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N,N'-Alkane-diyl-bis-3-picoliniums as nicotinic receptor antagonists: inhibition of nicotine-evoked dopamine release and hyperactivity

The Journal of pharmacology and experimental therapeutics, 2008-08, Vol.326 (2), p.563-576

2008

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N-n-alkylpyridinium analogs, a novel class of nicotinic receptor antagonists: selective inhibition of nicotine-evoked [3H] dopamine overflow from superfused rat striatal slices

The Journal of pharmacology and experimental therapeutics, 2003-09, Vol.306 (3), p.1011-1020

2003

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QSAR modeling of mono- and bis-quaternary ammonium salts that act as antagonists at neuronal nicotinic acetylcholine receptors mediating dopamine release

Bioorganic & medicinal chemistry, 2006-05, Vol.14 (9), p.3017-3037

2006

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Subtype-selective nicotinic receptor antagonists: potential as tobacco use cessation agents

Bioorganic & medicinal chemistry letters, 2004-04, Vol.14 (8), p.1863-1867

2004

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bis-Azaaromatic quaternary ammonium analogues: ligands for α4β2 and α7 subtypes of neuronal nicotinic receptors

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (21), p.3067-3071

2002

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A general procedure for the enantioselective synthesis of the minor tobacco alkaloids nornicotine, anabasine, and anatabine

The AAPS journal, 2005-10, Vol.7 (3), p.E752-E758

2005

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N-n-alkylnicotinium analogs, a novel class of nicotinic receptor antagonist: inhibition of S(-)-nicotine-evoked [(3)H]dopamine overflow from superfused rat striatal slices

The Journal of pharmacology and experimental therapeutics, 2002-06, Vol.301 (3), p.1088-1096

2002

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Development of subtype-selective ligands as antagonists at nicotinic receptors mediating nicotine-evoked dopamine release

Bioorganic & medicinal chemistry letters, 2004-04, Vol.14 (8), p.1869-1874

2004

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Molecular modeling of mono- and bis-quaternary ammonium salts as ligands at the α4β2 nicotinic acetylcholine receptor subtype using nonlinear techniques

The AAPS journal, 2005-09, Vol.7 (3), p.E678-E685

2005

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N-n -Alkylnicotinium Analogs, a Novel Class of Nicotinic Receptor Antagonists: Interaction with α4β2 and α7 Neuronal Nicotinic Receptors

The Journal of pharmacology and experimental therapeutics, 2003-01, Vol.304 (1), p.400-410

2003

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N-n-alkylnicotinium analogs, a novel class of antagonists at α4β2 Nicotinic acetylcholine receptors: Inhibition of S(-)-nicotine-evoked 86Rb+Efflux from rat thalamic synaptosomes

The AAPS journal, 2006-01, Vol.7 (4), p.E922-E930

2006

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Molecular modeling of mono- and bis-quaternary ammonium salts as ligands at the alpha4beta2 nicotinic acetylcholine receptor subtype using nonlinear techniques

The AAPS journal, 2005-10, Vol.7 (3), p.E678-E685

2005

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N-n-alkylnicotinium analogs, a novel class of antagonists at alpha 4 beta 2 Nicotinic acetylcholine receptors: Inhibition of S(-)-nicotine-evoked 86Rb+Efflux from rat thalamic synaptosomes

The AAPS journal, 2005-12, Vol.7 (4), p.E922-E930

2005

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Molecular modeling of mono- and bis-quaternary ammonium salts as ligands at the alpha 4 beta 2 nicotinic acetylcholine receptor subtype using nonlinear techniques

The AAPS journal, 2005-01, Vol.7 (3), p.E678-E685

2005

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Recent developments in neuronal nicotinic acetylcholine receptor antagonists

Expert opinion on therapeutic patents, 2000-10, Vol.10 (10), p.1561-1581

2000

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N-n-alkylnicotinium analogs, a novel class of nicotinic receptor antagonists: interaction with alpha4beta2 and alpha7 neuronal nicotinic receptors

The Journal of pharmacology and experimental therapeutics, 2003-01, Vol.304 (1), p.400

2003

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A Preparative Scale Reduction of Alkyl Disulfides with Tributyl Phosphine and Water

Synthetic communications, 1999-02, Vol.29 (3), p.351-358

1999

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bis-Azaaromatic quaternary ammonium analogues: ligands for alpha4beta2 and alpha7 subtypes of neuronal nicotinic receptors

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (21), p.3067-3071

2002

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The preparation of β-substituted amines from mixtures of epoxide opening products via a common aziridinium ion intermediate

Tetrahedron: asymmetry, 1999-07, Vol.10 (14), p.2655-2663

1999

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Development of Stability-Indicating Analytical Procedures by HPLC: An Overview and Best Practices

