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High performance liquid chromatographic analysis of the pharmacologically active quinones and related compounds in the oil of the black seed ( Nigella sativa L.)

Journal of pharmaceutical and biomedical analysis, 1999-04, Vol.19 (5), p.757-762

1999

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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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Indirect Trapping of the Retroconjugate Addition Reaction Intermediate Involved in the Epimerization of Lobeline: Application to the Synthesis of (−)-Sedamine

Journal of organic chemistry, 2004-11, Vol.69 (24), p.8514-8517

2004

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In vitro/in vivo correlation of transdermal naltrexone prodrugs in hairless guinea pigs

Pharmaceutical research, 2005-06, Vol.22 (6), p.981-989

2005

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Physicochemical evaluation, in vitro human skin diffusion, and concurrent biotransformation of 3-O-alkyl carbonate prodrugs of naltrexone

Pharmaceutical research, 2004-07, Vol.21 (7), p.1146-1152

2004

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Lobelane analogues as novel ligands for the vesicular monoamine transporter-2

Bioorganic & medicinal chemistry, 2005-06, Vol.13 (12), p.3899-3909

2005

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Human Skin Permeation of Branched-Chain 3-O-Alkyl Ester and Carbonate Prodrugs of Naltrexone

Pharmaceutical research, 2005-05, Vol.22 (5), p.758-765

2005

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Novel antiglaucoma prodrugs and codrugs of ethacrynic acid

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (15), p.3524-3527

2005

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3D-QSAR study of bis-azaaromatic quaternary ammonium analogs at the blood–brain barrier choline transporter

Bioorganic & medicinal chemistry, 2005-07, Vol.13 (13), p.4253-4261

2005

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A duplex “Gemini” prodrug of naltrexone for transdermal delivery

Journal of controlled release, 2004-06, Vol.97 (2), p.283-290

2004

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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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Transdermal Delivery of Naltrexone and its Active Metabolite 6-β-Naltrexol in Human Skin in Vitro and Guinea Pigs in Vivo

Journal of pharmaceutical sciences, 2005-09, Vol.94 (9), p.1965-1975

2005

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Synthesis and stability of two indomethacin prodrugs

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (7), p.1874-1879

2006

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Bioconversion of Naltrexone and Its 3-O-Alkyl-Ester Prodrugs in a Human Skin Equivalent

Journal of pharmaceutical sciences, 2005-04, Vol.94 (4), p.828-836

2005

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Synthesis and evaluation of a series of tropane analogues as novel vesicular monoamine transporter-2 ligands

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (20), p.4463-4466

2005

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(Z)-2-(1-phenylsulfonyl-1 H-indol-3-ylmethylene)-1-azabicyclo[2.2.2]-octan-3-one and (Z)-(S)-2-(1-phenyl-sulfonyl-1 h-indol-3-ylmethylene)-1-azabicyclo[2.2.2]octan-3-ol

Acta crystallographica. Section C, Crystal structure communications, 2004-09, Vol.60 (Pt 9), p.o659-o661

2004

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A simple high performance liquid chromatographic method for the quantification of total cotinine, total 3′-hydroxycotinine and caffeine in the plasma of smokers

Journal of pharmaceutical and biomedical analysis, 2000-08, Vol.23 (2), p.543-549

2000

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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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The Preparation of 2-Arylmethylidene-8-methyl-8-azabicyclo[3.2.1]octan-3-ones

Synthetic communications, 2004-12, Vol.34 (11), p.1931-1942

2004

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(Z)-3-(1H-indol-3-yl)-2-(3-thienyl)-acrylonitrile and (Z)-3-[1-(4-tert-butylbenzyl)-1-H-indol-3-yl]-2-(3-thienyl)acrylonitrile

Acta crystallographica. Section C, Crystal structure communications, 2005-02, Vol.61 (Pt 2), p.o78-o80

2005

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Neuronal nicotinic acetylcholine receptor binding affinities of boron-containing nicotine analogues

