Currents

Macrophage production of inflammatory mediators is potently inhibited by a butyric acid derivative demonstrated to inactivate antigen-stimulated T cells

Potential clinical use of butyric acid derivatives to induce antigen-specific T cell inactivation

Crystal structure of 4,4'-bis-3-(piperidin-1-yl)prop-1-yn-1-yl-1,1'-biphen-yl

T Cell Tolerance Induced by Histone Deacetylase Inhibitor is Mediated by P21cip1

Quaternary ammonium compounds inhibit and reduce the attachment of viable Salmonella typhimurium to poultry tissues

Butyric Acid Derivative Induces Allospecific T Cell Anergy and Prevents Graft-Versus-Host Disease

Akt activation improves oxidative phosphorylation in renal proximal tubular cells following nephrotoxicant injury

Protein kinase B/Akt modulates ncphrotoxicant -induced necrosis in renal cells

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