LC GC North America, 2020-08, Vol.38 (8), p.440-455

2020

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A (1 R ,2 R ,5 R )-(+)-2α-hydroxypinan-3-one ketimine

Acta crystallographica. Section E, Structure reports online, 2005-08, Vol.61 (8), p.2682-2684

2005

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Development of Stability-Indicating Analytical Procedures by HPLC: An Overview with Best Practices

LC GC Europe, 2020-10, Vol.33 (10), p.521

2020

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N-n-alkylnicotinium analogs, a novel class of antagonists at alpha 4 beta 2 nicotinic acetylcholine receptors: inhibition of S(-)-nicotine-evoked 86Rb+ efflux from rat thalamic synaptosomes

The AAPS journal, 2006-01, Vol.7 (4), p.E922-E930

2006

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A (1R,2R,5R)‐(+)‐2α‐hydroxypinan‐3‐one ketimine

Acta crystallographica. Section E, Structure reports online, 2005-08, Vol.61 (8), p.2682-2684

2005

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ChemInform Abstract: The Preparation of β-Substituted Amines from Mixtures of Epoxide Opening Products via a Common Aziridinium Ion Intermediate

ChemInform, 1999-12, Vol.30 (52), p.no-no

1999

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N,N'-Alkane-diyl-bis-3-picoliniums as nicotinic receptor antagonists: inhibition of nicotine-evoked dopamine release and hyperactivity

N-n-alkylpyridinium analogs, a novel class of nicotinic receptor antagonists: selective inhibition of nicotine-evoked [3H] dopamine overflow from superfused rat striatal slices

QSAR modeling of mono- and bis-quaternary ammonium salts that act as antagonists at neuronal nicotinic acetylcholine receptors mediating dopamine release

Subtype-selective nicotinic receptor antagonists: potential as tobacco use cessation agents

bis-Azaaromatic quaternary ammonium analogues: ligands for α4β2 and α7 subtypes of neuronal nicotinic receptors

A general procedure for the enantioselective synthesis of the minor tobacco alkaloids nornicotine, anabasine, and anatabine

N-n-alkylnicotinium analogs, a novel class of nicotinic receptor antagonist: inhibition of S(-)-nicotine-evoked [(3)H]dopamine overflow from superfused rat striatal slices

Development of subtype-selective ligands as antagonists at nicotinic receptors mediating nicotine-evoked dopamine release

Molecular modeling of mono- and bis-quaternary ammonium salts as ligands at the α4β2 nicotinic acetylcholine receptor subtype using nonlinear techniques

N-n -Alkylnicotinium Analogs, a Novel Class of Nicotinic Receptor Antagonists: Interaction with α4β2 and α7 Neuronal Nicotinic Receptors

N-n-alkylnicotinium analogs, a novel class of antagonists at α4β2 Nicotinic acetylcholine receptors: Inhibition of S(-)-nicotine-evoked 86Rb+Efflux from rat thalamic synaptosomes

Molecular modeling of mono- and bis-quaternary ammonium salts as ligands at the alpha4beta2 nicotinic acetylcholine receptor subtype using nonlinear techniques

N-n-alkylnicotinium analogs, a novel class of antagonists at alpha 4 beta 2 Nicotinic acetylcholine receptors: Inhibition of S(-)-nicotine-evoked 86Rb+Efflux from rat thalamic synaptosomes

Molecular modeling of mono- and bis-quaternary ammonium salts as ligands at the alpha 4 beta 2 nicotinic acetylcholine receptor subtype using nonlinear techniques

Recent developments in neuronal nicotinic acetylcholine receptor antagonists

N-n-alkylnicotinium analogs, a novel class of nicotinic receptor antagonists: interaction with alpha4beta2 and alpha7 neuronal nicotinic receptors

A Preparative Scale Reduction of Alkyl Disulfides with Tributyl Phosphine and Water

bis-Azaaromatic quaternary ammonium analogues: ligands for alpha4beta2 and alpha7 subtypes of neuronal nicotinic receptors

The preparation of β-substituted amines from mixtures of epoxide opening products via a common aziridinium ion intermediate

Development of Stability-Indicating Analytical Procedures by HPLC: An Overview and Best Practices

A (1 R ,2 R ,5 R )-(+)-2α-hydroxypinan-3-one ketimine

Development of Stability-Indicating Analytical Procedures by HPLC: An Overview with Best Practices

N-n-alkylnicotinium analogs, a novel class of antagonists at alpha 4 beta 2 nicotinic acetylcholine receptors: inhibition of S(-)-nicotine-evoked 86Rb+ efflux from rat thalamic synaptosomes

A (1R,2R,5R)‐(+)‐2α‐hydroxypinan‐3‐one ketimine

ChemInform Abstract: The Preparation of β-Substituted Amines from Mixtures of Epoxide Opening Products via a Common Aziridinium Ion Intermediate

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