Bioorganic & medicinal chemistry letters, 2001-05, Vol.11 (9), p.1245-1248

2001

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1-(1H-Indol-3-ylcarbonyl)-N-(4-methoxybenzyl)formamide

Acta crystallographica. Section C, Crystal structure communications, 2006-03, Vol.62 (3), p.o153-o154

2006

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(E)-2-Methyl-3-(2-methyl-2-nitrovinyl)-1H-indole and (E)-3-(2-methyl-2-nitrovinyl)-2-phenyl-1H-indole

Acta crystallographica. Section C, Crystal structure communications, 2005-08, Vol.61 (8), p.o527-o530

2005

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(Z)-3-(1-Methyl-1H-indol-3-yl)-2-(thiophen-3-yl)acrylonitrile

Acta crystallographica. Section C, Crystal structure communications, 2004-03, Vol.60 (Pt 3), p.o217-o218

2004

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An Improved Synthesis of β-Nicotyrine from the Dehydrogenation of Nicotine: Comparison of Conventional and Microwave-Assisted Reactions

Synthetic communications, 2003-09, Vol.33 (19), p.3305-3315

2003

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High performance liquid chromatographic analysis of the pharmacologically active quinones and related compounds in the oil of the black seed ( Nigella sativa L.)

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

Indirect Trapping of the Retroconjugate Addition Reaction Intermediate Involved in the Epimerization of Lobeline: Application to the Synthesis of (−)-Sedamine

In vitro/in vivo correlation of transdermal naltrexone prodrugs in hairless guinea pigs

Physicochemical evaluation, in vitro human skin diffusion, and concurrent biotransformation of 3-O-alkyl carbonate prodrugs of naltrexone

Lobelane analogues as novel ligands for the vesicular monoamine transporter-2

Human Skin Permeation of Branched-Chain 3-O-Alkyl Ester and Carbonate Prodrugs of Naltrexone

Novel antiglaucoma prodrugs and codrugs of ethacrynic acid

3D-QSAR study of bis-azaaromatic quaternary ammonium analogs at the blood–brain barrier choline transporter

A duplex “Gemini” prodrug of naltrexone for transdermal delivery

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

Transdermal Delivery of Naltrexone and its Active Metabolite 6-β-Naltrexol in Human Skin in Vitro and Guinea Pigs in Vivo

Synthesis and stability of two indomethacin prodrugs

Bioconversion of Naltrexone and Its 3-O-Alkyl-Ester Prodrugs in a Human Skin Equivalent

Synthesis and evaluation of a series of tropane analogues as novel vesicular monoamine transporter-2 ligands

(Z)-2-(1-phenylsulfonyl-1 H-indol-3-ylmethylene)-1-azabicyclo[2.2.2]-octan-3-one and (Z)-(S)-2-(1-phenyl-sulfonyl-1 h-indol-3-ylmethylene)-1-azabicyclo[2.2.2]octan-3-ol

A simple high performance liquid chromatographic method for the quantification of total cotinine, total 3′-hydroxycotinine and caffeine in the plasma of smokers

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

The Preparation of 2-Arylmethylidene-8-methyl-8-azabicyclo[3.2.1]octan-3-ones

(Z)-3-(1H-indol-3-yl)-2-(3-thienyl)-acrylonitrile and (Z)-3-[1-(4-tert-butylbenzyl)-1-H-indol-3-yl]-2-(3-thienyl)acrylonitrile

Neuronal nicotinic acetylcholine receptor binding affinities of boron-containing nicotine analogues

1-(1H-Indol-3-ylcarbonyl)-N-(4-methoxybenzyl)formamide

(E)-2-Methyl-3-(2-methyl-2-nitrovinyl)-1H-indole and (E)-3-(2-methyl-2-nitrovinyl)-2-phenyl-1H-indole

(Z)-3-(1-Methyl-1H-indol-3-yl)-2-(thiophen-3-yl)acrylonitrile

An Improved Synthesis of β-Nicotyrine from the Dehydrogenation of Nicotine: Comparison of Conventional and Microwave-Assisted Reactions

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